ZMP
ttna
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens TTN, titin (TTN) [Source:UniProtKB/TrEMBL;Acc:B0S757]
Human Orthologue:
TTN
Human Description:
titin [Source:HGNC Symbol;Acc:12403]
Mouse Orthologue:
Ttn
Mouse Description:
titin Gene [Source:MGI Symbol;Acc:MGI:98864]
Alleles
There are 113 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18062 | Nonsense | Available for shipment | Available now |
sa21585 | Nonsense | Available for shipment | Available now |
sa2497 | Nonsense | Available for shipment | Available now |
sa34748 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21584 | Nonsense | Available for shipment | Available now |
sa12924 | Nonsense | Available for shipment | Available now |
sa38761 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21583 | Essential Splice Site | Available for shipment | Available now |
sa11451 | Nonsense | Available for shipment | Available now |
sa41540 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21582 | Nonsense | Available for shipment | Available now |
sa8604 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9790 | Nonsense | Available for shipment | Available now |
sa34747 | Nonsense | Available for shipment | Available now |
sa41539 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34746 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31747 | Essential Splice Site | Available for shipment | Available now |
sa14817 | Nonsense | Available for shipment | Available now |
sa30647 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21581 | Nonsense | Available for shipment | Available now |
sa21580 | Essential Splice Site | Available for shipment | Available now |
sa16898 | Nonsense | Available for shipment | Available now |
sa15104 | Essential Splice Site | Available for shipment | Available now |
sa8690 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41538 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21579 | Nonsense | Available for shipment | Available now |
sa12471 | Nonsense | Available for shipment | Available now |
sa41537 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34745 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17286 | Essential Splice Site | Available for shipment | Available now |
sa41536 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41535 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21578 | Nonsense | Available for shipment | Available now |
sa12350 | Nonsense | Available for shipment | Available now |
sa30925 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41534 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31746 | Nonsense | Available for shipment | Available now |
sa38760 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10365 | Nonsense | Available for shipment | Available now |
sa31745 | Nonsense | Available for shipment | Available now |
sa45376 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14025 | Nonsense | Available for shipment | Available now |
sa21577 | Nonsense | Available for shipment | Available now |
sa34744 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41533 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41532 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41531 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1736 | Nonsense | Available for shipment | Available now |
sa41530 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34743 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8574 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2512 | Nonsense | F2 line generated | Not yet available |
sa21576 | Nonsense | Available for shipment | Available now |
sa1029 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa21575 | Nonsense | Available for shipment | Available now |
sa21574 | Nonsense | Available for shipment | Available now |
sa15885 | Essential Splice Site | Available for shipment | Available now |
sa34742 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45375 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9067 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18964 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11772 | Nonsense | Available for shipment | Available now |
sa41529 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16825 | Nonsense | Available for shipment | Available now |
sa13049 | Nonsense | Available for shipment | Available now |
sa41528 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16217 | Nonsense | Available for shipment | Available now |
sa45374 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34741 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41527 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13884 | Nonsense | Available for shipment | Available now |
sa12872 | Nonsense | Available for shipment | Available now |
sa21573 | Nonsense | Available for shipment | Available now |
sa45373 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa787 | Nonsense | Available for shipment | Available now |
sa14565 | Nonsense | Available for shipment | Available now |
sa13739 | Nonsense | Available for shipment | Available now |
sa34740 | Nonsense | Available for shipment | Available now |
sa15087 | Nonsense | Available for shipment | Available now |
sa2493 | Nonsense | Available for shipment | Available now |
sa21572 | Essential Splice Site | Available for shipment | Available now |
sa12142 | Nonsense | Available for shipment | Available now |
sa2492 | Nonsense | F2 line generated | Not yet available |
sa38759 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1712 | Nonsense | Available for shipment | Available now |
sa30924 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41526 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12712 | Essential Splice Site | Available for shipment | Available now |
sa25437 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21571 | Nonsense | Available for shipment | Available now |
sa41525 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41524 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18062
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 269 | 7601 | 5 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 269 | 7601 | 6 | 75 |
ENSDART00000109099 | Nonsense | 269 | 31319 | 5 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44139746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43264916 |
GRCz11 | 9 | 43066703 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACTCCACCTCGTGTGCCTCCTAAGCCAACCTCAAAATCTCCACCTTCA[C/T]AACTGACTAAAGTTTCAACTGCTCGCCAACAGTCTCCCTCTCCTGTGAGG
Long Flanking Sequence:
GAGGCCTTCCCAGAGGATTCTGGAACCTATTCTGTCAGTGCTTCTAACAGCAGCGGACGTGCAACTTCAACTGCTGAGTTGCTTGTTCAGGGTAAGAATTTTTTTTTTCACATTTTCACATTATTTTTAATAAGTGACTTAACATGCATTTCATTGGTTCACAGGTGAGGAAGAAGCCGTACCTGCAAAAAAGTCTAAAACTATAATTTCAGCCTCTCAGATATCACAAACTCGTCAGACTCGGGTGGAGAAGGTGAGTATCAGTTGCAACAGTGAACGAGCCTTCACAACTCTCTTGAGAGTATCACAGTAAAGTCTCATTTACCTCTATGATCATTGTGTTAATTGCTTTTTTTTTATTCTGACAGAGAGTGGAAGCTCGTTTTGAGGCCACTGCCACAATGCAAATGCAGGTTGAAAGTGGAGTTGTTACAGAACATCTGGCACATAAGACTCCACCTCGTGTGCCTCCTAAGCCAACCTCAAAATCTCCACCTTCA[C/T]AACTGACTAAAGTTTCAACTGCTCGCCAACAGTCTCCCTCTCCTGTGAGGCATGTTAAGGGCCCGACACCCACTCCTGTCAGGTAACGTGTCTGAAGTTTTCTGAATCACATCACATCTTTTGACAATTAATATAGTACATTTCACTGGGCTTGAATACTTATGTTAATTTAATGGAAGCATTAAAGGGATATTTTCAAAATAATAAACTTGAAGTGATACACCTTTTTGGTCATAATTGCTAACAAAATAAAATAAATGTTGTTTTGGAATAAAAATTGCCACTATTTTTGTTTGTTAACATGCATTGCTATTATTGATGTAAACATTTAATCCCTGCAAGTTTCTATTTTCTTTTTTCTTGGTTGTCTAAAATAAAAATCTGAAAAAGATGTATATTGTAGAGCTGTTTATATTAATTAATAATTAATAATAATTCCTGACATTAATATAGCATTTTTTATGGACACTCAAAATGCTTTACACATTGGGGAATCTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21585
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 429 | 31319 | 8 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44135989)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43261159 |
GRCz11 | 9 | 43062946 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTAAGCAACAATTTAGAGGTTTCTTTCCACATGTTCATAGATATCATG[T/A]CAGGGAATCCAGGAGAAATCTGTGACAACTCAAACTTTGACAACTCATAA
Long Flanking Sequence:
GTTTTCATTTTTTGCATGTTACAGATGTCTCTCCACAGGATTCTATCTTACAAACTGTTTGTTTCTCAGTGAAATTGTATGTCCTGTTAAGTTTGACAACATCTTGCAACCTCAATTCTACTTGCATGTATAAAGGAGCAGCAAAACACGGATGAGAAAAGTGTTGCTGTTGCCACTGTAGTGGCGGCAGTGGACCATGCTCGTAGTCGTGGACCACTCAGCGACTATGTAGAACAGCCCAGTGTTGAAACCGGCATAACTGCAGTACACATTACATCTCAAAATGAGCAGGTAGTTTGGTAGTGCTGTGGTCGTCACCCATCCAAACTTCATACTCCTATTTACCCCAACTGACTCCACATAGATTTTTAATAGCCAACCATAACAACTTTTACTCGCAATTTTCCCCCAACCCATTACTTTATTCTTGAACATAAACTTATTTTTCTTTATTAAGCAACAATTTAGAGGTTTCTTTCCACATGTTCATAGATATCATG[T/A]CAGGGAATCCAGGAGAAATCTGTGACAACTCAAACTTTGACAACTCATAAAATCAGTATTGATGTTTCAACCACTAGTGAGAGATCCTTGGAAAAGATCGAAGCAACTGCAGAGGTAGAGTCTAGGATAATAAATTATACTTGGCCACAATAATAATTTTTTTTCTATGCACTTTTGTTAAAGAGCACCTTCTGTTTTTGTGTTTAAGGGCAACATTTAAAAGGCTGCATATATTCAGCTATGGATAGTTTGAAAAATGTAATAAAGTTTGATTGAACTTAAAAAATCTGCAACTTCATTGCCTTTCTAACCATTTTTAGTTGTTAATAAAATGTTAATAAAAAATTAGGGCTGTATGGTATTGGAAAAATTCCCAGAGATGGGTTTTTTTAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACACCGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATGATATTGGAAAAATCTGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2497
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 786 | 7601 | 12 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 786 | 7601 | 13 | 75 |
ENSDART00000109099 | Nonsense | 1179 | 31319 | 20 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44126752)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43251922 |
GRCz11 | 9 | 43053709 |
KASP Assay ID:
554-2866.1 (used for ordering genotyping assays)
KASP Sequence:
AACTCTATGTGGAGTCCACTGCTGCTGCTCAGCCTTACTATCCTCAGGCT[G/T]AAGCTGTGAGGAGAGTCCAGTGAGTTTTCTTYACCTTACCAAGCTTCATC
Long Flanking Sequence:
TCCAAGAAATTGAAATCCGCATCCTTAAAATTACTTACCAAGAGCTGGTGATTGAGGACGGAGAGGAGATGGTCATAAATGTTGCTGAGCATGAGGCCGTTGCATCTTCATTTAGCACTCCTGTGAAAAGCTACAGAATTCTTGAAGGAATGGGTGTTACTTTCCATTGCAAAATGGGAGGAAAACCATTACCAAAGGTAATAATGCTAAATCAATTAAAAACAGTATTCGCACAGCAGCACAATGTATGCTAGTAATTATGCATGTTTTGTGATAAATAGATTGCCTGGTACAAAGACGGCAAGCGTATAAAGCATGGAGGACGCTACCAGATGGAGGTTTTACAAGATGGTAGAGCCAGTCTGCGTCTGCCTGTGGTGCTGCCAGAAGATGAGGGCATCTATACTGCATTTGCCAGTAATATGAAGGGTAATGCTGTCAGTTCTGGAAAACTCTATGTGGAGTCCACTGCTGCTGCTCAGCCTTACTATCCTCAGGCT[G/T]AAGCTGTGAGGAGAGTCCAGTGAGTTTTCTTCACCTTACCAAGCTTCATCTCTATATTTGTAATTCTATGACTATAAAATGTTTAAGGTAATATTCCACACCTATGTTGACACTTTTAGGTCCACATCTCCAATGTCTGCTCGCTCAGCCAGCTACTCCCCTGGACGTTCTCCTGCTCGCTCTGTTAGCCGATCTCCTGCACGTAGACTTGATGACACGGACGAGAGTCAACTGGAAAGGCTTTATAAGCCTGTTTTTGTACAAAAGCCCTCTTCCTTCAGGTGTTCTGAAGGACAGACAGCAAGGTTTGACTTAAAAGTAGTTGGAAGACCTATGCCCGACACTTTCTGGTTCCACAGTGGTAAGTGTGTTTCAGAGCTGTTCCACCATTCCAAAATTTAGGATTTGATATTTGTGCTTAATTTATGGTTGATATCTTTATAGTGCTGAAAAGAATTAATCTCTTTTAAATTTTCTATTTAAGGACAACAAGTGGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34748
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 869 | 7601 | 13 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 869 | 7601 | 14 | 75 |
ENSDART00000109099 | Nonsense | 1262 | 31319 | 21 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44126401)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43251571 |
GRCz11 | 9 | 43053358 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAGGTTTGACTTAAAAGTAGTTGGAAGACCTATGCCCGACACTTTCTG[G/A]TTCCACAGTGGTAAGTGTGTTTCAGAGCTGTTCCACCATTCCAAAATTTA
Long Flanking Sequence:
GTAGAGCCAGTCTGCGTCTGCCTGTGGTGCTGCCAGAAGATGAGGGCATCTATACTGCATTTGCCAGTAATATGAAGGGTAATGCTGTCAGTTCTGGAAAACTCTATGTGGAGTCCACTGCTGCTGCTCAGCCTTACTATCCTCAGGCTGAAGCTGTGAGGAGAGTCCAGTGAGTTTTCTTCACCTTACCAAGCTTCATCTCTATATTTGTAATTCTATGACTATAAAATGTTTAAGGTAATATTCCACACCTATGTTGACACTTTTAGGTCCACATCTCCAATGTCTGCTCGCTCAGCCAGCTACTCCCCTGGACGTTCTCCTGCTCGCTCTGTTAGCCGATCTCCTGCACGTAGACTTGATGACACGGACGAGAGTCAACTGGAAAGGCTTTATAAGCCTGTTTTTGTACAAAAGCCCTCTTCCTTCAGGTGTTCTGAAGGACAGACAGCAAGGTTTGACTTAAAAGTAGTTGGAAGACCTATGCCCGACACTTTCTG[G/A]TTCCACAGTGGTAAGTGTGTTTCAGAGCTGTTCCACCATTCCAAAATTTAGGATTTGATATTTGTGCTTAATTTATGGTTGATATCTTTATAGTGCTGAAAAGAATTAATCTCTTTTAAATTTTCTATTTAAGGACAACAAGTGGTAAATGACTACACTCACAAGATTGTGGTGAAAGAGGATGGAACTCAGTCAATGATTGTCGTTCCTGCCATGCCTCAGGACTCTGGAGAGTGGACAGTTGTTGCTCAGAACAGAGCTGGAAAGACAACTGTTTCTATGACTCTCACTGTTGAAGGTAACCTTCTGTTGTTTTTCTGAAAATATTAACAGCTACGCTTGGTTGTGTTGCAGATTGTATAAACTCATGTATTTTACATTACAGCAAAAGAGAATTTAGTTCGACCTCAGTTCATTGAAAAACTGAAGAATATCAGTGTTAAAGAAGGAAGTCTGGTTGAGTTGGCAGTAAAAGCCATTGGAAACCCCCTGCCTGACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21584
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 1192 | 7601 | 16 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 1192 | 7601 | 17 | 75 |
ENSDART00000109099 | Nonsense | 1585 | 31319 | 24 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44125142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43250312 |
GRCz11 | 9 | 43052099 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGAAGAGTCTGGTAGAGGACAGTCAATTACCAGAAGGAAGAAAGGTA[C/T]AAAGAATGGATGAAATGGAGAGAATTGCCCATGAGGGTGGACCCTCTGGA
Long Flanking Sequence:
ATGTGGAGGTAGAATACACTGAACCTGTACCAGAGAGAAGACTTATCATCCCCAAAGGGACATATAAGGCTAAGGATGTTGCACCACCAGAGATTGAACCACTGCATCTTCGCTATGGTCAGGAGCAGTGGGAAGAGGGTGACCTCTATGACAAAGAAAAGCAACAGAAGCCACACTTTAAAAAGAAACTTACTTCAGTCCGGATGAAGCGGTTTGGACCTGTGCACTTTGAATGCAGACTTACCCCTATTGGTGACCCTACAATGGTTGTTGAATGGCTCCATGATGGCAAACCACTCGAAGCTGCTAACAGACTTCGGATGATCAATGAGTTTGGCTATTGCAGTCTTGATTATGAAGTTGCTTATTCCAGAGATAGTGGTGTCATTACTTGCAGAGCTACAAACAAGTTTGGTGCCGACCAAACCTCTGCCACACTAATTGTGAAGGATGAGAAGAGTCTGGTAGAGGACAGTCAATTACCAGAAGGAAGAAAGGTA[C/T]AAAGAATGGATGAAATGGAGAGAATTGCCCATGAGGGTGGACCCTCTGGAGTAACTGGGGATGACATGTCTGAGAAGTCCAAGCCAGAGATTGTCTTACTCCCTGAACCAATAAGAGTATTTGAAGGCGAGACAGCCAAATATCGATGCAGAGTGACTGGTTACCCCACTCCCAAAGTTAATTGGTACCTTAATGGTCTGCTCATTCGAAAGAGCAAACGATTCAGACTACACTATGATGGCATTCACTATTTGGAAATTACTGACTGTAAGTCCTATGATTCTGGAGATGTCAGAGTATTGGCTGAGAACCCAGAGGGTACAGCTGAGCATACTGTCAAGCTGGAAATTCAACAAAAGGAAGATTTCAGGACAATCTTGCGCCGTGCTCCTGAGCTGAAGGCTCCAGAGGCACCTGGCCCTGAACCGGGCAGAGTATCCTTTGATGTTGTAAAGGTAGATAAACCCACAGATGCTTCTCAAGCAAAAGAAGTTGTCCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12924
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 1227 | 7601 | 16 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 1227 | 7601 | 17 | 75 |
ENSDART00000109099 | Nonsense | 1620 | 31319 | 24 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44125037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43250207 |
GRCz11 | 9 | 43051994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGGGATGACATGTCTGAGAAGTCCAAGCCAGAGATTGTCTTACTCCCT[G/T]AACCAATAAGAGTATTTGAAGGCGAGACAGCCAAATATCGATGCAGAGTG
Long Flanking Sequence:
ATCTTCGCTATGGTCAGGAGCAGTGGGAAGAGGGTGACCTCTATGACAAAGAAAAGCAACAGAAGCCACACTTTAAAAAGAAACTTACTTCAGTCCGGATGAAGCGGTTTGGACCTGTGCACTTTGAATGCAGACTTACCCCTATTGGTGACCCTACAATGGTTGTTGAATGGCTCCATGATGGCAAACCACTCGAAGCTGCTAACAGACTTCGGATGATCAATGAGTTTGGCTATTGCAGTCTTGATTATGAAGTTGCTTATTCCAGAGATAGTGGTGTCATTACTTGCAGAGCTACAAACAAGTTTGGTGCCGACCAAACCTCTGCCACACTAATTGTGAAGGATGAGAAGAGTCTGGTAGAGGACAGTCAATTACCAGAAGGAAGAAAGGTACAAAGAATGGATGAAATGGAGAGAATTGCCCATGAGGGTGGACCCTCTGGAGTAACTGGGGATGACATGTCTGAGAAGTCCAAGCCAGAGATTGTCTTACTCCCT[G/T]AACCAATAAGAGTATTTGAAGGCGAGACAGCCAAATATCGATGCAGAGTGACTGGTTACCCCACTCCCAAAGTTAATTGGTACCTTAATGGTCTGCTCATTCGAAAGAGCAAACGATTCAGACTACACTATGATGGCATTCACTATTTGGAAATTACTGACTGTAAGTCCTATGATTCTGGAGATGTCAGAGTATTGGCTGAGAACCCAGAGGGTACAGCTGAGCATACTGTCAAGCTGGAAATTCAACAAAAGGAAGATTTCAGGACAATCTTGCGCCGTGCTCCTGAGCTGAAGGCTCCAGAGGCACCTGGCCCTGAACCGGGCAGAGTATCCTTTGATGTTGTAAAGGTAGATAAACCCACAGATGCTTCTCAAGCAAAAGAAGTTGTCCGACTGAGGAAAGCTGAGAGAGTGGTTCATGAAAGGTCTACAGAAGAAACAGAAGAGCTGCGAAGCAAATTTAAGCGCAGGACTGAAGAGGGCTATTATGAAGCCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38761
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 1507 | 7601 | 16 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 1507 | 7601 | 17 | 75 |
ENSDART00000109099 | Nonsense | 1900 | 31319 | 24 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44124195)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43249365 |
GRCz11 | 9 | 43051152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTTAAAAATGGCATTTTACTTGAGAAGTCAGATCGGGTTTATTGGTA[T/A]TGGCCTGAAGATCATGTCTGTGAATTAGTAATCAGAGATGTCTTAGCTGA
Long Flanking Sequence:
GTTGTAAAGGTAGATAAACCCACAGATGCTTCTCAAGCAAAAGAAGTTGTCCGACTGAGGAAAGCTGAGAGAGTGGTTCATGAAAGGTCTACAGAAGAAACAGAAGAGCTGCGAAGCAAATTTAAGCGCAGGACTGAAGAGGGCTATTATGAAGCCATATCTTCTGTTGAATTGAAGTCTCGCAGGAAAGATGAGTCTTATGAAGGAATGCTAAAAAAGAGAAAGGAAGAACTTCTGCACTGGACCAAAGAGGTCTCTGAGGCAGAAAAGAAGAAAGAGGAAGAGGAACGCAAACTTACCATTCCTACAATCAGACCCGAGAAAGTTGCACTCTCTCCTAGCATGGAGGCTCCGAAGATCTTGGAAAGAATTCAGAGCCAGACAGTTGCTCTTGCTGATGAAGTACGCTTTCGATGTAGGGTAATTGGTAAACCAGATCCAGAGTGCCAGTGGTTTAAAAATGGCATTTTACTTGAGAAGTCAGATCGGGTTTATTGGTA[T/A]TGGCCTGAAGATCATGTCTGTGAATTAGTAATCAGAGATGTCTTAGCTGAAGACTCTGCCAGTATCATGGTCAAAGCCATTAACATTGCCGGTGAGGCCTCAAGCCATGCCTTCTTGTTGGTGCAAGGTAAGTATTGTTATGTTTAAATCAGTCTTACGCTAATGATCAATATTACTTCATCTAATGAATTCTGTCTTGCTTTTTGCAGCCAAGCAAGTTGTATCTTTTACCCAAACACTGGAGGATGCCTATGCTAAAGAGAAAGACACAATGGTAACCTTTGAATGTGAGACAAATGAGCCATTTGTCAAGGTTAAATGGATGAAGAACAATGCTGAAATCTTTTCTGGAGACAAATACAGGATGCACTCAGACAGAAAAGTTCACTTTCTGTCTGTGCTGATAATCAACATGCAAGATGATGCAGAGTACAGCTGTGCTGTAGTTGATGATGACCACATAAGAACCACTGCCAGACTTTATGTTGAAGGTCAGCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21583
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Essential Splice Site | 1550 | 7601 | 16 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Essential Splice Site | 1550 | 7601 | 17 | 75 |
ENSDART00000109099 | Essential Splice Site | 1943 | 31319 | 24 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44124066)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43249236 |
GRCz11 | 9 | 43051023 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAACATTGCCGGTGAGGCCTCAAGCCATGCCTTCTTGTTGGTGCAAGG[T/G]AAGTATTGTTATGTTTAAATCAGTCTTACGCTAATGATCAATATTACTTC
Long Flanking Sequence:
AGGACTGAAGAGGGCTATTATGAAGCCATATCTTCTGTTGAATTGAAGTCTCGCAGGAAAGATGAGTCTTATGAAGGAATGCTAAAAAAGAGAAAGGAAGAACTTCTGCACTGGACCAAAGAGGTCTCTGAGGCAGAAAAGAAGAAAGAGGAAGAGGAACGCAAACTTACCATTCCTACAATCAGACCCGAGAAAGTTGCACTCTCTCCTAGCATGGAGGCTCCGAAGATCTTGGAAAGAATTCAGAGCCAGACAGTTGCTCTTGCTGATGAAGTACGCTTTCGATGTAGGGTAATTGGTAAACCAGATCCAGAGTGCCAGTGGTTTAAAAATGGCATTTTACTTGAGAAGTCAGATCGGGTTTATTGGTATTGGCCTGAAGATCATGTCTGTGAATTAGTAATCAGAGATGTCTTAGCTGAAGACTCTGCCAGTATCATGGTCAAAGCCATTAACATTGCCGGTGAGGCCTCAAGCCATGCCTTCTTGTTGGTGCAAGG[T/G]AAGTATTGTTATGTTTAAATCAGTCTTACGCTAATGATCAATATTACTTCATCTAATGAATTCTGTCTTGCTTTTTGCAGCCAAGCAAGTTGTATCTTTTACCCAAACACTGGAGGATGCCTATGCTAAAGAGAAAGACACAATGGTAACCTTTGAATGTGAGACAAATGAGCCATTTGTCAAGGTTAAATGGATGAAGAACAATGCTGAAATCTTTTCTGGAGACAAATACAGGATGCACTCAGACAGAAAAGTTCACTTTCTGTCTGTGCTGATAATCAACATGCAAGATGATGCAGAGTACAGCTGTGCTGTAGTTGATGATGACCACATAAGAACCACTGCCAGACTTTATGTTGAAGGTCAGCTTACACTTATTCTCATTTGTTGCTTTTTATTAAAATTTTTTAAAGTCATCTCTGAATGTCTTTTTCACATGTGCTGTCTGATTTGTCACACAGGTGCACCACTGGAAATTGTTAAAAATCTTGAGAGCGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11451
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 2048 | 7601 | 22 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 2048 | 7601 | 23 | 75 |
ENSDART00000109099 | Nonsense | 2441 | 31319 | 30 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44122030)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43247200 |
GRCz11 | 9 | 43048987 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGGCTTAAGGATGGCCACTCTGTTGACTTCAGTGATATTGTCAGGAGT[G/T]AGGATATAGATGCTGTCCGTCGACTTATTTTTGTTATCACAAGAYCTCAG
Long Flanking Sequence:
TTTTTCATACAGAGGTCAGCATCATCAAGCACATGGAGGACTGTGTGTGCACAGAAACTCAGAATGTCACATTTGAAGTTGAATTATCACACACTGGTATAGACGCTTATTGGACCTTCAAGAATCAGCCTCTCAAGGCTGGCCCCAAATACAAAATTGAGTCCAAAGGAAAGCACTACAGTCTGACCATCATCAATGCCATGAAGGATGAAGAGGGCTTGTATGCATTTGCAGCAGGAGAAAAGATTTCCAGTGCAAAACTAACTGTGTCAGGTATGAGTTTTAGCATTTGCGCAAATATGTGTTTAGTTGATAAACAGATACTGCCTAATGCTTGCAATTTTTGTACACTAGGTGGTGCTATAAACAGACCACTCCATGATGTGACTGTAGCAGAATCCCAAACTGCTGTTATGGAGTGTGAGGTTGCTAATCCTACATCTGAAGGCAAGTGGCTTAAGGATGGCCACTCTGTTGACTTCAGTGATATTGTCAGGAGT[G/T]AGGATATAGATGCTGTCCGTCGACTTATTTTTGTTATCACAAGACCTCAGGATATTGGAGAGTACACATACCAAGTGGCAAATTCCAAGACATCTGCCAACCTAAGAGTTGAAGGTACTTGTACTGCCATGTTTTGAATAGTTATGTCCTTTTCAACATTTATTATTTGCAACTGATTACAACTGTGTCTTTCACAGCTGTGAAGATCAAGAAGACACTCAAGAACCAAACAGTCACAGAAACTCAAGAGGCAGTGTTTAGTCTTGAACTCACTCATTTAGATGTGAAAGGATCCCAGTGGATCAAGAATGGAGTAGAAATTGAACCTAGTGACAAATATGAGATTACAGTAGATGGATTAGTTCACACTTTAAAGATCAAGAACTGCAACTCTCAAGATGAATCAGTTTATGGATTCAAACTGGGAAAACTGTCTGCTAATGCCAGACTGAATGTCGAAAGTAAGTGTAATATTTGGCAAAATCAAAAATAGCTTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41540
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Essential Splice Site | 2347 | 7601 | 25 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Essential Splice Site | 2347 | 7601 | 26 | 75 |
ENSDART00000109099 | Essential Splice Site | 2740 | 31319 | 33 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44120873)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43246043 |
GRCz11 | 9 | 43047830 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCTTTGTGTGTGGAAATGACAAAGTCTCAGCCACCTTGACAGTCAGCC[G/T]TAAGTTCATTTTTATTTGATTTTTTAATGCAAAATTGTTTACCTGGATAT
Long Flanking Sequence:
TTCAAAAACCAAGAGCTGAAACCTAGTGCTAATGTTCAGATAATGTCTGAAAGGAAAGCACATAAGTTGGTTATTCAGAATGTTGAAGAAAGCAATGATGGAGAATACACAGCCGTTGTTGGACATTTACAATGCAGTGCATATTTGCATGTTGAATGTAAGTATGAATGTAAAGATTTAACTAATCAAACTTGTTTATTGCCTACCACACTGCTGACTCTATATCATGACTGTTTCAGCTTTGAGAGTCACAAAACCCCTAAAGAACCTTGAGGTTCCAGAGACCCATGTGGCCACATTTGAGTGTGAAGTTTCACACTTCAATGTTCCGTCCACCTGGCTGAAAAATGGAGTTGAGATCGAGATGAGTGAGAAGTTCAGAATTGTGGTGCAGGGCAAACTTCATCAGCTGAAGATCATGAATACCAGCAGAGATGATTCTGCAGAATACACCTTTGTGTGTGGAAATGACAAAGTCTCAGCCACCTTGACAGTCAGCC[G/T]TAAGTTCATTTTTATTTGATTTTTTAATGCAAAATTGTTTACCTGGATATGCTTTTATTAAAACTTAAATAATAACAACAATGGTAAAAAAAGGTAAACATGATTTAAAAATATGAATTCAGCACATGTTTCTTCCTTCTCTTCCAGCTGTGCTGATTACATCTATGCTCAAAGACCTGAATGCACAAGAAAAGGACACCATCACATTTGAGGTGACCGTCAACTATGAAGGCATCACTTACAAATGGCTGAAGAATGGAGTAGAAATAAGATCCAGTGATAGATGTCAAACTCGCACTAAACAGCTCTCTCACTCCCTCACCATTCGGAATGTTCACTTTGGGGATGTTGGAGACTACAAATTTGTGGCTGGATCTGCTGAAACAGCAGCAAAATTGTTTGTTGAAGGTAACACTAGCTTTTTTATGAAATTATTATTCTTATTTTTTTATGGGTAATTTGGTTGATTCTGATCAAGTTGTTTTATTATGATCAATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21582
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 2483 | 7601 | 28 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 2483 | 7601 | 29 | 75 |
ENSDART00000109099 | Nonsense | 2876 | 31319 | 36 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44120129)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43245299 |
GRCz11 | 9 | 43047086 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATTAAAAGTAGCATCCTGATGGATACATAATCTTCACGTTTTAGGTA[C/A]AAGGTCTCCACAGAGAGACACGTGCATCGTCTCATGATCCAAACTGTGCG
Long Flanking Sequence:
AATGGCTGAAGAATGGAGTAGAAATAAGATCCAGTGATAGATGTCAAACTCGCACTAAACAGCTCTCTCACTCCCTCACCATTCGGAATGTTCACTTTGGGGATGTTGGAGACTACAAATTTGTGGCTGGATCTGCTGAAACAGCAGCAAAATTGTTTGTTGAAGGTAACACTAGCTTTTTTATGAAATTATTATTCTTATTTTTTTATGGGTAATTTGGTTGATTCTGATCAAGTTGTTTTATTATGATCAATTTAAGCTCGAGTCATTGAGTTCACCAAGCACATCAAGGACATTAAAGTCACTGAGAAGAAAAAGGCTGTTTTTGAATGCGAACTCTCTGAGCCTAATGTCCAAGTAACATGGATGAAAGATGGTCAGGAGCTTGAATTATCTGAGAGGTATATAACGGTTTTCCATATTAATCAAAATTTTGCTCTTTGACTTTAGTATATTAAAAGTAGCATCCTGATGGATACATAATCTTCACGTTTTAGGTA[C/A]AAGGTCTCCACAGAGAGACACGTGCATCGTCTCATGATCCAAACTGTGCGCATGTCTGATGCTGGTGAATACTCTGTGGTTGCTGGATCCAGTGTATCAAAGGCCAACCTCACAGTTGAGGGCAAGGATGTGCGCATCAGTGAGCCTGCAGAGAAAGAAATTACTGTAAGTATAAAGCTGTATTAGATATTTAAAATAATGCCCAACAGTAGTATTAGTCATTAGGGATTAATTAATTTCCATTTTAAATCACAATTTTAATGCAGGTTCTTGAGAAACAGAGAAGTACATTTGAATTCGAAGTCAATGAGGATGACATTGAAGGTCGTTGGCTAAGAAATGGAGTGGAGATCCAGTTTTCTGTTGATCAGCGCTTTAACTATGCCATTATTAGAAAAATCCATCGCTTGACAATCACAGAAACGTACAGAAGTGATGCAGGAGAATACACATTCATTGCTGGAAAGAACCGGAGTATTGTGACCCTGCATGTGAACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8604
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 2689 | 7601 | 30 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 2689 | 7601 | 31 | 75 |
ENSDART00000109099 | Nonsense | 3082 | 31319 | 38 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44119157)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43244327 |
GRCz11 | 9 | 43046114 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAATGAGCAYACATTGCTGCTCATCGAAGTCTTCCCWGAAGATGCAGCT[C/T]AGTATAACTGTGAAGCTAAGAATGACTATGGAGTTGCCACAAGCTCAGCT
Long Flanking Sequence:
GGAGTATTGTGACCCTGCATGTGAACAGTAAGTTTGATCTTGGAAGGTTTAGTGCAAACTGTTAATATGTTAATACTAACTTTTCTACGGTATGTTATTTATTTGCACTTACATTAAATGAAATTAACAACTTTATAAAAGACATTCATTAAAATAAATATATTCTATTAGATATTTTAAAGCCCTAACATGTTTTGTAGATGCTTTCATGGTGTCGTCTTGTATGGGATATACATTTGTTGTTTACAACTTATTCTCATACAACATTATTGCATTGTTTAGTCCCTGAGCCTCCTCAGATCATCAGGCACATGCAGCCCCTGTCTGTTGAAGCTGGCAAACCTGCACGCTTCTCTGTGGAGGTGACTGGAATTCCTCAGCCTCAAGTGTCTTGGTATAAGAACTCCCAGGCCCTGTCCTCTGGATTCAAGTGCAAGTTCCTGAGGGAGGGAAATGAGCATACATTGCTGCTCATCGAAGTCTTCCCAGAAGATGCAGCT[C/T]AGTATAACTGTGAAGCTAAGAATGACTATGGAGTTGCCACAAGCTCAGCTTCACTAAATGTTGAAGGTAAAGAAAATCAAAAAAAAAAAAAAAATCACATTAATAATTATTTGTAAATGTTTTAATTATACTCGTCTTTTAATCCTCAGTTCCAGAAGTTGTTTCCCCTGACACTGGAGCACCACTGTCACCTCCCGTGGTCTTAACACCAATACAAAATACTTCTGCCAATGAAGGACAATCTGCTAGATTCCAGTGCAGAGTCTCAGGAGAAGGTAAAGTCAAAAACTAATAACCAAAACCTTTCTGCCTATTTTCCATGTCAACAACTGTTTTATAAGTTAGTTCTTCAGAGGCTCCAGATCAATTGCTCTTGTAAACTGTATATAGGTGACCTTTATTTCTGTAGTCCTATATACAGTTAAAATAAAGCAGTTTCACATAGATCCACAGAAAATGTTTAGTAAAAACTATTGGAAACTGGCTATGGAAACAAATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9790
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 2947 | 7601 | 34 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 2947 | 7601 | 35 | 75 |
ENSDART00000109099 | Nonsense | 3470 | 31319 | 43 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44105613)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43230783 |
GRCz11 | 9 | 43032570 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGAGAGAGATGAATACTCTTTAATAATAACAAAAGTCAAGAAAGATTA[T/A]GAAGGAGAGTATTCTTGTACTGCAAGTAATAGATTTGGCCAGACTACCTG
Long Flanking Sequence:
AAATCAAACTGTTTACTCTTGTTCTGACATTATTTCTTAATCTAAGGGGCATTGTTATGTCCGCTTCTTGATTAGTACTGACTGATTATCATGTTTATCTTTCTTGTAGTTTATGAGACATTTTGGAGAAATCTTTAATCCCATTATTTTTATACAGAATTTTCTAGTTTGACTGTGAAGACCGAAGAAGAGGAAGAAACCTACAGCACATCACTGCATTTGCCTGAAAAATCAAAAACACTTGAACTTAAGCCAGAGCAAAAACGTTTTTCTAGTTCTTTGGAAAGAAAAAGAGAGAAACCAGTATTTGAGTCAAAGCTTACACCTGCTGAAGTTACTATTGGAGAGTCGGTTAGGTTTACTGTCACAGTATCTGGTTTTCCAAAGCCAAAGGTTCAGTGGTTTCACAATGGAAAGGCTATCACTTCATCATCAATTTATACGTTTGTAGAGGAGAGAGATGAATACTCTTTAATAATAACAAAAGTCAAGAAAGATTA[T/A]GAAGGAGAGTATTCTTGTACTGCAAGTAATAGATTTGGCCAGACTACCTGCAAGACAATATTAAAGGTAGAACTGAGTCAGTTATCAGCAGCAGAAAAGTGGGTGGAAAAAATGTTCAAAATACCAGGACAACCTCCATGCTTTACTACACAAATCCAACCTGTTCAGTGTGTGGAAGGTAGCGAGGTAAAATTTCTGTATAAAGTTACTGGTACACCATTTCCTGATGTTCAGTGGTTTAAGGGCAATTCTCAAATTAAGTCAAGCCAGACCTGTTCTGTTGTGTGCAATCCAGATGGCTCTGGCTTCCTTATTATGAGTAATATTCAACAGAGAGACAGTGGACTCTACACATGCAAGGCTGTCAATCCTTTTGGGGAGGCAAGCTGCAGTGCTGAGTTGATTGTATTCCACAAACAAGTCTCTGTGTTTCATAAACAACAATTAGTTCAAGAACAAAAAAGTTACAAGGTGTCGATGAAAGAGGAAGCCACCGAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34747
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 3329 | 7601 | 34 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 3329 | 7601 | 35 | 75 |
ENSDART00000109099 | Nonsense | 3852 | 31319 | 43 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44104469)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43229639 |
GRCz11 | 9 | 43031426 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAAGAGGGAGTTAAAATTCTTTACAGTGCAGTTTCATCAGAGAAACAA[C/T]AGTTTACAGAGGGTCACTCTAAAGAACTATCAACAGAAGAACCAACTTTT
Long Flanking Sequence:
TTGCAACCGTGCACAAAGAGCAGGTGACTCATCAAGCTGCTTTGCTGCAGTCTCATGAAGTGCAGGAGAGAGTAATATCAGCTCAAGTTCGCCCAGAACCAGTGGTAGCAACTCCTTTGAGACAGCTCCAAATGGCCACTATGACCTCCGCAGTTCAAGAAAGCCAAGGCTTCACAGAACAGCACTTTGAACGAATCAAAAGTCCTGAGGTTACAGAGATACAAATTGCCAAAGAGCACCCATCGCAAGTAATGTCTGCCTTAACTGAGAGTGTAACTCCATTAACGATTGTCAAAGCAGAGCCATTATCCACTTTAGAAACAGAAAAGATTAAGGCATCTCCTGAGCCCAAGTATCCAATATCAAGTCACCAAGTTGAGACAAAGCTCCCAATTGTTAAAGAACATTCAGAGGTTATACCCCATACTCAGCAAGAAAAGGGTTATCAAGTTAAAGAGGGAGTTAAAATTCTTTACAGTGCAGTTTCATCAGAGAAACAA[C/T]AGTTTACAGAGGGTCACTCTAAAGAACTATCAACAGAAGAACCAACTTTTCAGACATCGGTGAAAAAAGAACAACACAAACCGGTTGTACTTTCAGTTAATGAGACAACTCAGACCTTATCTAAGGAAGAGAGCTTATCAGTGCAGAAACCAGGTGTTGAGACTGCATCTCAAGTGAAAGACAGTGTCTTTAAATCAGCTCTTGTTGCTGAGGAAAAGCATCAGCTCCAAGCTGATCAGTCAAGTTTGATTCCAGGTTTAGACAGTGCAATTTCAGTGCAACCCCTAAGAGAAGAAGAACAAGTTCAACATTTGCAAGTTATCACAGATCAAGGTATTCTTCCAGCTGAAGGAAGGTTTAGCAGTGAGAACCCAAGCCCAGAGAAAGCAGATGCTCAAAAAAGTCCTCTACTTAAGCATACAGTGTCAGTGGATTTACAGCAGACAGTGACATGTGAGGAGTCCTCAGAGTTTTCAGGACAAGTAACAGAGCTTTCTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41539
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 3353 | 7601 | 34 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 3353 | 7601 | 35 | 75 |
ENSDART00000109099 | Nonsense | 3876 | 31319 | 43 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44104397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43229567 |
GRCz11 | 9 | 43031354 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAACTATCAACAGAAGAACCAACTTTTCAGACATCGGTGAAAAAAGAA[C/T]AACACAAACCGGTTGTACTTTCAGTTAATGAGACAACTCAGACCTTATCT
Long Flanking Sequence:
TAATATCAGCTCAAGTTCGCCCAGAACCAGTGGTAGCAACTCCTTTGAGACAGCTCCAAATGGCCACTATGACCTCCGCAGTTCAAGAAAGCCAAGGCTTCACAGAACAGCACTTTGAACGAATCAAAAGTCCTGAGGTTACAGAGATACAAATTGCCAAAGAGCACCCATCGCAAGTAATGTCTGCCTTAACTGAGAGTGTAACTCCATTAACGATTGTCAAAGCAGAGCCATTATCCACTTTAGAAACAGAAAAGATTAAGGCATCTCCTGAGCCCAAGTATCCAATATCAAGTCACCAAGTTGAGACAAAGCTCCCAATTGTTAAAGAACATTCAGAGGTTATACCCCATACTCAGCAAGAAAAGGGTTATCAAGTTAAAGAGGGAGTTAAAATTCTTTACAGTGCAGTTTCATCAGAGAAACAACAGTTTACAGAGGGTCACTCTAAAGAACTATCAACAGAAGAACCAACTTTTCAGACATCGGTGAAAAAAGAA[C/T]AACACAAACCGGTTGTACTTTCAGTTAATGAGACAACTCAGACCTTATCTAAGGAAGAGAGCTTATCAGTGCAGAAACCAGGTGTTGAGACTGCATCTCAAGTGAAAGACAGTGTCTTTAAATCAGCTCTTGTTGCTGAGGAAAAGCATCAGCTCCAAGCTGATCAGTCAAGTTTGATTCCAGGTTTAGACAGTGCAATTTCAGTGCAACCCCTAAGAGAAGAAGAACAAGTTCAACATTTGCAAGTTATCACAGATCAAGGTATTCTTCCAGCTGAAGGAAGGTTTAGCAGTGAGAACCCAAGCCCAGAGAAAGCAGATGCTCAAAAAAGTCCTCTACTTAAGCATACAGTGTCAGTGGATTTACAGCAGACAGTGACATGTGAGGAGTCCTCAGAGTTTTCAGGACAAGTAACAGAGCTTTCTATTCAGCCTGGTAAGGCAGCGCCTGCCCCTTTGCATCTTCAGGCAGTTCATTCAGAAAATTTGTTGACGAAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34746
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 3803 | 7601 | 34 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 3803 | 7601 | 35 | 75 |
ENSDART00000109099 | Nonsense | 4326 | 31319 | 43 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44103045)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43228215 |
GRCz11 | 9 | 43030002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCATGAGGTAAAAGTAAGGAAAGAACCCAAATATCTCATGTTCACTTA[T/A]CTTATTACAAGTGCAAGTGCTCCACTTGAAATTACAATTGCATTTGAAGG
Long Flanking Sequence:
TCAATTGAGAAATTTGTATCTAATATCAAAGTTGAACCAAAAATACCATCTGAATTAATTTATGTAGAAGAAAAGGCTATCTCAACAGAGAGTAGCATTGCCCTTGAGGCCACCGAACAAGACTTTGCACTTCAAATTCAGGAAGGTCAGTCTGTTAGGCAGTCAGTGTTAATGGAGGAAAAACGTGTTATTAAAGGTGAGCTTTCTCAGGATATTACAAAGTCTGAAACAACCACAGCAGTTGTCAGTGAGCAGAAAATGGGTACGCTTTTAGTGTCAGAGTCAAGAGAGAGCCAGAGTTTACCCAAGGAGCTCACTTTTGTCGTTTCTCCCCCTAAATCACATTCACTAGACATTAAGCACCAGTTAAAAAGTACACTTGCAACTGCAGTCGCTCTTGACCAGCCATTGATCCTGGCCGATTTTGTGGAGAGTTTGGGAGTTGTAGAAATTCATGAGGTAAAAGTAAGGAAAGAACCCAAATATCTCATGTTCACTTA[T/A]CTTATTACAAGTGCAAGTGCTCCACTTGAAATTACAATTGCATTTGAAGGCGAGTATCCTCAGACTGCTGATCTCAGAAGTGAACTTCAAGCTGCTTTTTACTCTATTGTCTATCGAGAGCAGAACGTTCTGACCTCAGAGCAGCCAGGCACATTACAAATTGATAGACCCCAAAGACTACAGGTCACAAAGGCTTCTACAAAAGAAATGCTTTCACCTGTGGTGGAAATGGTTAGGCTCTCAGAAAATGTGGAGCCTTTCACATCTCCAACGTCTCAGTCAGCAACTGTGAAAACTGAAGCCAAAACATCTTTTCAATCTGTGACTGCTAAAGAGCAAGCTTTTGTGCAAGAGTCAATTCATATAGCAAGTGAATCAAAAATTGAGATTCAACAGTCCATTCAAGTTGAGCAACAGGAAACCAGATCTGTGACAGTAAAAAGTGCTACAAGTATGACAAGTGAGCTTGTTTTAGGACCTCTTCCAATTGAACGGTCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31747
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Essential Splice Site | 4090 | 7601 | 34 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Essential Splice Site | 4090 | 7601 | 35 | 75 |
ENSDART00000109099 | Essential Splice Site | 4613 | 31319 | 43 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44102184)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43227354 |
GRCz11 | 9 | 43029141 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGCTGGCAAGACCTCTACATCGTCCCACCTCACTGTGATCCCAAGAGG[T/C]TGGAATTATGGGAATATTTTGTCATCCCATCCCACATGACTAACTCTGTT
Long Flanking Sequence:
CATATAGCAAGTGAATCAAAAATTGAGATTCAACAGTCCATTCAAGTTGAGCAACAGGAAACCAGATCTGTGACAGTAAAAAGTGCTACAAGTATGACAAGTGAGCTTGTTTTAGGACCTCTTCCAATTGAACGGTCCACTGAAATTGCCTTTCAGAAAGAGGAAAAGGAGGAATACATAACTGAAGCATTAATGGAATTAGAGAAAGAAGATAAAGAGGGATACCCAGTTTTTGAAAACTCTTTGGAGGATATTAAAACAGAGGAGCATTCAGAAGCTAAGTTTTCATTGATTATCCGATACGTAAAGAAAGTAAATTGGCTCTTTAATGGAAAATGTATTAAATCTGGCAAAGAGTTCAAGTGTTCTAAAGAACATGACACTTACACACTAGTAATCACCAAGGTAATGAAGGATCATGAAGGAGAATATACCTGTGAGGCTGTAGGTGAAGCTGGCAAGACCTCTACATCGTCCCACCTCACTGTGATCCCAAGAGG[T/C]TGGAATTATGGGAATATTTTGTCATCCCATCCCACATGACTAACTCTGTTCATAGCTAAAATAGAAATGCTTCATTAGACACGCATTCTCAAGATCTCCACAAATATCAGCAGTGTTGGGTAAAGTTACTTTTAAAATAAATATACTGCAACACAGTCTTAAGCCTTAATCTTTATGAAGTCTTAATCTTTAAGAAAAACATGATGTACGTGCACATTATCTAAAAGTAAATCATTTAATTATTTAAAAATTTTAAAAAATTATGACTAAAGATTGTATTATAAAGTAACTTTTCTCATCACTGTCTATCATTTGAATATATCTTCATGTTTTTCTCTTTGTGAATTTTGTCACCATTTTCACATTTCTGAAATGTTAGCATGTCTTCACATTCTTTACACCAACTCTTAACCTGCTGGATTATTCAGTTTCATTTCAACATTTGTCATCTTATTCACTCTTGCAGAGTTTCACTTTTCATTTTGTTCATCACTGAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14817
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 4203 | 7601 | 36 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 4203 | 7601 | 37 | 75 |
ENSDART00000109099 | Nonsense | 4726 | 31319 | 45 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44100795)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43225965 |
GRCz11 | 9 | 43027752 |
KASP Assay ID:
2260-2414.1 (used for ordering genotyping assays)
KASP Sequence:
CACCAGAATTTGTAWCAAAGCCTGATTCGATGACTTTATTTGTTGGCAAG[C/T]AGGCAAAATTTCAATGTGTTATTTCTGGTTCTGAGCCAATGAATGTTGTC
Long Flanking Sequence:
TATTTTTTTTATCTGTGTGCACTATTCAGTGCCACCCGTTTTTAGGCAGAGAATTCAGAATCTGGAGGTGAATGTTGGCAGTTCTGCAAAGTTCGAATGTGAGATTGAGGAGGCTCCTGGTGTGACCTTCAAGTGGTTCAAATCGGGTACTGAGCTCAGGCACAGTGAAAAATGCAGAATTATAAGCCGACACCACACATCATCGCTGGAGATCTTTAGCCCAGCAGTCGCTGACAGTGGAGAATATACCTGCAAAGCTTCTAACCGCCATGGAAGTGATAGCTGCTCTGCTAAACTAACTGTGACAGGTAAGAAAAATATACATTTCTTATTGGCTGTTGGACTTCTTGAAATATTCAAATCTGGGGTTGATCTGATTTTTGTGTGATACTCTTTTGACTAAGTTATTGATATCTTCTTACTGGTATGTTCTTTTTGTAGAGCTTTTCCCACCAGAATTTGTATCAAAGCCTGATTCGATGACTTTATTTGTTGGCAAG[C/T]AGGCAAAATTTCAATGTGTTATTTCTGGTTCTGAGCCAATGAATGTTGTCTGGCATAAAGACAATATTGCCATTTCACTTGATGACCACTACAAAGAGTCTTCTGACAAGAACCGGTATTTTCTTGAAATTTTGAATCTACAGCACAGTGATCAAGGCACATACCTTTGCAAAGCTTCCAATAGTGTTGGTACAGCAACATGCTGCACTGAACTGAGGGTTGTAGATAAACCCAGCTTTGTGAAGAGCTTTGAGTCTACCACTGTTGCTGTGGGAAACCCACTACGTCTTGAGTGTCAGGTAGATGAGGACACTGGTGTTTCCATCATTTGGATGAGAGATGGCAAGAAACTCCATACTACAATGGATTGTAAACTAGCATTTGAGGAGAAAATAGCCTGTCTTGATATTCAGAAGTCCAAACTCAAAGATACAGGCACATATACCTGCACTGCTGCCAATGAAGCAGGAAGCAGCAGTTGCTCTTCTAGTGTGACAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30647
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Essential Splice Site | 4651 | 7601 | 39 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Essential Splice Site | 4651 | 7601 | 40 | 75 |
ENSDART00000109099 | Essential Splice Site | 5174 | 31319 | 48 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44099004)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43224174 |
GRCz11 | 9 | 43025961 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAAATGAGGCTGGAAAACAAAAATGTGAGGCCACTGTAACAGTTCAAG[G/A]TTAGAATTTTAATACTGTTTTATTATGAAATACTTTATCATTATTATTCT
Long Flanking Sequence:
CAAAGGAGACAGCAGCCTATTTGGAAATCAAAACATTTGAAAGTGCAGATGTTGGAGATTACCAGTGCTGCATTTCCAATGATGTTGGTAAAATAACTACAAAAGCGGTGGCCAAACTGAAAGGTTAGTACAGTCAGTGATTACTAAACAAATCATTTAGCTGTTGCTGTCACTATTTTATTTAATGTGAAAATGAATATGCATTTTTTTTCATGCAGACCCACCATCCTTTGTAAAGAAAGTTGAGAACACTACTGCGGTTTTAGGCAGTGCTGTAAAACTGCAAGGGACTATTAAGGGTTCTGCTCCTATCACAGTTCAGTGGTTTAAAGATACAGAGATAGTCAGAGATGATGATCCTAATATCACCACAACCTTTGAAAACATCATTGCTGTTTTAGCTATTTCCAATGTGGCCATTAACCATGGTGGGAAATATACTTGTCAAGCTGAAAATGAGGCTGGAAAACAAAAATGTGAGGCCACTGTAACAGTTCAAG[G/A]TTAGAATTTTAATACTGTTTTATTATGAAATACTTTATCATTATTATTCTTCACTGTTATCTGATTGGCATATTAATGATTTTCATTTTTTTAAAGAACCAGCTAGATTTGTTGAGAAACCCCCATGCATCAGTGTGACTGCAGGTGACTCTGCAACTCTTGAGTGCAAGGTTTCAGGAAGTCCAGATCTCAAAGTTAAATGGTTTAAAGATGGCAAAGAGATGGCAGGGGGTCGAAAGTACAAAATCACTTTCAAAGAGAATGTGGCCGTCTTGAAAATCCTCTCGGCAGAGAGAGGAGATAGCAGTGAATACAAAGTTGAAGTATCCAATCGAGTTGGAAAAGAGCAGTGTTCTTGCTCAATCAATGTTCTTGGTTAGTGCTATTTTTTGAATTGCCTTGACTTTTTTGTGTGTGTCTGTGCATTTTTCTAACAAGAGTGTTTTACTGTTTTGAGCAGATAAAATAATACCTCCAACTTTCACAAAAATGCTTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21581
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 4700 | 7601 | 40 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 4700 | 7601 | 41 | 75 |
ENSDART00000109099 | Nonsense | 5223 | 31319 | 49 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44098762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43223932 |
GRCz11 | 9 | 43025719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGTTAAATGGTTTAAAGATGGCAAAGAGATGGCAGGGGGTCGAAAGTA[C/A]AAAATCACTTTCAAAGAGAATGTGGCCGTCTTGAAAATCCTCTCGGCAGA
Long Flanking Sequence:
TTGAGAACACTACTGCGGTTTTAGGCAGTGCTGTAAAACTGCAAGGGACTATTAAGGGTTCTGCTCCTATCACAGTTCAGTGGTTTAAAGATACAGAGATAGTCAGAGATGATGATCCTAATATCACCACAACCTTTGAAAACATCATTGCTGTTTTAGCTATTTCCAATGTGGCCATTAACCATGGTGGGAAATATACTTGTCAAGCTGAAAATGAGGCTGGAAAACAAAAATGTGAGGCCACTGTAACAGTTCAAGGTTAGAATTTTAATACTGTTTTATTATGAAATACTTTATCATTATTATTCTTCACTGTTATCTGATTGGCATATTAATGATTTTCATTTTTTTAAAGAACCAGCTAGATTTGTTGAGAAACCCCCATGCATCAGTGTGACTGCAGGTGACTCTGCAACTCTTGAGTGCAAGGTTTCAGGAAGTCCAGATCTCAAAGTTAAATGGTTTAAAGATGGCAAAGAGATGGCAGGGGGTCGAAAGTA[C/A]AAAATCACTTTCAAAGAGAATGTGGCCGTCTTGAAAATCCTCTCGGCAGAGAGAGGAGATAGCAGTGAATACAAAGTTGAAGTATCCAATCGAGTTGGAAAAGAGCAGTGTTCTTGCTCAATCAATGTTCTTGGTTAGTGCTATTTTTTGAATTGCCTTGACTTTTTTGTGTGTGTCTGTGCATTTTTCTAACAAGAGTGTTTTACTGTTTTGAGCAGATAAAATAATACCTCCAACTTTCACAAAAATGCTTAAAAAGGTAGACGGTAATGTTGGAGCTAGTATTCAAATGGAGTGCAAAGTGTCAGGATCCCAGCCCATAACAATATCTTGGTTCAAAGAGGGAAAGGACATTACAACTGGAACAAAATATCAAACTGAAATGCAGGAAAGCACTGCCTTACTCAAAATAACAAATTTAGAGACATCAGATGCTGGGGTTTTCACATGCCATGCAACTAATGCTGCAGGACACAGTGAAACAAGTGGAACTATTTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21580
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Essential Splice Site | 6071 | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Essential Splice Site | 6071 | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 6559 | 31319 | None | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44092358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43217528 |
GRCz11 | 9 | 43019315 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAATGATGCTGGGACTAAGAGTTGTAGTACAGCTCTCACAATCAAAGG[T/C]TAGATAGTGGAAGAACATTTTATTTACTAGTTTATTATGAGCATTGTCTG
Long Flanking Sequence:
GCTTTACCATCTGCATGTTCTTATTTCGCTTGTGAACATTGTGCATATATACTGTACCTTACATCATCATCTTTCACCATTGCTGCTCATTACGCTTTACTCCCTTTCAGCTATCATCTTCCTCTTGCTATCTTCCATCTTCTTGAAATCATCATCAGCGCTCTATTTTATACATTGCAATAATCATTTCTAACATGTTGTAATTTTGGTTTTACAGAACCTCCAGAGTTTGTACAGAAACTGCCAGCTGCAAAAGTCGTAAAAATGGGGGAGCCGCTGCAGCTTGAATGCAAAGTTACTGGGACAGCTCCTCTGAGAATAAGCTGGTACAAAAACGATGCCATACTCAGTGATGGTGGCAACTTGAGAATGACTTTCGATAACTCTGTGGCAGTCCTCGAAATTTCCACATCAAGCTTTGATGATAATGGTGTCTATACATGTGAAGCACAGAATGATGCTGGGACTAAGAGTTGTAGTACAGCTCTCACAATCAAAGG[T/C]TAGATAGTGGAAGAACATTTTATTTACTAGTTTATTATGAGCATTGTCTGACAGGAATTGTGTTTCAATAAATAAAATAAAAAAATTAAATTAATTAAAAAAGTTTTTAATAATTAAGAGTAGATTTCATTGTCAATTGTTTTCATTATACACTTATATTTTGTGTGTGTATATATTTAGTATTAGTCTTATTTTATACATAAATAATTACAAATTTATTTATTTATTTAGTTTTCAAGAAAATGTTTTAAAATTTAAAGTTATTTAATATTTAATTTTATTATTCTATTTTGTTTTCATTTATTTTAACTAGATTAATTGAGAAGATAGTTCATACATAATCCCTGGTCTTTTTGTTTCAATTAGCATATGTTCTCCTGTTATGTTTTTGTAGAACCACCAAGTTTCTACAAACTGCCAACACCAGTTGAGGGGCTGAAAGGCAAAGATGCCAGTCTTAACTGTGAGCTGAAAGGCTCTGCACCATTTGAGATAACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16898
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 6143 | 7601 | 56 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 6143 | 7601 | 57 | 75 |
ENSDART00000109099 | Nonsense | 6631 | 31319 | 64 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44091746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43216916 |
GRCz11 | 9 | 43018703 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGCAACTCTCCACATTCTCGGACTGGAAGCATCAGATGCTGGAGAATA[T/G]GAGTGCAAARCAACAAATAATGTTGGAAGTGATTTGTGCCAAGGCTCTGT
Long Flanking Sequence:
AATTAAGAGTAGATTTCATTGTCAATTGTTTTCATTATACACTTATATTTTGTGTGTGTATATATTTAGTATTAGTCTTATTTTATACATAAATAATTACAAATTTATTTATTTATTTAGTTTTCAAGAAAATGTTTTAAAATTTAAAGTTATTTAATATTTAATTTTATTATTCTATTTTGTTTTCATTTATTTTAACTAGATTAATTGAGAAGATAGTTCATACATAATCCCTGGTCTTTTTGTTTCAATTAGCATATGTTCTCCTGTTATGTTTTTGTAGAACCACCAAGTTTCTACAAACTGCCAACACCAGTTGAGGGGCTGAAAGGCAAAGATGCCAGTCTTAACTGTGAGCTGAAAGGCTCTGCACCATTTGAGATAACATGGTTTAAAGATAAAAAACAGTTAAAGGAGAGCAGGAAGTATAAATTTGTTTCTGAGGGATGTTCAGCAACTCTCCACATTCTCGGACTGGAAGCATCAGATGCTGGAGAATA[T/G]GAGTGCAAAGCAACAAATAATGTTGGAAGTGATTTGTGCCAAGGCTCTGTAAAGCTACGAGGTCAGTAAGATAGCAGTTCAAAGTATGGAATAATTTTCCAACAAATTTTTTTCATATTAGTTTAACCATTCTCTTCCTAAAATTCAGAACCACCTGCATTTGTGAAGAAATTATCCAATACGACAGCCATCTCTGGTGAGGAGGTAGTTTTGCTGACAACAGTCAAAGGCTCTCAGCCTATGACTGTATCTTGGGTTCAGGATAAAGACCACATACTCAGAGATGGTGAAAACAGAAAAATTACATTTGAGAATAATGAGGTCACCTTGAAGGTCTTTAAAGCTGATTCTACTACTGCTGGAAAGTATACATGTCAGCTAAAAAATGATGCTGGAGTAGCTGAATGCACAGCGAACCTAACTGTCTTAGGTACTTGTAAAAATATATATGCTTTTCACACAAATATATTTCATGTTTATTATGTTTTTTAATTAAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15104
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Essential Splice Site | 6164 | 7601 | 56 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Essential Splice Site | 6164 | 7601 | 57 | 75 |
ENSDART00000109099 | Essential Splice Site | 6652 | 31319 | 64 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44091683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43216853 |
GRCz11 | 9 | 43018640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAAATAATGTTGGAAGTGATTTGTGCCAAGGCTCTGTAAAGCTACGAGG[T/C]CAGTAAGATAGCAGTTCAAASTATGGAAWAATTTTCCAACAAWTTTTTTT
Long Flanking Sequence:
ATTTAGTATTAGTCTTATTTTATACATAAATAATTACAAATTTATTTATTTATTTAGTTTTCAAGAAAATGTTTTAAAATTTAAAGTTATTTAATATTTAATTTTATTATTCTATTTTGTTTTCATTTATTTTAACTAGATTAATTGAGAAGATAGTTCATACATAATCCCTGGTCTTTTTGTTTCAATTAGCATATGTTCTCCTGTTATGTTTTTGTAGAACCACCAAGTTTCTACAAACTGCCAACACCAGTTGAGGGGCTGAAAGGCAAAGATGCCAGTCTTAACTGTGAGCTGAAAGGCTCTGCACCATTTGAGATAACATGGTTTAAAGATAAAAAACAGTTAAAGGAGAGCAGGAAGTATAAATTTGTTTCTGAGGGATGTTCAGCAACTCTCCACATTCTCGGACTGGAAGCATCAGATGCTGGAGAATATGAGTGCAAAGCAACAAATAATGTTGGAAGTGATTTGTGCCAAGGCTCTGTAAAGCTACGAGG[T/C]CAGTAAGATAGCAGTTCAAAGTATGGAATAATTTTCCAACAAATTTTTTTCATATTAGTTTAACCATTCTCTTCCTAAAATTCAGAACCACCTGCATTTGTGAAGAAATTATCCAATACGACAGCCATCTCTGGTGAGGAGGTAGTTTTGCTGACAACAGTCAAAGGCTCTCAGCCTATGACTGTATCTTGGGTTCAGGATAAAGACCACATACTCAGAGATGGTGAAAACAGAAAAATTACATTTGAGAATAATGAGGTCACCTTGAAGGTCTTTAAAGCTGATTCTACTACTGCTGGAAAGTATACATGTCAGCTAAAAAATGATGCTGGAGTAGCTGAATGCACAGCGAACCTAACTGTCTTAGGTACTTGTAAAAATATATATGCTTTTCACACAAATATATTTCATGTTTATTATGTTTTTTAATTAAATGACTCTTCTAAATTTTTAGAACCTGCAGCAATTGTGGATAAGACAGATTCAATCAGTGTAACTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8690
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 6360 | 7601 | 59 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 6360 | 7601 | 60 | 75 |
ENSDART00000109099 | Nonsense | 6848 | 31319 | 67 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44090829)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43215999 |
GRCz11 | 9 | 43017786 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTATTCTGTTTTTTGTCGAACAGACAAAATTGTCCCKCCTTTGTTCWCA[C/T]GAAAATTGAAAGATACRCAGAGTATTGTTGGAAAATCTATGGAATTGGAC
Long Flanking Sequence:
CCTAACTGTCTTAGGTACTTGTAAAAATATATATGCTTTTCACACAAATATATTTCATGTTTATTATGTTTTTTAATTAAATGACTCTTCTAAATTTTTAGAACCTGCAGCAATTGTGGATAAGACAGATTCAATCAGTGTAACTGCTGGTGAAGCCGCAGCCTTAGAATGCACTGTATCTGGAACTCCAGAACTTAAACCAAAATGGTTTAAGGATGGTGTGGAGCTGTCTTCAGGGAAAAAATACAAAATTACCTTTTCAAAGATGATTTCCAGTCTTAAGTTATTGTCAACAGAGAGGAGTGATACTGGAGAATACACTTTCAGTATCAAGAATGAAGTTGGCAGTGACAGCTGTGCAATGCAGCTAACTGTTTTGGGTCAGTAATTTTTTATAAGGTTTCTTACGTTCTTTAAACTGCATGTAATTTCTTATGAAGCTATACATTAAGTATTCTGTTTTTTGTCGAACAGACAAAATTGTCCCGCCTTTGTTCTCA[C/T]GAAAATTGAAAGATACGCAGAGTATTGTTGGAAAATCTATGGAATTGGACTGTAAAGCTTCGGGGTCTGCACCTCTCACAATCTCTTGGTTTCACAATGAAGTGGAGATCATGAGTGGACCAAATTATGAGATTACTTTCACTGAAAATACCTGCACCCTGAAAGTGCCTACTCTGAAGCTTTCAGACTCGGGTACATACAAATGTAAAGCAGTGAACAGTGCAGGAGCAGCAGAGACATCTGCTTCCTTAGTTGTTAAAGGTTAGTGTTTTGCTGTAATTTGAAATAAGTTAGAAGTATAAATATGTTAGTTAAATCACCTATTACACCCCTTTCCCTGTCGTATTTGCTATAGAACCACCCTCTTTTGTGACAACACCTCAACCAGTGGAAGCCCTTCCAGGCACAACTGTTACTTTTACAGCAACTGTTCAAGGAAGTACCCCAATGAAACTGAAATGGTTTAGAGGCAGTAAGGAAATAGTGTCTGGAAGAAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41538
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 6499 | 7601 | 60 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 6499 | 7601 | 61 | 75 |
ENSDART00000109099 | Nonsense | 6987 | 31319 | 68 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44090317)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43215487 |
GRCz11 | 9 | 43017274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTAGAGGCAGTAAGGAAATAGTGTCTGGAAGAAGCTGTGAGATTGCGT[T/A]AAGAGGAGATACTGCAATTCTGGAGCTCCACAACATTGACAAATCTCATG
Long Flanking Sequence:
GATACGCAGAGTATTGTTGGAAAATCTATGGAATTGGACTGTAAAGCTTCGGGGTCTGCACCTCTCACAATCTCTTGGTTTCACAATGAAGTGGAGATCATGAGTGGACCAAATTATGAGATTACTTTCACTGAAAATACCTGCACCCTGAAAGTGCCTACTCTGAAGCTTTCAGACTCGGGTACATACAAATGTAAAGCAGTGAACAGTGCAGGAGCAGCAGAGACATCTGCTTCCTTAGTTGTTAAAGGTTAGTGTTTTGCTGTAATTTGAAATAAGTTAGAAGTATAAATATGTTAGTTAAATCACCTATTACACCCCTTTCCCTGTCGTATTTGCTATAGAACCACCCTCTTTTGTGACAACACCTCAACCAGTGGAAGCCCTTCCAGGCACAACTGTTACTTTTACAGCAACTGTTCAAGGAAGTACCCCAATGAAACTGAAATGGTTTAGAGGCAGTAAGGAAATAGTGTCTGGAAGAAGCTGTGAGATTGCGT[T/A]AAGAGGAGATACTGCAATTCTGGAGCTCCACAACATTGACAAATCTCATGCTGGCGAGTACACTTGCCAGATCATTAATGATGCAGGGAAAGAAAACTGCCCTGTGAATCTTTTTGTTAAAGGTTAGTTTTAATTTGTTAATACTATAGAGGCTTAAAGGTTTCTTCATTGCTTGATATAGCAGAACTTTGTGTCTTACATCTTCATACATGCCATCCTTCATTCAGAGGCTGCACACTTTGTCAAGAAGCTAAAGAACCTCTCAGTTGAAATGGGCAAGTCACTGATACTTGAATGCACATATGCGGGGAGCCCAAAGATTCTTGTGAAATGGCATAAAGATGGCCAGGAGATTTACTCTTCATACAAGTACAACATTACGACCACTGAGAGCTCCTGCATACTAGAATGTCTAAACAGCGATAAAGAGGCTGCTGGGAAATACACTTGTGAGGTTTCCAATGATGCTGGACACGACATTTGTGAAGCAGCAGTGTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21579
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | Nonsense | 7472 | 7601 | 72 | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | Nonsense | 7472 | 7601 | 73 | 75 |
ENSDART00000109099 | Nonsense | 7949 | 31319 | 80 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44080563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43205733 |
GRCz11 | 9 | 43007520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAAGCTTTTAGAGCCTCACAGCAGATATACATGTGCTGTGGCCAATTA[C/A]ACTCAGAAGCTCTCAATCAAAGATGTTAGGCCAGAAGATCAAGGAGAGTA
Long Flanking Sequence:
ACAGACCAGACAACTACTGTTAAGAAGGAAGCTGTGTTTGAATGTGAGATCAAGATTAACTACCCCGAAATCACTCTGTCCTGGTATAAAGGAACACAAAAACTTGACAGTGGCGACAAGTATGACATCAAAATTGTGGGTGATCGTCACATTTTAAAAATCAAGGACTGCCAGACAAGAGATGAGGGAAATTACCGTATTGTGTGTGGCCCACATATCTCCAGTGCCAAACTGACAGTGTTGGGTATGTAGAAACATTTTTTGAGGTTTATTTTAGTGAATATGCCTCATGCTATATCAAATATGCGTTTTAAAATAACAACCTTTATTCTTTCTGCAGAAGCTGAGGTGGAAAAGCCTATGCAGGATGTGGCTGGTAAGGAAGGCCAGACATGTACATTGACTTGCCAGTTGTCTGTACCTAATGTAAAAACCCAGTGGTTTAGAAATGGGAAGCTTTTAGAGCCTCACAGCAGATATACATGTGCTGTGGCCAATTA[C/A]ACTCAGAAGCTCTCAATCAAAGATGTTAGGCCAGAAGATCAAGGAGAGTATACCTGCAAATATAAAAATCTTGAAACGACTGCCAATCTTTGGATCGAAGGTTGGTATAGATTAACTGAACTGTCAGATTGTAAAATAGACCATCTACTAACCTCTTCTATCATCATCATCATCTGTGACTTCTTCTTAACCTCTTCTTAACCACACTCTTCTTGTTTTAAATGCCAGGAATGTTTTGTCTTCATATTTTCCTGGCTTTCTTTTATCGCAAAACATAAGAGAGTATGTTAGGCAAATACAAATAGATTCCGCTCCTAATCATCCACCTTGCGTTATTCCTTTCTAGCTGAGCAAATACATTTCACCAAACGCATCCAGAACATTGTGGTGAGAGAACATCAGTCCGCCACTTTTGAGTGTGAGGTGTCTTTCGACAATGCAGTTGTAACATGGTATAAGGACACTTGGGAGCTTAAAGAGAGCCCCAAATATACATTCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12471
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 8734 | 31319 | 93 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44071747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43196917 |
GRCz11 | 9 | 42998704 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCACCTTCTCCTAAAAAGGATGACATAGTACCTCAAAAGATTCCTAAA[C/T]AAGATATATCTCAGACTAAGCCTCATATGAAAGAGATGATTCCCACACAA
Long Flanking Sequence:
TTCCTGCTAAACAGAAAGATAAAATTGTTCCTCAAAAGAAAGAGGTCACTCCTCTTTCTAAAAAGGATGAGGCAACTGCACCTAAAAAGACAGAAATGCTTCCTCCTGCTAAACAGGATGAGGAAATTTTTCCTCAAAAGAAAGAAGTTGCTCTTCCTTCTAAAAAGGATGAAGCAGTTGAATCTAAAAAGAAAGATGTTTATTTTTCTGCTAAACAGGATGAGGAAATAATACCTAAAAAGACAGAGGTTCTTCTTCCTCCTAAAAAGGAGGAGGCAATTGAACATAAAAAGAAAGACGTTTCTTATCCTCGTAGAAAGGATGAAGAGCATGAACCTATAAAGAAAGAGGGTCCTCTTCCTTCAAATAAGGAGGAAATTGTAAATCAAAAGAAAGATGTTCCTTTTCCCACTAAACAGAGCGATGAACTGTTGCTTAGAAAGAAAGATGTTCCACCTTCTCCTAAAAAGGATGACATAGTACCTCAAAAGATTCCTAAA[C/T]AAGATATATCTCAGACTAAGCCTCATATGAAAGAGATGATTCCCACACAAATTCCAGAGAAGACAGAAGAAAAAGAAACTTTCTCCGTACAAGTAGTTACACGTCTACAGAAGGAAGTGGTACTTGCTGCAGAAATTCTTTCAGAAAAAGAAGAAACGGAAGAAATTTTCCTTAAAGAAGAAATTAAACATCTTCAAAAGGAAGCTTCTCTTAAACCAAAGCTGGAAGAAAAAGAAGATATATTGCCTAAAAAGAAGGAAGTAATTGCCATGACTAAAAAAGAGGAGGTCATAATGCCCAAAAAGAAAGAAATTCCTCTTCTTGCTAAAAAGGATGAAGTACCCCAAAAGAAAGAGGTGACCCCTACAAAAGGTACAAAGATATCTGACAACATCTTAGTCTTTTTTATTCCTTGTCTTTATGTTTTAGAAACTCTCTTGAACTTATCTTTAGCTATTTCATTGTACTAATTTCTTTGTGTCTGTTGAGTCACGTATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41537
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 8989 | 31319 | 95 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44070263)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43195433 |
GRCz11 | 9 | 42997220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTACAGAGGGAAATTTAATCAAGAAAGATAGAGATGGAAAATTACCT[C/T]AAAAAAGAGTGACAGATGCTTTCCCCAAAAAAGAAGAAATGACAGAGATA
Long Flanking Sequence:
CCAAAATCTTCAAGATGTCACTTCTGCTCTAAAGAATGATGACGCCATTCAGTCAGACAGTCAAGGAATTGCAGTGAAGCCACTTCTTTTGGAAGAAACCCATAAAGAGGACACCTCTCATTTAGAACTTGTATCACAAACAGAAATACTCCATGGAGCAATAGGTAGCAAAGAGACTGAGAATTTACATATTACAAAACTGGAGGATTCATCAAAAGAAAGTATATTTTCTTCAGAATTTACAAATGAATCATTTTCTCATGAAGGGCTCCCTAGAGAACTTGTAATGACAGGTAAGCTAAACAGTGCTCACAAAAGGATTTTGAAATTGTGGATTGAGAGTTTTGTTTAGCTGCACCTCAAGAGACAATGTTATTTTGCCTTCAGCCTATGAAAAAAATTCCTTTGAATTCCAAGAATCTTCCATGAATCCAGAGGTTGCTCTGTTTATTGCTACAGAGGGAAATTTAATCAAGAAAGATAGAGATGGAAAATTACCT[C/T]AAAAAAGAGTGACAGATGCTTTCCCCAAAAAAGAAGAAATGACAGAGATACTTTCTAAAAAAGAGACATTTACTGACCCTAAAACGAAGGAAATTGTGCTTCAAAATGAAGAACGTCTTCAAAAGAGATTTCAAAGCAAACCATTTGCTGATTCTCCCCAAAAGAATGAAGACATTGCTGTAATAGAATTTTCCCAAAGAAAGAATGAAATATTAACTCCTAAAATGAAAGCAGTTCCTCTTCCTCCTAAAAATGAAAAGGCACTTCAAAACAAACATATTTCTCATGATGCTAAACAGAGTGAGGAAATGTTACCCAAAGAGATTGATGATTGGTCTAGAAAAGCTGAGGAAATGTCATGTGAAAAGAAAATTGCACTTCCAAAGAAACGGGTTACTCTTCTTCCTAAACAGGATGATGAAGTGTTACATAAAGAGAAAGATGTTCCTTATCCCCCTAAAAATATTTATCTTCCCTATCAAGAGGAAGATGAAATTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34745
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 9897 | 31319 | 95 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44067539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43192709 |
GRCz11 | 9 | 42994496 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAAGGTCCTCTTTTTAATAAAAAAATAATAGAAAATGCATTTAAAAAC[A/T]AAGATGTTCCTCTTCCCATTAAACAGGGATTGACCCCTAAAAGGGAAGAT
Long Flanking Sequence:
TTAAACAGGATAAGAAAATGCTACTTAATGAAAAAGATCATCCCATAAAGGGTGATGAAATTTTATTAGAAAAAAATGAGATTTCTCCCAGAATGGAAGATGACAAGTCTAAAGCAAAAGATGTTCTTTCTAAAAAAGAAAAGGAAATTGCCTATAAAAAGAAAGAGGCTTCTCTTTCTGCTGATAAGGATCAAGAAATGTTTCCTAAAAAGAAAGAAATTTCTACCAACCAGGATGAGAAAATATGGGATCAAGAGAAAGAGGTTCCTTTTCCCTCTAAAACGGAAGGTGAAACTGTATCTGAAAAGAAAAAGGTGTATCTTCCCTCTGAAAAGGAAGATGAATGTTTGCTTCAAAAGAAAGAGGTTCATCTTCCTGTTATACAGGATGACAGCATGTTACAGAAAGAAATGTTTCACAGAAAAGAGGATGAAATTGTATCTAAAAAGAAAGAAGGTCCTCTTTTTAATAAAAAAATAATAGAAAATGCATTTAAAAAC[A/T]AAGATGTTCCTCTTCCCATTAAACAGGGATTGACCCCTAAAAGGGAAGATGAAGTAACTGTGTTTGACAAGAAAGAAATGGGTTCTCTTCTCAAAATGGATAAAGGAATTTTACCTAAACTGAAACCAGTTTCTTTTCCTCATGAGGATGAAATATCTGTCAGTCAAAAGAAAGACATTCCTCTTCTTTCTAATATGGATGAAGAAACAGTAACTCAGACTGAAGATATGACTTCCACACCAACAGCAGAAGTTGTAGTTCTACTGAAAACTAAGCAGGCTTCTCAAACAAAAGAAACTGTTCGTCAGAAGAAAGAAATAACCCCCACACATATTTTGAAAGAAAAAGAAGAAAGTGCTCCTAAAAGAACTGGTTATCTCTCTTCCGATTGGGAAGAAATTGCACATCAACATAAGGAAGTGCCCCTAACAATAAAACTGGAAGATAAAGACAATAAGCCAAATAAGGCTGTTGCATTTGCTAAACCAGAGCACCTTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17286
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | None | 10183 | 31319 | 97 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | Essential Splice Site | 225 | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44065400)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43190570 |
GRCz11 | 9 | 42992357 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATAAACTCATCTCAAARCCCAAGGAAGAGAAGACAATTCCAACAAAAGG[T/A]ATTATGTTARCCTCAAGTCTGCACCCCTGTAAGTTCCTGAAAAGGAARGG
Long Flanking Sequence:
ATCTTTAAAGCACTTAAAAGTTGCTGAAACATGCTCCAAATTTATATGAATGCATGTTTGCATGAATGAGAATGGTCTAATTTTTCAACTACTTCAACTACTTGACATACCTCCACACTTCCTTTTGACCAGACCTTGATGTCCACTTGTATTTATCTTATAGCAGTGTTTAATCTGTAAATAAGTTCTAATCTACAGTTTGGTATCTTATTCTGCCGCATAAAGGTTTTTTACTAAAATGACTGATTCTTTCTATTGATTTGCACATATATAGAGTAGATTTGAGCAGAGCATTTCATGTATGTTATGCATGTAATAACTCTTTGTCAGTTTCTTAGCCTCGATAGAGGTTTGAAATACTTTATTCTTTCATCACTTTTTATCTTAAACATCTTTCAACATCCAACAAAACTCTTTTTTGAAGTTAAAGAGGTCGATAAGAAAGCTGAAGATAAACTCATCTCAAAACCCAAGGAAGAGAAGACAATTCCAACAAAAGG[T/A]ATTATGTTAACCTCAAGTCTGCACCCCTGTAAGTTCCTGAAAAGGAAAGGTTTACAAATCTTATCATGTCTTTGAAATTCTTTTTGAAGTACCTACACCTAAAGAACCAGAGAAACCAAAACCTGCTTCAAAAGAAGAACCAGTACCAATTGTCCTACCAGCGGAAGGTACTAAAATAGAAACACTTCTTCATAAATATCTTTACTAAAATATATATCTTTGAAAAATGATCTTTAATGAAAAAATGAAAATGCTTCTAAAAAAAGGTAGGTAATAACATGCTTCTATGTATGTCATGTGTCTTGCATGAGAATCTTATATGTGTAAGATGCACACAGCATTCCTATTCCACTCAATAAAGAGGGGTGCCTTTATCTCACACAACCAATTACTCACAAATGATAATATCAAAGTATGCCTAAATAGATTTATGCTGTGCATACTAAATCAAAGCTCTTATTTGTAGATTTTGAATTTTTATATTTTAGACTCTTTTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41536
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 10499 | 31319 | 100 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44063638)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43188808 |
GRCz11 | 9 | 42990595 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAGGGTAAAGGAAAGATTCCATCTAAAGACCAGGACCCTGAGAAAGTT[C/T]AACTAAAACCTTTTACGAAGAAGCCTTCAGCTGGATCACCTAAAGAAAAG
Long Flanking Sequence:
ACCGAGCACCACCTGAGATAAAACCAGAAAGTGAAGTAGAAGACAAAGCAAAGAAAACAGCAGTTGCGAGGGTTCCAAAAAAAGTCACACCAGAGGAGCCTGGCTTAGCACTAAAAAAGGTTAAAAAGTTACCATTAGACACAGGAGAACCTGAATCTGTCAAATTAAAGCCGTTTGAAAAACCTGTGAAAACGCATCCTGAAACCGAGAAAGACACCAAAAAAGACGAAAAAGGAAGGGAACCTGCAACTTTTGACAAAAGTAGGGAACCGATTACTTTTCAGAAAGGAGAGCTGCCTTTAAAGGATGAGAAGACAAAGGAACCAGATGTGCCTGTGAAAAAAGAAAAGCCTTCTATTCCTGACAAAAAGGAGCCAGATGAAGTCGCTGTTAAAGCTGTAACCAGACCTGCAAAAGATGAAGTCCCTACAGAGCCTAAAGAGAAATTAGTTAAGGGTAAAGGAAAGATTCCATCTAAAGACCAGGACCCTGAGAAAGTT[C/T]AACTAAAACCTTTTACGAAGAAGCCTTCAGCTGGATCACCTAAAGAAAAGGAGGCCGCAGAGCCAAAAGACAGAAAACCAATTGAGTTGTCACCGCTAAGTAGGGCACCAAAAGATGATATTAAAAAAGAGCCAAGTATTCCAACCAAAAAAATTGACAGTCAAGAAACTCCAGACAAAGCTAAAGAGGTTGAGAAGATTTCAACTCCAGTCCCTGTAGAAGACAAAACGACACCTCCTAAAAAGGTTACCCCGGTAAAGAAGATTACACCCAAGGAAGATGAGAAGAAGCCTATTGTTATCAAAAAAGGTGTTTTACCCAAGGAGGCTGAGGAGAAAGAAGAAATAAAACTAAAACCAGTTGAACGTACAAAGAGTGGAATAGAGCCTGAAAAGATTCCTTCACCCAAGGTTGAGAAAACAAAGCCAGCTGAATCAGTTCCTGTACAGAGGAAACCTATTGATGATTTAACAAAAACACCAAAGACAATTTCACCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41535
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 10749 | 31319 | 100 | 230 |
ENSDART00000126871 | None | None | 22089 | None | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44062888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43188058 |
GRCz11 | 9 | 42989845 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAATATGAAGATGAAGAAGAAGAAGCATGGGGATGGGAGCTTGCTTCT[C/T]GAGACAGTTATGGTTCAGAGGGCTCTGAAGAACAATATTTGGAGGAAGGG
Long Flanking Sequence:
CCCCGGTAAAGAAGATTACACCCAAGGAAGATGAGAAGAAGCCTATTGTTATCAAAAAAGGTGTTTTACCCAAGGAGGCTGAGGAGAAAGAAGAAATAAAACTAAAACCAGTTGAACGTACAAAGAGTGGAATAGAGCCTGAAAAGATTCCTTCACCCAAGGTTGAGAAAACAAAGCCAGCTGAATCAGTTCCTGTACAGAGGAAACCTATTGATGATTTAACAAAAACACCAAAGACAATTTCACCAAAAGACTCAACTGAAGCAGTTATCTTGAAAAAAGTACCGCATAAGATTTCACCCAAGCAGGAAAAATCTGAGGAAACTCCTCAGATTTCTGGAGACGACAAGATACCAGTCCTGAAGGAGCTATCTCCGGGAGCTGTAGAGTTAAGAAAAGTCTCAACTCAGTTTGAGGAAGAAGTATTTGAAGAAGAGTTTGAATATGAAGCTGAATATGAAGATGAAGAAGAAGAAGCATGGGGATGGGAGCTTGCTTCT[C/T]GAGACAGTTATGGTTCAGAGGGCTCTGAAGAACAATATTTGGAGGAAGGGGCACTTGAGACTCCTGGAATGCCAGGGGGTAGACGAGGTGAGAGGGTCCCTGTAAACTACATCAATGAATGCCTCATTTTCCGTGGTATGGACATCAGCGCCCTGTTGTCATTTTTTTTTCATCCCAGATAATTCCCATGTCTTCATCCATGTCTGTTCACTTACTGTAAATCTTGTGCCTCCCTCTTCATCTTCTTCAGTCTTCATTGTGGCATGTGTTTTGTATTGTATTTAATGTCTTTCATCTTGTTTGTTGTTTGTCTGTGTCTTCATTGAGCTATAAATATAACTACTGGTGGAAAAATTGTCATTTTGTTGGGATCATAATTTGTCATCTAACTTGCCATAAATTGGAAGCATGATTTTATCATCTTCATGACCCTTCATTAATATTTCCCTTTTTTACTTAAGCGTTTCATTACTAGATATTTTAATTTAACTTCAAATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21578
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 10969 | 31319 | 102 | 230 |
ENSDART00000126871 | Nonsense | 207 | 22089 | 3 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44061445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43186615 |
GRCz11 | 9 | 42988402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTCAAGCAAATTGCTGGCAAAGTTCAAGTCAATGTTATTGGACTGCAG[C/T]GATCAGCAACGATCCAGGACACCAATGATGATGATGCTGGTGTTTATACC
Long Flanking Sequence:
TTGAGTGCCAGATCTCTCCGTCTACTGCTATCACCACCTGGATGAAAGATGGAAGCAATCTAAGGGAGAGTCCAAAGCACAAATTCACATCTGATGGCAAAGATCGCAAGCTGCAAATCATTGATGTACAGCTTTCAGACACTGGAGAGTACACGTGTGTTGCAAAGCTTGGCAACAAGGAGAAGACCTCAACTGCTAAGCTTATTGTTGAAGGTTGTGCATTAATCATGAATAAAAATAATGAGTAAGAAGTTAAAATTAAATACAAACAAAAACACTACCCCATGAGATTTAATGAGATTTTCTTCTGTTTATTTGGTTTAATAGAATTACCAGTGAAATTTACTAAGACTCTGGAGGAGGAAATGTCTGTGATTAAGGGACAGCCGATGTACTTAACCTGTGAGTTGAGCAAGGACAGAGATGTGGTCTGGAAGAAGAACGGAAAAGAGCTCAAGCAAATTGCTGGCAAAGTTCAAGTCAATGTTATTGGACTGCAG[C/T]GATCAGCAACGATCCAGGACACCAATGATGATGATGCTGGTGTTTATACCTGCGAGTGCGAAGACATCAAAACACAAGCCAATGTCAAAATTATAGGTATGCCTACAGAAATTCTTTATGGTTGTTTAAATAAAATGTAATTCTATACCACAATAAAATCACTAAATATCTATTGCAGAAATAATCAGAGATTGGTTGACAAAACCTTTGAGGGACCAGCATGTAAAACCAAAAGCTACCGCCACATTCAAATGTGAACTCTACAAGGACACTCCCAACTGGAAGTGGTTCAAGGGAGATGAAGAAATTCCCACTGACCCTACGAACAAGACTGATGTCAAAAAAGATGGCAAAGAGATCACACTTACAGTCAAGAATGCTCAACCTGATGATATTGGAGAGTATGCCATAGAAGTTGAGGGCCGCAGATATACAGCAAAACTCACTCTCGGAGGTCTGTTTAAAAGTATTTAAATTAATTTTCTTATTGAAGAAGATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12350
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 11026 | 31319 | 103 | 230 |
ENSDART00000126871 | Nonsense | 264 | 22089 | 4 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44061190)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43186360 |
GRCz11 | 9 | 42988147 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCWTTGAGGGACCAGCATGTAAAACCAAAAGCTACCGCCACATTCAAATG[T/A]GAACTCTACAAGGACACTCCCAACTGGAAGTGGTTCAAGGGAGATGAAGA
Long Flanking Sequence:
AAATTAAATACAAACAAAAACACTACCCCATGAGATTTAATGAGATTTTCTTCTGTTTATTTGGTTTAATAGAATTACCAGTGAAATTTACTAAGACTCTGGAGGAGGAAATGTCTGTGATTAAGGGACAGCCGATGTACTTAACCTGTGAGTTGAGCAAGGACAGAGATGTGGTCTGGAAGAAGAACGGAAAAGAGCTCAAGCAAATTGCTGGCAAAGTTCAAGTCAATGTTATTGGACTGCAGCGATCAGCAACGATCCAGGACACCAATGATGATGATGCTGGTGTTTATACCTGCGAGTGCGAAGACATCAAAACACAAGCCAATGTCAAAATTATAGGTATGCCTACAGAAATTCTTTATGGTTGTTTAAATAAAATGTAATTCTATACCACAATAAAATCACTAAATATCTATTGCAGAAATAATCAGAGATTGGTTGACAAAACCTTTGAGGGACCAGCATGTAAAACCAAAAGCTACCGCCACATTCAAATG[T/A]GAACTCTACAAGGACACTCCCAACTGGAAGTGGTTCAAGGGAGATGAAGAAATTCCCACTGACCCTACGAACAAGACTGATGTCAAAAAAGATGGCAAAGAGATCACACTTACAGTCAAGAATGCTCAACCTGATGATATTGGAGAGTATGCCATAGAAGTTGAGGGCCGCAGATATACAGCAAAACTCACTCTCGGAGGTCTGTTTAAAAGTATTTAAATTAATTTTCTTATTGAAGAAGATTGTTTTTGTTTTCTCTTAAATACTCTTTTTGTCTCAATTATATAGAGCGTGAAGCTGAGATTCTGAAGCCTCTTGCTAGTGTGGAGGTGGTTGAGAAAGGAGAAGCCAACTTTGATACTGAAATTTCAGAAGATGATATTCCTGGAGAATGGAAACTTAGAGGGCAGGTTCTGACAAGATCACCGGTAGGCTTGTATTTTGTTGAAGAGGCTCTGTCACTTTATATAATCTATTTTTTCCTCAGTAATTTTATAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30925
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 12176 | 31319 | 121 | 230 |
ENSDART00000126871 | Essential Splice Site | 1398 | 22089 | 22 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 12176 | 31319 | 121 | 230 |
ENSDART00000126871 | Essential Splice Site | 1398 | 22089 | 22 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44050615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43175785 |
GRCz11 | 9 | 42977572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACACATTAGTTTGTACATAATACTGATTGTACGATTTTTGTTACCAC[A/T]GAGGAGGAGGCTAGATTCACAAAGAACTTGGCTAACATTGAAGGCACTGA
Long Flanking Sequence:
TTGTATTTTTATCAACAGCTCCATATGTTGAGTTCACAAAGCCACTCCATGATGTTGAGGTCAAAGAGAAGGAATCTGCCAGATTTGAATGTGAAGTGTCTCGTGAGAGTGCAAAGGTTTGCCTTATATTAATTAGCTTTTTATAATCCAAATTCAAAATCAGTAAATGCATTATGCAAACTAGTGGCATTCTAAAACGATTATTAAAAGCTTATTTGGCTGAAAATTCCTATGTGCATTTTAAATAGGTTCGCTGGTTCAGAGATGGCAATGAAATCAGAAAAGGCAAGAAATACGAGATGATTTCTGAAGGAGTAAAACGCATTCTCATCATAAGCAAGTCTGTCTTTGATGATGAAGCAGAATATGAATGTGATGCCAGGACCTCCAAAAGCTCTGGCATGTTGACTGTCGTTGGTAAGTCCTGTTTATTTTCTGTCTATATATTTTTCAACACATTAGTTTGTACATAATACTGATTGTACGATTTTTGTTACCAC[A/T]GAGGAGGAGGCTAGATTCACAAAGAACTTGGCTAACATTGAAGGCACTGAAACCGACAGTGTTAAACTGATTTGTGAGGTTTCCAAACCCAGTGCAGAGGTTACATGGTACAAAGGTGACCAAGAATTGCCTGAAGTTGGTAGATATGAGCATATTACAGATGGCAAAAAGAGAATCCTCATTATTAAGGGTCTCCGTATGGATGATGCTGGAGAGTACCACTGTAAACTGCCCACCTCACAAACCACAGGAAACCTGAGGATTAATGGTACGACTTGTCCATGCAAACTGGCTTTATATCTCATAACATTTGTAAACATTGTTTTTATAAACTAACTTCATTTTTTCCCCTTAGAACTTGCCGCTGAGTTCATTGCCAGGCCTCAAAACCAAGAGGTGGTTGAAGGTGAAAAGGCACAATTTGTGTGCTCTGTCTCCAAAGACACATATGAAGTAAAATGGCTTAAAGGGAATACAGAACTTCAATCGGATGACAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41534
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 12176 | 31319 | 121 | 230 |
ENSDART00000126871 | Essential Splice Site | 1398 | 22089 | 22 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 12176 | 31319 | 121 | 230 |
ENSDART00000126871 | Essential Splice Site | 1398 | 22089 | 22 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44050615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43175785 |
GRCz11 | 9 | 42977572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACACATTAGTTTGTACATAATACTGATTGTACGATTTTTGTTACCAC[A/T]GAGGAGGAGGCTAGATTCACAAAGAACTTGGCTAACATTGAAGGCACTGA
Long Flanking Sequence:
TTGTATTTTTATCAACAGCTCCATATGTTGAGTTCACAAAGCCACTCCATGATGTTGAGGTCAAAGAGAAGGAATCTGCCAGATTTGAATGTGAAGTGTCTCGTGAGAGTGCAAAGGTTTGCCTTATATTAATTAGCTTTTTATAATCCAAATTCAAAATCAGTAAATGCATTATGCAAACTAGTGGCATTCTAAAACGATTATTAAAAGCTTATTTGGCTGAAAATTCCTATGTGCATTTTAAATAGGTTCGCTGGTTCAGAGATGGCAATGAAATCAGAAAAGGCAAGAAATACGAGATGATTTCTGAAGGAGTAAAACGCATTCTCATCATAAGCAAGTCTGTCTTTGATGATGAAGCAGAATATGAATGTGATGCCAGGACCTCCAAAAGCTCTGGCATGTTGACTGTCGTTGGTAAGTCCTGTTTATTTTCTGTCTATATATTTTTCAACACATTAGTTTGTACATAATACTGATTGTACGATTTTTGTTACCAC[A/T]GAGGAGGAGGCTAGATTCACAAAGAACTTGGCTAACATTGAAGGCACTGAAACCGACAGTGTTAAACTGATTTGTGAGGTTTCCAAACCCAGTGCAGAGGTTACATGGTACAAAGGTGACCAAGAATTGCCTGAAGTTGGTAGATATGAGCATATTACAGATGGCAAAAAGAGAATCCTCATTATTAAGGGTCTCCGTATGGATGATGCTGGAGAGTACCACTGTAAACTGCCCACCTCACAAACCACAGGAAACCTGAGGATTAATGGTACGACTTGTCCATGCAAACTGGCTTTATATCTCATAACATTTGTAAACATTGTTTTTATAAACTAACTTCATTTTTTCCCCTTAGAACTTGCCGCTGAGTTCATTGCCAGGCCTCAAAACCAAGAGGTGGTTGAAGGTGAAAAGGCACAATTTGTGTGCTCTGTCTCCAAAGACACATATGAAGTAAAATGGCTTAAAGGGAATACAGAACTTCAATCGGATGACAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31746
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 13381 | 31319 | 136 | 230 |
ENSDART00000126871 | Nonsense | 2603 | 22089 | 37 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44043783)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43168953 |
GRCz11 | 9 | 42970740 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGTCTCATTGAAGGACAGTGGTATGCTTATCGTGTGCGGGCTTTGAAC[A/T]AACTGGGTGCTAGTAAGCCTTGCAAGTCAACAGATGAGATCTTGGCTGTT
Long Flanking Sequence:
GTAATTGCCTGCAACAAATGTGGACCAGGTGAACCTGCCTACATTGAGGATCCAGTGAATGTGTCTTCACCTGCAAGTATGTGTCAATTCTACAAAGAGATCAGACAGTGTTAAACATTCACAATGTTAAATACATGAAAAACTCATCACTTATGTGTGTTCACAGCTGTACCAGACCCACCAGAAAATCTTAAATGGAGAGACAAGTCTGCTAGCAAAATCTTCTTGTCATGGGAGCCACCCAAGTGGGATGGTGGAACTCCTATCAAAGGTTATATTGTTGACAAATGTCAACGAGGCACTGACAAGTGGGAGCCATGTGGAGACCCTATGCCTGAGCTTAAGTGAGTGACCATTTTCAAAGTACTTATTCTGCAAACTTAATTGAGGTGAATGCATTACACCTCTAAATAATTATCTTAATCCTCTCTACAAACAGGTTCGAAGTCACTGGTCTCATTGAAGGACAGTGGTATGCTTATCGTGTGCGGGCTTTGAAC[A/T]AACTGGGTGCTAGTAAGCCTTGCAAGTCAACAGATGAGATCTTGGCTGTTGATCCTAAAGGTACTTTATCAGATTACGCTTTTACATTTTAGTCCATTTTGCTATTAAATTAGACTCTAAGTGGAACGTGTTATCCTTTTCCCTATTACTTTCACAGAGCCTCCTGAGATTCAGCTGGATGCAAAACTGCTAGCTGGTCTGACTGCTAAAGCTGGCACAAAGATTGAACTTCCAGCTGACATCACTGGTAAACCAGAGCCTAAAGTCAAATGGACCAAGGCTGACCTAGTCCTTAAGCCAGATGACAGAATCACCATTGATACAAAGCCTGGCCATTCAACTTTGTCCATCGCTAAGACCAAGAGGGATGACACAGCCACGTATATCATTGAGGCAGTCAACAGCAGTGGCCGTGCAACTGCAACTGTGGATGTCAACATTTTAGGTAGTGTGACTATAATATTTTATTGTTATATTTTAGAATTAGAGATTTTTTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38760
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 13557 | 31319 | 138 | 230 |
ENSDART00000126871 | Nonsense | 2779 | 22089 | 39 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44043051)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43168221 |
GRCz11 | 9 | 42970008 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAGTGAAATCTGGTACAAGCTGTCCTCCACTGTGAAGCAGACCACCTA[C/A]AAGGCCACCAAGCTTGTGGCTTTCAAGGAGTACATCTTTAGGGTGTATGC
Long Flanking Sequence:
CCAGCTGACATCACTGGTAAACCAGAGCCTAAAGTCAAATGGACCAAGGCTGACCTAGTCCTTAAGCCAGATGACAGAATCACCATTGATACAAAGCCTGGCCATTCAACTTTGTCCATCGCTAAGACCAAGAGGGATGACACAGCCACGTATATCATTGAGGCAGTCAACAGCAGTGGCCGTGCAACTGCAACTGTGGATGTCAACATTTTAGGTAGTGTGACTATAATATTTTATTGTTATATTTTAGAATTAGAGATTTTTTTTGTGATTAGTTTCTGGAAATGATTAATATCCAATCTTTACTAATCCCATGTAGATAAGCCTGGTCCTCCAGCTGCCTTTGACATCTCTGAAATTACCAATGAGTCCTGCGTGTTGGCTTGGAATCCTCCAAGAGATGATGGTGGGTCAAAGGTGACCAACTATATTGTTGAGAGGAAAGCTGTAGACAGTGAAATCTGGTACAAGCTGTCCTCCACTGTGAAGCAGACCACCTA[C/A]AAGGCCACCAAGCTTGTGGCTTTCAAGGAGTACATCTTTAGGGTGTATGCTGAAAATCAGTTTGGCATTGGTGCCCCAGCTGAACATGCCCCAATAATTGCCAGATACCCTTTCGGTATGTTGTTAAATGCCGTATCAACAATTTATCTATTTATTTTTTCCTAACATTTATTCAACATGAATTAGAAATTAATATGTATCTTCACATTATGATAGATACCCCTGGTCCTCCATACAAATTGGAACCATCGGATATTGCAAAGGATGCCGTAACTCTGTCCTGGTATGAGCCTGATGAGGATGGTGGAAGTCCTATTACTGGATATTGGGTAGAAAGATATGAGCCTGACCATGACAAATGGATCAGATGCAACAAGTTGCCTATCAGGGATACAAACTTTCGGTAATGTGAATTAGCCCTAGTAAGCCATTGCTTGTGTTTCATAAATGAAAATTTGTTAACATTCCTAAATAATCATTCACTTGCAGAGTGAAAGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10365
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 13632 | 31319 | 139 | 230 |
ENSDART00000126871 | Nonsense | 2854 | 22089 | 40 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44042725)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43167895 |
GRCz11 | 9 | 42969682 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTRTCYTGGTATGAGCCTGATGAGGATGGTGGAAGTCCTATTACTGGATA[T/G]TGGGTAGAAAGATATGAGCCTGACCATGACAAATGGATCAGATGCAACAA
Long Flanking Sequence:
TGGTCCTCCAGCTGCCTTTGACATCTCTGAAATTACCAATGAGTCCTGCGTGTTGGCTTGGAATCCTCCAAGAGATGATGGTGGGTCAAAGGTGACCAACTATATTGTTGAGAGGAAAGCTGTAGACAGTGAAATCTGGTACAAGCTGTCCTCCACTGTGAAGCAGACCACCTACAAGGCCACCAAGCTTGTGGCTTTCAAGGAGTACATCTTTAGGGTGTATGCTGAAAATCAGTTTGGCATTGGTGCCCCAGCTGAACATGCCCCAATAATTGCCAGATACCCTTTCGGTATGTTGTTAAATGCCGTATCAACAATTTATCTATTTATTTTTTCCTAACATTTATTCAACATGAATTAGAAATTAATATGTATCTTCACATTATGATAGATACCCCTGGTCCTCCATACAAATTGGAACCATCGGATATTGCAAAGGATGCCGTAACTCTGTCCTGGTATGAGCCTGATGAGGATGGTGGAAGTCCTATTACTGGATA[T/G]TGGGTAGAAAGATATGAGCCTGACCATGACAAATGGATCAGATGCAACAAGTTGCCTATCAGGGATACAAACTTTCGGTAATGTGAATTAGCCCTAGTAAGCCATTGCTTGTGTTTCATAAATGAAAATTTGTTAACATTCCTAAATAATCATTCACTTGCAGAGTGAAAGGACTACCCACAAGAAAGAAGTACAAGTTCCGTGTTTTGGCAGAGAATCTTGCTGGACCTGGAAAACCAAGCAAAGAGACAGACCAAATTTTGATTAAAGATCCAATTGGTAGGTTAAACATTGGATAAATATCGTGCTTTGTTTATTTTGACAAAATGATTACGTTATTCTTTATTTGAAGACAGCATACAGTATGAAGCTGATGTAAATCTTTATTTTAGATCCCCCATGGGCTCCTGGGAAGCCCACTGTTAAGGATGTAGCCAAAACCTCTGCTTTCCTGCAATGGACAAAGCCTGAACATGATGGTGGTGCAAAGATCGAGTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31745
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 104 | 17628 | 2 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 13800 | 31319 | 142 | 230 |
ENSDART00000126871 | Nonsense | 3022 | 22089 | 43 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44041787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43166957 |
GRCz11 | 9 | 42968744 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATGTATGACTTTTCTCAACAATTATCTTTCTCTTTTAGATCCTCCAT[C/G]ACCACCAAGATGGCTTCTAGTAGTTTCTAGTAGCAGGAACAGCGCTGAAC
Long Flanking Sequence:
AAACCTCTGCTTTCCTGCAATGGACAAAGCCTGAACATGATGGTGGTGCAAAGATCGAGTCTTACATTGTTGAGCTCCTCAAGAGTGGAACTGATGAGTGGGTCCGTGTAGCTGATAATATCCCCTCTCTTGAGCACTTCCTGAAGGGATTGATGGAAAAGCAAGAGTACTCATTCCGTGTCAGAGCTGTCAACGTAGCAGGCGAGAGTGAACCCAGTGAACCAAGTGATCCAGTGCTCTGCAAGGAGAGACTCAGTAAGTCATAAAGCTTGTTTTAGAGCTTAACGGTCACAATTTTTGTTGAAATGAGCACTTGCAATTTTTAATATTCTTTCAAGATATGATGGAAATTTATACAGGTTTAGATTAAATTAAGTTAATATGAAGTGACATTCTGTTATCAATTAGAGTTTAACTATTTGATTAGCATTTAACTGGTCAAGTGCATGATTCATGTATGACTTTTCTCAACAATTATCTTTCTCTTTTAGATCCTCCAT[C/G]ACCACCAAGATGGCTTCTAGTAGTTTCTAGTAGCAGGAACAGCGCTGAACTGAAATGGACTGCACCTGAGAGAGATGGTGGCTCTCCTATCACAAACTACATTGTTGAGAAGAGAGATGTCAGGCGCAAAGGCTGGCAGGCTGTGGACACCACAGTGAAGGAGCTGAAGTACACTGTCACCCCACTAAATGAAGGATCTCTATATGTGTTCCGTGTTGCTGCTGAAAATGCTGTAGGGCCGAGTGAATTTTGTGAACTTGAAGACTCTGTTCTTGCCAAGGATACTTTCGGTGCGTACTTAGTCTTTCTTATTTCTTACATTTTATTTTTTGAAGTGTATTATTGAATTTTTTTCACGTCTGCTTTTTTCCCTACAGGTACCCCTGGACCTCCATATAATCTGACTATCACTGAAGTTTCCAAGACTCATGTTGATCTGAAATGGGAAGCACCTCAGAATGATGGTGGAAGACCTGTTTTGAGGTAAAAAAAATACCGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45376
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 161 | 17628 | 2 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 13857 | 31319 | 142 | 230 |
ENSDART00000126871 | Nonsense | 3079 | 22089 | 43 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44041615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43166785 |
GRCz11 | 9 | 42968572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCGCAAAGGCTGGCAGGCTGTGGACACCACAGTGAAGGAGCTGAAGTA[C/A]ACTGTCACCCCACTAAATGAAGGATCTCTATATGTGTTCCGTGTTGCTGC
Long Flanking Sequence:
ATTCCGTGTCAGAGCTGTCAACGTAGCAGGCGAGAGTGAACCCAGTGAACCAAGTGATCCAGTGCTCTGCAAGGAGAGACTCAGTAAGTCATAAAGCTTGTTTTAGAGCTTAACGGTCACAATTTTTGTTGAAATGAGCACTTGCAATTTTTAATATTCTTTCAAGATATGATGGAAATTTATACAGGTTTAGATTAAATTAAGTTAATATGAAGTGACATTCTGTTATCAATTAGAGTTTAACTATTTGATTAGCATTTAACTGGTCAAGTGCATGATTCATGTATGACTTTTCTCAACAATTATCTTTCTCTTTTAGATCCTCCATCACCACCAAGATGGCTTCTAGTAGTTTCTAGTAGCAGGAACAGCGCTGAACTGAAATGGACTGCACCTGAGAGAGATGGTGGCTCTCCTATCACAAACTACATTGTTGAGAAGAGAGATGTCAGGCGCAAAGGCTGGCAGGCTGTGGACACCACAGTGAAGGAGCTGAAGTA[C/A]ACTGTCACCCCACTAAATGAAGGATCTCTATATGTGTTCCGTGTTGCTGCTGAAAATGCTGTAGGGCCGAGTGAATTTTGTGAACTTGAAGACTCTGTTCTTGCCAAGGATACTTTCGGTGCGTACTTAGTCTTTCTTATTTCTTACATTTTATTTTTTGAAGTGTATTATTGAATTTTTTTCACGTCTGCTTTTTTCCCTACAGGTACCCCTGGACCTCCATATAATCTGACTATCACTGAAGTTTCCAAGACTCATGTTGATCTGAAATGGGAAGCACCTCAGAATGATGGTGGAAGACCTGTTTTGAGGTAAAAAAAATACCGCTGGCTGGTGCAAATCAGTGTCAGCCCTATTCATACATCATAATATAGTATGCATTATATGGTACTAATTAGGGATGCTCATTTCGGTTAATTTTGCTAACCGACAACCGCCGCTCATTAATATATAATGAATAAATATAATATAATAATAAATATCATAATTCACGCACCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14025
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 557 | 17628 | 7 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 14253 | 31319 | 147 | 230 |
ENSDART00000126871 | Nonsense | 3475 | 22089 | 48 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44038191)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43163361 |
GRCz11 | 9 | 42965148 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAGCAGGCAGGAGAACCTATGTCAAAGTTATGTCTGGCGAAAACAAAK[T/A]GAGTTGGCCTGTAAAGGATCTCATTCAGAATGGAGAGTACTACTTCCGYG
Long Flanking Sequence:
ACAAAGATGGAAATGAAATGAAGGCTGATGACAGAACCTTCTTCAGAGCTGAGTACACATCCTGCCATCTGGAAGTTCCAAGCTGCTTACACGCTGATGCTGGCCAATACAAAGTTACCTTGGAAAACAGAAATGGTGCCACTAGTGGAACGATCAATGTTAAAGTTATTGGTATGTTTTAGTTTTCTGTATATCAGCTTCTTTATTGCAATATTTTATCTGTGTGTAATGACTGATTATGCTGACAAAACAGTGAAAATGTGTACATTTTAAACCAATGCTACATTTGCTTTGATTATAATTATAATGTTTTCTGCAATTGTCAGGTCTTCCTGGACCATGTAAAGATATTGTTGCTAGTGAAATTACCAAGAGCTCCTGCAAGGTGTCCTGGGAACCTCCAGACTATGATGGTGGTAGCCCTATTCTCCACTACGTGCTGCAACGCAGAGAAGCAGGCAGGAGAACCTATGTCAAAGTTATGTCTGGCGAAAACAAAT[T/A]GAGTTGGCCTGTAAAGGATCTCATTCAGAATGGAGAGTACTACTTCCGTGTCAGAGCTGTCAACAAGATTGGTGGTGGTGAATTTATTGAGCTTCGCAACCCTGTAATTGCAGAAGATCAGAAACGTATGTATAGTGGGATTCTGTGAAAGCATGTTGTATCTACTTTTCATTTTACATAACTTTTTTTTATCACATTCTTTTCTTCAAAAATACAGAACGTCCTGATCCACCAGTTGATGTGGAAACCCATAACCCAACATCTGAGAGTGTTACCCTTACTTGGAAGCCTCCCATGTATGATGGTGGAAGCAAAATTATGGGTTACATTCTTGAGAAGATGATGAAAGGGGAAGAGAACTTCCAGAGATGCAATGACTTCCTTGTGCCGGTGTTGTCTTATACTGTTAAGGGGTTGACACATGAAAAACAATATCAGTTCCGGGTTCGTGCAGAGAATGCAGCTGGTGTCAGTGATCCTTCTCGCAGCACACCTTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21577
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 671 | 17628 | 8 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 14367 | 31319 | 148 | 230 |
ENSDART00000126871 | Nonsense | 3589 | 22089 | 49 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44037756)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43162926 |
GRCz11 | 9 | 42964713 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCCGGTGTTGTCTTATACTGTTAAGGGGTTGACACATGAAAAACAATA[T/A]CAGTTCCGGGTTCGTGCAGAGAATGCAGCTGGTGTCAGTGATCCTTCTCG
Long Flanking Sequence:
CGTGCTGCAACGCAGAGAAGCAGGCAGGAGAACCTATGTCAAAGTTATGTCTGGCGAAAACAAATTGAGTTGGCCTGTAAAGGATCTCATTCAGAATGGAGAGTACTACTTCCGTGTCAGAGCTGTCAACAAGATTGGTGGTGGTGAATTTATTGAGCTTCGCAACCCTGTAATTGCAGAAGATCAGAAACGTATGTATAGTGGGATTCTGTGAAAGCATGTTGTATCTACTTTTCATTTTACATAACTTTTTTTTATCACATTCTTTTCTTCAAAAATACAGAACGTCCTGATCCACCAGTTGATGTGGAAACCCATAACCCAACATCTGAGAGTGTTACCCTTACTTGGAAGCCTCCCATGTATGATGGTGGAAGCAAAATTATGGGTTACATTCTTGAGAAGATGATGAAAGGGGAAGAGAACTTCCAGAGATGCAATGACTTCCTTGTGCCGGTGTTGTCTTATACTGTTAAGGGGTTGACACATGAAAAACAATA[T/A]CAGTTCCGGGTTCGTGCAGAGAATGCAGCTGGTGTCAGTGATCCTTCTCGCAGCACACCTTTGATCAAAGCCACAGATGCAACTGGTATGAACTTTTGTTACTTTTTAGCAAATCTTAAGTCCCTCTGAAGCAAATCGTTGGTATATTTAAACATTCTTTGGTATTTTGCTTCCAGATCGTCCTAAGGTATTCCTTAGCGGTAGTCTACAATCAGGCTTGGCTGTGAAACGAGGTGAAGAAATCAGATTGGATGCCAACATCTCTGGATTTCCCTACCCCCAAATTACATGGATGAGGAACAATGCAACAATTTGGCCAGAACCACTAAAGAAGAGGCCAGAAAGGCCCATTAAGAAGAAGAAGGAAAAGGAGGAAAAGAAGGAGGAGGGAGCAGAAAAGAAAGAGGCAGATGCAGAAAAGAAGGAGGAAGACAAAGAGGCAAAGGAGGAGGACAAAGAAAAGAAAGAGGAAAAGAAGGAGGAAGAAAAGGAAAAAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34744
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 718 | 17628 | 9 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 14414 | 31319 | 149 | 230 |
ENSDART00000126871 | Nonsense | 3636 | 22089 | 50 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44037526)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43162696 |
GRCz11 | 9 | 42964483 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCTAAGGTATTCCTTAGCGGTAGTCTACAATCAGGCTTGGCTGTGAAA[C/T]GAGGTGAAGAAATCAGATTGGATGCCAACATCTCTGGATTTCCCTACCCC
Long Flanking Sequence:
CTTTTCATTTTACATAACTTTTTTTTATCACATTCTTTTCTTCAAAAATACAGAACGTCCTGATCCACCAGTTGATGTGGAAACCCATAACCCAACATCTGAGAGTGTTACCCTTACTTGGAAGCCTCCCATGTATGATGGTGGAAGCAAAATTATGGGTTACATTCTTGAGAAGATGATGAAAGGGGAAGAGAACTTCCAGAGATGCAATGACTTCCTTGTGCCGGTGTTGTCTTATACTGTTAAGGGGTTGACACATGAAAAACAATATCAGTTCCGGGTTCGTGCAGAGAATGCAGCTGGTGTCAGTGATCCTTCTCGCAGCACACCTTTGATCAAAGCCACAGATGCAACTGGTATGAACTTTTGTTACTTTTTAGCAAATCTTAAGTCCCTCTGAAGCAAATCGTTGGTATATTTAAACATTCTTTGGTATTTTGCTTCCAGATCGTCCTAAGGTATTCCTTAGCGGTAGTCTACAATCAGGCTTGGCTGTGAAA[C/T]GAGGTGAAGAAATCAGATTGGATGCCAACATCTCTGGATTTCCCTACCCCCAAATTACATGGATGAGGAACAATGCAACAATTTGGCCAGAACCACTAAAGAAGAGGCCAGAAAGGCCCATTAAGAAGAAGAAGGAAAAGGAGGAAAAGAAGGAGGAGGGAGCAGAAAAGAAAGAGGCAGATGCAGAAAAGAAGGAGGAAGACAAAGAGGCAAAGGAGGAGGACAAAGAAAAGAAAGAGGAAAAGAAGGAGGAAGAAAAGGAAAAAGAAAAGGAGGTGGAGGAACCCGAAGAGCCTGAAGAAGAATACCATCCAAGCTTAAATGAACGTCTTACCATTGAATCAAAGAGAAAGGGTGAATCCTATATTATTATAAAAGATACTATCAGAGGCGATCATGGTGTTTTCACAATAAAAGTGGAAAATGATCATGGAACTGCCTCTGCCTCCTGTGAAGTTAATATCCTTGGTGAGTGTTTTTCTTATTGAGATATGGTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41533
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 1469 | 17628 | 16 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 15179 | 31319 | 156 | 230 |
ENSDART00000126871 | Nonsense | 4385 | 22089 | 57 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44034506)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43159676 |
GRCz11 | 9 | 42961463 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATATAGTGGCTCCAAGTTTGCGTATGCTGAAACACTTCAAGGGTGATT[T/A]GATTCGAGTAAGGAAAAATGAGCCTATTGAGATGCCTGCAGAAGTCACTG
Long Flanking Sequence:
TTGCTGTATTAAAAGCACTCAGTATTATGACTGTTCCCATGTGCTCACTGCCAAATGTTTATTGAATGACAGGTCCACCAACTTCTCCTGAAAAGTTCCACTATACAGAGAGAACCAAGTCCTCTGTTACAATTGAATGGAGGCCTCCCCGTAATGATGGTGGTAGTCCAATCATTGGCTACATCATTGAGAAAAAGCGACAAGATCAACCGGCCTTCCAGCGGGTCAACCCAGAGCTGTGCACTGTTCAAATTATGACAGTTGACAATCTAGATGAGCTTCATATGTATGAGTTCCGTGCAAAGGCTGTCAATGCATTTGGTGAAAGTGAGCCTTCAATAACCATGACTGTTGTCATTCAGGATGATGAAGGTATGTCCTTGTTGAACACCACTATTCCTCACACAGTTTTCAGATGTCTTACTACATGCATTTCATGTGTCTTTTAATGAATATAGTGGCTCCAAGTTTGCGTATGCTGAAACACTTCAAGGGTGATT[T/A]GATTCGAGTAAGGAAAAATGAGCCTATTGAGATGCCTGCAGAAGTCACTGGTTTGCCAATGCCAAAGATTGAATGGCTGAAGGATGATGTTGTTATTGAAAAGCCTACTGAGAAACTTCTATTTGAAACCAAAGAGATTGACAGAGTGACGTCACATACAAAACTGTCCATTCCTGGTGTTACAAGACTAGACAAGGGCACATACACTGTTACTGCCTCCAATCGTTTGGGAACGCTGAGTCATTCGGTCACAGTGGAAGTGTTGGGTAAGTTATGATATACTGTACAACAATAAGTATTATAACTCACATTTAAAACCATTTTAAATGATGACATAATATTTTCTTAATCAATGTCTTGCTGTAAGTTTAGAGTGTTTGCTTATTTTACATTGTCTTAATCACTTGATCATGTCTCTTTTCCTAGATCGCCCAACGCCACCAAGAAATGTTGCTGTTTCAAGCATCAAAGCTGAGTCTTGCAACCTTAGTTGGGATGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41532
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Essential Splice Site | 1558 | 17628 | 16 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 15268 | 31319 | 156 | 230 |
ENSDART00000126871 | Essential Splice Site | 4474 | 22089 | 57 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44034238)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43159408 |
GRCz11 | 9 | 42961195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCAATCGTTTGGGAACGCTGAGTCATTCGGTCACAGTGGAAGTGTTGGG[T/G]AAGTTATGATATACTGTACAACAATAAGTATTATAACTCACATTTAAAAC
Long Flanking Sequence:
TCTAGATGAGCTTCATATGTATGAGTTCCGTGCAAAGGCTGTCAATGCATTTGGTGAAAGTGAGCCTTCAATAACCATGACTGTTGTCATTCAGGATGATGAAGGTATGTCCTTGTTGAACACCACTATTCCTCACACAGTTTTCAGATGTCTTACTACATGCATTTCATGTGTCTTTTAATGAATATAGTGGCTCCAAGTTTGCGTATGCTGAAACACTTCAAGGGTGATTTGATTCGAGTAAGGAAAAATGAGCCTATTGAGATGCCTGCAGAAGTCACTGGTTTGCCAATGCCAAAGATTGAATGGCTGAAGGATGATGTTGTTATTGAAAAGCCTACTGAGAAACTTCTATTTGAAACCAAAGAGATTGACAGAGTGACGTCACATACAAAACTGTCCATTCCTGGTGTTACAAGACTAGACAAGGGCACATACACTGTTACTGCCTCCAATCGTTTGGGAACGCTGAGTCATTCGGTCACAGTGGAAGTGTTGGG[T/G]AAGTTATGATATACTGTACAACAATAAGTATTATAACTCACATTTAAAACCATTTTAAATGATGACATAATATTTTCTTAATCAATGTCTTGCTGTAAGTTTAGAGTGTTTGCTTATTTTACATTGTCTTAATCACTTGATCATGTCTCTTTTCCTAGATCGCCCAACGCCACCAAGAAATGTTGCTGTTTCAAGCATCAAAGCTGAGTCTTGCAACCTTAGTTGGGATGCCCCATTGGATATAGGTGGCAGTGAGCTTACCAACTACATTGTTGAGATGAAAGACCTTAATGTTGAAGATCCTGAAAAGGCTGAGTGGGTGCAAGTTACTAAGTCTATTATTGAAAAGAGATATGGGGTAAGAAAAAGATATATTTCAAATCCTTTTTGTATTTTGTCATTCAAATTATATCAAAATGGATATTTATTGTACAACACAAGTTGTGCTATGGTGTTGTTTATATTTTAAGTTACATAAAAATTGTGGTTTTTGCAGGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41531
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 1845 | 17628 | 19 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 15555 | 31319 | 159 | 230 |
ENSDART00000126871 | Nonsense | 4761 | 22089 | 60 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44032992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43158162 |
GRCz11 | 9 | 42959949 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACTGTGTTCACCATTCCAAACCTCCCAGAACTTAAGAAATACAGATTC[A/T]GAATCATTGCAGTCAATGAAATTGGAGAGTCTGAGCCTAGTCCCAGAACC
Long Flanking Sequence:
TCGTATTGGTCTCGTGTGAATAAGATCCTGGTTTCAAAACGTGGCATGAAAGGCTGGGAATACCAGGTTACACGTCTCTTTGAGGGAGTAGAGTATGAATTCCGTGCAATGGCTTGCAATTCTGCTGGTATTGGGCCACCTAGTGCCATCTCTGAGTCTGCTGTTGCTGACGATCCCCTGAGTAAGAGCATAATTTAAATGCATTTTTTAAATTTTGTATTGAAGGCTTTTTTTAATTGTACATCATGGTCTATGTTTGTGTGTGTACAGCTCCACCTAGCATGCCTGCAGCTCCTGAGATTGCTGACAAAACCAAGCATAGTGTCACCCTTGCATGGACCCCACCAGCTAAAGATGGTGGCCGCCCCATCAAGGGTTACATTATTGAGATTCAAGATGAAGGTACTTCTGAGTGGGCCAGGGTCAATGATGCTGAAAATCTACATCCTTCTACTGTGTTCACCATTCCAAACCTCCCAGAACTTAAGAAATACAGATTC[A/T]GAATCATTGCAGTCAATGAAATTGGAGAGTCTGAGCCTAGTCCCAGAACCAGCGAAGTTCGCATAGAAGATATTAAAAGTAAATGTCTCACTTTTTTTTAAAACGTAAATGTAATTAAGCATCTTCCAGAGTCATTTTCTTGACCTTATGCTCTCTCTTAAATTCACAGCTGCACCAAAGATCTTCATGGATATCAGTGCTGATGAACTGCTGTGTGTTCGGGCTGGAACTCCATTTAAGATTCCAGCTACCATCACAGGACGTCCCGCTCCTAAAGTTACATGGGAATTTGATGGAAAAGCAAAGACAGAAAAGAAGGATCGTCTCCATATTTTACCAGTAGATTCACAGGTAACATATTTCCCTAATTTTAGACACAAATAAATAGATTTTAATCTTTGATTTCATTTATGACTATGATTTTTCTTGGCCAACAGGTTGAATCTACAGATACCACTTCAGTTGTTACAGTTCCTGTGAGTTTGAGAAGTCATTCTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1736
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 2130 | 17628 | 23 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 15840 | 31319 | 163 | 230 |
ENSDART00000126871 | Nonsense | 5046 | 22089 | 64 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44031093)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43156263 |
GRCz11 | 9 | 42958050 |
KASP Assay ID:
554-1681.1 (used for ordering genotyping assays)
KASP Sequence:
TTGAACGTCTGAGCTGGGACACAAGTGGTCCACAGAAAGAGACTTGGAAA[C/T]AGTGCAACAAGAGAGATGTTGAAGAGACTACCTTCATCATTGAAGACCTT
Long Flanking Sequence:
TTGCCGGATAACGATGGTGGTGAGAGAATCAAGAGTTACTTTATTGAGAAGAAGGCTGTTAATGGAAAGGCTTGGACGGTTGCCAATGCTACTTGTGCCAGCATGGCCTTTGTCGTGTCCAACCTCCTTGAGGGACAGGACTACTTTTTCCGTGTTCGTGCGGAGAATCGCCTTGGATTTGGACCATTTACAGAGACTACAGAACCTGTTCGGGCTAGGGATCCTATTTGTAAGTTGGTTTACCCAATGTTTTCAACATTTTTACACATGCATTTTTGTTTAATTTTATAATTAAATTTGTTATTAACAATATATATTTTTTCTTTTGAAATAAAGATCCTCCCGATCCTCCAACCAAAGTTAAAATTAACCTTGTTACCAAAAATACTGTTACCCTTACATGGGTGCCTCCCAAGAATGATGGTGGTGCACCAGTAAAGCATTACATTATTGAACGTCTGAGCTGGGACACAAGTGGTCCACAGAAAGAGACTTGGAAA[C/T]AGTGCAACAAGAGAGATGTTGAAGAGACTACCTTCATCATTGAAGACCTTAAAGAGGGTGGCGAGTATGAGTTCCGTGTTAAAGCTGTAAATGAAGCTGGTGCAAGCAGACCTTCTGTTACCGCTGGACCAATTGTCATTAAGGACCAGACATGTGAGTAAATGGGTCATGTTATTGTTTTGCTATTTTAAAAAAGTTATGTTTTATTTATTTGCTTTTTCTTTGAAACGTTTTAGGTGCTCCAAGTATTGATCTCAGAGAGGCTTTGGAAGGCGCAGAAGGATTTGATGTCAACATTGTTGCCAGGATTCAAGGCTGTCCATTCCCATCTCTTGTCTGGCACAAAGCTCCACAAGACAAGCCTGATGACAAAGTTCCTGTACAGTATGACAAACATGTCAATAAACTTGTCTCTGATGAAAAATGCAGCCTGTTTATCCAGCAGTCAAAGAGAGATGACAGCGCAATGTACACACTCACAGCAACCAACAGCTTGGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41530
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Essential Splice Site | 2380 | 17628 | 25 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 16090 | 31319 | 165 | 230 |
ENSDART00000126871 | Essential Splice Site | 5296 | 22089 | 66 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44030160)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43155330 |
GRCz11 | 9 | 42957117 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGGACCACCTTTGTACAGTGAACCCGAGAAAGCACGAAATCTCTTCAG[T/G]AAGTTTTATTCACCAAAACCTCTAAATTTGCCTTGTGGACCGTGTGTTTA
Long Flanking Sequence:
GTTTATCCAGCAGTCAAAGAGAGATGACAGCGCAATGTACACACTCACAGCAACCAACAGCTTGGGCACAGCCACCAAGAGCATTAAGCTCAGCATTTTGGGTAAGTTCTTAATTGTCATGGGTTTCATTTTCCCCTAATTTCTTAATTAATCTATTTCAAAGGTCAAAATAAATAATATTCTGTTTTTCTTTTCTTAGGACGTCCTGGTGTACCTGTAGGACCAATTAAGATTGGGGAAGTTTTTGCTGAAAGGATTGGCCTCTCCTGGAATCCACCAGCAGATGATGGTGGTTCCAAGATCACAAACTATGTTGTTGAAAAGCGTGAGGAAAACAGAAAAACATGGGTCCATGTCTCTAGTGATCCAAAGGAATGCCAGTACATAGTACAAAGGCTAACAGAGGGCCATGAATATGAGTTCCGTGTTATGGCTCAGAATAAATATGGAGTTGGACCACCTTTGTACAGTGAACCCGAGAAAGCACGAAATCTCTTCAG[T/G]AAGTTTTATTCACCAAAACCTCTAAATTTGCCTTGTGGACCGTGTGTTTATGCATGTATGATATAAATGGTTCATTGTATACAGTGCGAGGAGACCATTAAGCTTGAAAAATCATACAATAATTGTTTATGGACCAGCTCAGTGGTTAGTACTGCGCTTTGGGTTTTAGAAAAGCGCGTTATAAATAAAATATATTATTATTATTATTATTAATATTATTATTATTATTGCTGTTGCCTCACAGCAAAAAAAGTTACTGGTTTGAATTCAGGCTGGGCCAGATTGCATGTTCTCCCTGTTCGTGTGGGTTTCCTCTAGTTTCCCCCACAGTCCAAAGACATGTGACATAGGTAAATTGGATGGTCTAAATTGTAATTAAAAAGTGTGTGTGTGTGTGAGTGTGAATGAGAGAGTGTATGGGTGTTTCCTAGCGTGGTGCTGGGTTGCGACTGGAATTGTATTGGTTGCGTAAAACATATGGGTTAGTTTCACTATATCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34743
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 2698 | 17628 | 30 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 16408 | 31319 | 170 | 230 |
ENSDART00000126871 | Nonsense | 5719 | 22089 | 72 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44026694)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43151864 |
GRCz11 | 9 | 42953651 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATGTTGAGGTGACAGCCATCACAAATGATTCAATCAGTGTCGCATGG[A/T]GATCTCCAAAATATGATGGAGGGTCAGACATTACAAGCTATGTTCTTGAG
Long Flanking Sequence:
AAATATTTAAAATTGCCTCTTTTATTTATTCACAGATGTTCCTGGTCCTGTTGGTCTACCCTTCTCTGGTGAGAATCTTACCAATGACTCTTGTAAATTGACATGGTACTCCCCTGAAGATGATGGTGGCTCAGCTATCACCAACTATATAATTGAGAAGAGAGAAGCTGACCGCAGAGGCTGGACTTCAGTGACATATACTGTCACAAGACATAATGCTGTTGTCCAGGGTCTCATTGATGGAAAGGGTTACTTCTTCAGAATTGCAGCTGAAAATATAATTGGAATGGGTCCATTCACTGAGACTGCAGCTCCAGTCGTCATCAAGGATCCACTCTGTAAGCCTTTTTTGTTTTGTTTTTGAACAGTTTTTTTTTATTTTATTTCGAAATATCATTACCTTATATCATATCTTATGTTTTTTAACTCAAGCTGTACCCGAGCGCCCTGAGGATGTTGAGGTGACAGCCATCACAAATGATTCAATCAGTGTCGCATGG[A/T]GATCTCCAAAATATGATGGAGGGTCAGACATTACAAGCTATGTTCTTGAGGTTCGTCTAATCGGGCAGGACAACTTCAGCCGCATTGCCAAAGAGGACAAACTCATGGATCGTAAATTCACCCATGCTGGTCTTAAAGAGGGTTCTTCTTATGAATTCCGTGTTAGTGCTGTTAATCAAATTGGTCAAGGCAAACCGTCATTCAGCACAAAACCAGTTACATGCAAAAAAGAGTTTGGTAAGTAATTACTTTAAAGCAGAAGTGATTTCATAAAATTAAAGCACATTTTTATTAACTGTGATCGAGATCATATATTGTATACTATAATCTTTACTAGAACCACCAAACCTTGATTTGGAGTTCCGTGACAAGCTTGTTGTTCGTGTTGGGGAAACTTGCATCATTCAAAGCCGATACACAGGCAAACCGGAACCAACTATTAAGTGGTTCAAAAATGATGAAGAGCTTCAGGCAAATGAAGAAATTGCTCTTACCACTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8574
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 3447 | 17628 | 37 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 17173 | 31319 | 177 | 230 |
ENSDART00000126871 | Nonsense | 6468 | 22089 | 79 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44023560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43148730 |
GRCz11 | 9 | 42950517 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAATGCAATTGGTCTAAGTAGACCAGACACCACTGTGCCAGTTCTTTGT[C/T]AGGAAAAACTAGGTGACATTMACATTTTAACATCTAATATGTTTATTTAA
Long Flanking Sequence:
GTGAATATGTCGAGACAACAAAAGCTATCAAAGCAATGAATCCACTGTGTATGTATGGTCTATTAAAAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTGATAATGTTTAATTTATAAAAAGGATCATAATAAAAAAAACTAATAATAATATTTATTATTCACTTACAAATTTCAGTCCCACCTGGTCCACCAAAAGACCTTCATCATGTAGATGCTGACAAGACTGAGGTGTGGCTTCAGTGGAACTGGCCTGATCGCACAGGAGGAAGTGACATCACAGGGTTCTTGGTTGAGTATCAGGAAGAAGGTGAAAAGGATTGGATAGTTTTTAAGACTGTCAGCATTCCTGAGTGCCATGTGACAGGACTGGAAGAGGGAAAGACCTACAGGTTCCGTGTTAAGACGGAAAATGCAATTGGTCTAAGTAGACCAGACACCACTGTGCCAGTTCTTTGT[C/T]AGGAAAAACTAGGTGACATTCACATTTTAACATCTAATATGTTTATTTAAAGGAAATATGATTATGATTTGTATGTGTTAAACCTTTTTTTTATTGTCTGTTTTAATTCTTTTTAGTACCGCCCATTGTTGAGGTGGATGTTAAGTTGATTGAGGGAATCATTGTGAAAGCTGGAAGCACAATTAGATTGCCTGCTTTAATGAGAGGCCTTCCTGTTCCCACTGCTAAATGGGTCATTGATGGAGAGGAAATCAAGAGTGAAGGCAATACCAAAATTGACACTGACAACTTCTCCACTGTTTTGAGCATTGCAGACTGCACAAGAAATCACACTGGAATATATATACTCACAGTATCTAACTCTGCAGGAAGTAAAACTGTTTCTCTGAACGTCACTGTGCTTGACGTACCAGCTGCACCTATAGGCCCTGTTAATATTCTTGAGGTAACTCCTGACTCCATGGTTATTGACTGGCGCCCTCCCAAAGATGATGGTGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2512
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 3805 | 17628 | 38 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 17531 | 31319 | 178 | 230 |
ENSDART00000126871 | Nonsense | 6826 | 22089 | 80 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44022382)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43147552 |
GRCz11 | 9 | 42949339 |
KASP Assay ID:
554-3186.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAAGGAGGTGCTGAGTGGGAGAAAGTCAATAAGGATGATCTGATTAAA[C/T]AGTGTGCTTATAGGGTGAAAGGACTGACTGAAGACACTGAGTACAGGTTC
Long Flanking Sequence:
CACCAACTGTAGCTCGGCACCAGTTTGAGGCCCCTGGCCATCCTGGAAAACCTGTAGCTTCTGATTTGTCTGAAGATGCGCTTACACTTGGATGGACAATGCCTCTGTTTGATGGTGGCAGTCCAATCAGTGGTTACATTATTGAGCGAAGACATAAAGGTGGCAAATGGATTAGAGTGAATAAAACTCCTTGCAAAGAACTTAGATATAGAGTGCTTGGTCTTTTTGAAGGTAATGAATATGAGTTCAGAGTATTTGCTGAAAATATTGCTGGCTTTAGTGGACCTTCACCTGTCTCAGATCCTGCCAAACCTTGCAGACCAATAACTGTTCCAGGACCTCCAGTTAACCCTAAGGTAAAAGACTACAGCTGCACATATGCTGACTTAGTCTGGATCAAACCCACAAAAGATGGAGGCAGTCCAGTCTTGGGATATATTGTTGAATGCCAGAAAGGAGGTGCTGAGTGGGAGAAAGTCAATAAGGATGATCTGATTAAA[C/T]AGTGTGCTTATAGGGTGAAAGGACTGACTGAAGACACTGAGTACAGGTTCCGTGTTAAAGCTGTGAACATGATTGGAGAAGGTGAGACCAGAGAAATCCCAGAGTCCGTTATTGCTAAGGATATCATCATTCCTCCGGAAATTGAGATGGATGCCACATGCCATGAACGTGTGACTGTTCGTGTTGGTCATAACATTAATGTTGTAGGATATGTAAAAGCAAGACCTGATCCAGAAATCACTTGGAGCAAAGGTGAAAGCATTTTGGAAAGGGACAAGCGCACCATGCTTACAAACAACTTCCCAGTCGTGCAAATGCGTATCAAGGAAGCAACCAGAGCAGACCATGGAAAGTATGTACTAAAGGCTGTTAATGAAGCTGGAGAGGCCTCAGCAACTATTACAGTAAATGTTCTGGATAGACCTGGTCACTGCCAGAATCTAAAGATGACATATGTAACTAAGAATTCTTGCATGGTGTCCTGGGATGCTCCTGAGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21576
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 4162 | 17628 | 38 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 17888 | 31319 | 178 | 230 |
ENSDART00000126871 | Nonsense | 7183 | 22089 | 80 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44021310)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43146480 |
GRCz11 | 9 | 42948267 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTCTTGACATGAAATTTGTTGGCACTATTGTGGTCAAAGCAGGTGAAT[C/A]AGTTAGACTTGAAGCTGGACTTAGAGGAAAACCACAGCCCACGGTTACTT
Long Flanking Sequence:
CTCATCTGACTGCACAAATCGCATGGTAAAAGCCAAGCTCATGGAAAACCATGAATATTTATTCCGTGTGTCTGCTGAGAACAAGTGCGGTCCAGGACCAGCTACAGAAACCAAAACTCCTATCCTTGCAATTGACCCACTTCAGAAGCCAGGCGAGCCAGAGAATTTCCATGTCGGTGATATTGGTAAAAACTTTGTTTTCCTTAAATGGAGAAAACCAGATTATGATGGTGGCAGTCCTAACCTTGGCTACTATCTGGAGAGAAAAGCAAAAGACGCTGAAGCATGGGAGAAGTTACATGAAGGAGTTCTGAAAGAGACATTCTTCATGGTAGACAAATGTGTTGAGAACCACATCTATCAATTTAGAGTCCAGTCAACCAATGATGGAGGAGAAAGTGCATGGGTTAGCACTTCTGATATTGTCGTCAAAGAAGAAATTCAGAAACCAGTTCTTGACATGAAATTTGTTGGCACTATTGTGGTCAAAGCAGGTGAAT[C/A]AGTTAGACTTGAAGCTGGACTTAGAGGAAAACCACAGCCCACGGTTACTTGGGTGAAGGACAAGGCTACGGGTGATAATCCAAGGATCAGCATTGACACCGGACATGATTACTCCAAATTCCTTCTGACTAAAACCAAGCGTAGTGACACTGGAAAATATGTAGTTACTGCTACAAACCCAGCTGGTTCATTCACAGCATATGCCAACGTTACAGTGCTAGATATACCAGGACCTGTCAGAGATATGAAAATTTCTGGCATTTCCACAGACAAGTGCAGAGTTGCATGGGATCCTCCAGAGGATGATGGTGGTTGTGAAGTGGACAGCTATATAATAGAAAAATGTGAGACCAGAAGAATGGTTTGGTCCACTTACTCTGCATCTCTCGTCACAAACTACTGTAATGTAACACGCCTTGTTGAAGGAAATGAGTACATATTCAGGGTCAGAGCAGAAAACAAGATGGGAACTGGGCCACCAATGGAGAGCAGGCCTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1029
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 4517 | 17628 | 39 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 18243 | 31319 | 179 | 230 |
ENSDART00000126871 | Nonsense | 7538 | 22089 | 81 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44020147)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43145317 |
GRCz11 | 9 | 42947104 |
KASP Assay ID:
554-0933.1 (used for ordering genotyping assays)
KASP Sequence:
CTGGACAGCTTGTCTTAACTGAATACACAATCWGTAACTTGGATGAGAGA[C/T]AGGAATATGAATTCCGTGTGTCTGCTCAAAACCAAGTTGGTATGGGCCGT
Long Flanking Sequence:
GGGTCCCAGTCACAAAGAGCCCTATTTCTGAGAGACGTATGAAGGTTACTAATCTGATCCCTAACCACGATTATCAGTTCCGTGTCAAAGCTGAAAATGAAGTTGGATTGGGAGAACCAAGCAAAGCATCTAGACCCATCACTGCAAAAGATCCAATTGGTATGTGTAGGTTGGGTTATATATATGTATGTATTTTGTTTTATTAGATAATAATTTTATTGTGTTTTAAACTAAAACAACATTTTGTTTCATTTTTAGAGCCTCCTGGCCCTCCTGGTAGCCTTAAAGTAGTTGACAGCACAAAGACATCGATTACACTTAGCTGGGCAAAGCCTGTGTATGATGGTGGAGCTCCAGTTATTGGATATTTGGTTGAAATGAGGGATAAGGTGGAAATGGAAGGTGAACAAGTACGTGATCCAGAGGAAGGCTGGAAGAAATGCAATACTTCTGGACAGCTTGTCTTAACTGAATACACAATCAGTAACTTGGATGAGAGA[C/T]AGGAATATGAATTCCGTGTGTCTGCTCAAAACCAAGTTGGTATGGGCCGTCCTGCAAATGTCAAGGATGCTGTATCTCCAAAGGAGGTCCATGGTAAGTTTTGACAAGAGTCACATGTATGACTGCCCTTGAAGTTCAGTACATATATTCTTTTTTTCTTCTTTTACAACAGAACATCCAGAGATTGATCTTGATGCCAGTCTAAGAAAGGGTCTTAGTGTCAGAGCAGGATGTCCTATCAGACTTTTTGCTACAATAAGAGGAAGGCCAGCACCTAAAGTTACTTGGAAGCGCATTGGTGTTGACAATGTCATAAGGAGGGGTCACGTGGATCAGATTGATACAATGACCTTCCTCGTCATTCCCGAATCCTCACGAGAAGACTCTGGCAAATACTCTTTGACTCTTTCAAATCCCTCTGGAGAGAAGGCTGTGTTTGTCCGTGTCAAAGTCTTAGGTAATCTTCAAATTAAAATGCATTTTACAATTAAGATAGACAT
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
Stage | Entity | Quality | Tag |
---|---|---|---|
Hatching:Pec-fin ZFS:0000034 |
eye ZFA:0000107 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
Hatching:Pec-fin ZFS:0000034 |
head ZFA:0001114 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
Hatching:Pec-fin ZFS:0000034 |
inner ear ZFA:0000217 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
Hatching:Pec-fin ZFS:0000034 |
larval locomotory behavior GO:0008345 |
disrupted PATO:0001507 |
abnormal PATO:0000460 |
Hatching:Pec-fin ZFS:0000034 |
pericardium ZFA:0000054 |
edematous PATO:0001450 |
abnormal PATO:0000460 |
Hatching:Pec-fin ZFS:0000034 |
whole organism ZFA:0001094 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa21575
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 4646 | 17628 | 41 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 18372 | 31319 | 181 | 230 |
ENSDART00000126871 | Nonsense | 7667 | 22089 | 83 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44019595)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43144765 |
GRCz11 | 9 | 42946552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGTATCTTCTACAAAGTTGTTTCTGAAATTAATCAACAGATACTCCT[G/T]GACCTGTTGGTGGACTGGACGCAACTGATATCACAAAGACATCCTGCCAG
Long Flanking Sequence:
CTGCAAATGTCAAGGATGCTGTATCTCCAAAGGAGGTCCATGGTAAGTTTTGACAAGAGTCACATGTATGACTGCCCTTGAAGTTCAGTACATATATTCTTTTTTTCTTCTTTTACAACAGAACATCCAGAGATTGATCTTGATGCCAGTCTAAGAAAGGGTCTTAGTGTCAGAGCAGGATGTCCTATCAGACTTTTTGCTACAATAAGAGGAAGGCCAGCACCTAAAGTTACTTGGAAGCGCATTGGTGTTGACAATGTCATAAGGAGGGGTCACGTGGATCAGATTGATACAATGACCTTCCTCGTCATTCCCGAATCCTCACGAGAAGACTCTGGCAAATACTCTTTGACTCTTTCAAATCCCTCTGGAGAGAAGGCTGTGTTTGTCCGTGTCAAAGTCTTAGGTAATCTTCAAATTAAAATGCATTTTACAATTAAGATAGACATTGTGTGTATCTTCTACAAAGTTGTTTCTGAAATTAATCAACAGATACTCCT[G/T]GACCTGTTGGTGGACTGGACGCAACTGATATCACAAAGACATCCTGCCAGCTTGCATGGTTGCCTCCAGAAAATGATGGTGGTAGTCCAATCCTAAACTATATTGTTGAGAAGCGTGAAGTTGACAGGAAAACATGGACAAATTGCACAAACGATTTGAAGAAGACAAGTTTCAAAATCACAAATCTGACTCCAGGAATAGAGTACTACTTCCGAGTCATGGCAGTTAACAAGTATGGTATTGGGTTACCTCAAGACTCACCGAAATCATACTTGGCTACAGATCCTAAGAGTAAGTCCACCACAGTATTGTAATATATTGCATTGGATTATAATACTTTCAGTAAATAATGCATATATTTCTACTCTTCAAAGGTGAGCCTGATCCTCCAAAGAAGATGGATGTATTAGAAATTACTAAAAACAGCGCAACCCTTGGGTGGTTGAAACCACTCAGAGATGGTGGATCAAAAATTAATGGCTACATTGTTGAATACCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21574
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 4698 | 17628 | 41 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 18424 | 31319 | 181 | 230 |
ENSDART00000126871 | Nonsense | 7719 | 22089 | 83 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44019438)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43144608 |
GRCz11 | 9 | 42946395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGAAGCGTGAAGTTGACAGGAAAACATGGACAAATTGCACAAACGATT[T/A]GAAGAAGACAAGTTTCAAAATCACAAATCTGACTCCAGGAATAGAGTACT
Long Flanking Sequence:
AGGGTCTTAGTGTCAGAGCAGGATGTCCTATCAGACTTTTTGCTACAATAAGAGGAAGGCCAGCACCTAAAGTTACTTGGAAGCGCATTGGTGTTGACAATGTCATAAGGAGGGGTCACGTGGATCAGATTGATACAATGACCTTCCTCGTCATTCCCGAATCCTCACGAGAAGACTCTGGCAAATACTCTTTGACTCTTTCAAATCCCTCTGGAGAGAAGGCTGTGTTTGTCCGTGTCAAAGTCTTAGGTAATCTTCAAATTAAAATGCATTTTACAATTAAGATAGACATTGTGTGTATCTTCTACAAAGTTGTTTCTGAAATTAATCAACAGATACTCCTGGACCTGTTGGTGGACTGGACGCAACTGATATCACAAAGACATCCTGCCAGCTTGCATGGTTGCCTCCAGAAAATGATGGTGGTAGTCCAATCCTAAACTATATTGTTGAGAAGCGTGAAGTTGACAGGAAAACATGGACAAATTGCACAAACGATT[T/A]GAAGAAGACAAGTTTCAAAATCACAAATCTGACTCCAGGAATAGAGTACTACTTCCGAGTCATGGCAGTTAACAAGTATGGTATTGGGTTACCTCAAGACTCACCGAAATCATACTTGGCTACAGATCCTAAGAGTAAGTCCACCACAGTATTGTAATATATTGCATTGGATTATAATACTTTCAGTAAATAATGCATATATTTCTACTCTTCAAAGGTGAGCCTGATCCTCCAAAGAAGATGGATGTATTAGAAATTACTAAAAACAGCGCAACCCTTGGGTGGTTGAAACCACTCAGAGATGGTGGATCAAAAATTAATGGCTACATTGTTGAATACCAGCAGGATGGCCAACCTGAAGACAAGTGGACATCATACTCTGTTGTGAAAGACTTAACAATTGTTGTTGCTGGACTGAAAGAAAACACTAAATACAGGTTCAGGGTTGCAGCAAGAAATGCAATAGGATGCAGTTTGGCAAGAGAAGCTGAAGGCATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15885
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Essential Splice Site | 5636 | 17628 | 50 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 19362 | 31319 | 190 | 230 |
ENSDART00000126871 | Essential Splice Site | 8657 | 22089 | 92 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44014872)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43140042 |
GRCz11 | 9 | 42941829 |
KASP Assay ID:
554-6629.1 (used for ordering genotyping assays)
KASP Sequence:
GGTGAGCCAAGTGAAGTTCCTGAAAAACATTTGGCAAAGGATATCTTACG[T/G]AAGTAAATCTAACAACTGATTTTTTTTNNNNNNNNNAAAAGGAGTACAAT
Long Flanking Sequence:
TCAGAGTCATTGCACTAAATAAAGCTGGTCTTGGTAAACCAAGTGATCCATCATCTGGTGTTCTTGCTTTAGACCCAGTGTGTAAGTACTAACATTACTCCATTAATTATTATTAACAACCTGTTTGACAAAAAATAATGGCGTTTTACAGTTTGTGCATTGTAATCCATGCATTTCTGTGCTTTCATCATAGATCCTCCTGGACCACCTGCTTTTCCAAAGGTTGTTGACTCTACACACAGTTCAATCAGTTTGTCCTGGACCAAGCCCGCATATGACGGTGGATGTGAAATTCTGGGCTACCTTGTTGAATTCAAGCGAGCAGATGCAGAAGAATGGATGAAGTGCAATGTGCCAAAGAATCTCCAGGCAACAAAATTTAATGTTACTGGTCTAATAGATAATACTGAGTACCAGTTCCGTGTTAGTGCCGTAAACAAGATAGGATTTGGTGAGCCAAGTGAAGTTCCTGAAAAACATTTGGCAAAGGATATCTTACG[T/G]AAGTAAATCTAACAACTGATTTTTTTTATTTTTATTAAAAGGAGTACAATGTAGATTACACTTACATTATTTTAATGTTAATTTTCTTTTAGTTGCCCCTGAGGCTGAACTTGATGCTGATCTCAGAAAAGCACTTGTTTTACGTGCTGGAGTAACAATGAGAATTTACGTGCCTCTAAGAGGGCGTCCTGCTCCAAAGGCAACATGGACTAAGGTCAATGCAAATTTGAAAGAGAGGCAAGGTCTTATGATTAAGACAACTGAATGGGATACCTTCCTTTATTGTGAGGATATCAACAGATATGATGCTGGCAAATATGTTCTAACTTTAGAAAACAGTAGTGGTACCAAGTCATACACCATTGTTGTCAAAGTACTAGGTAAGACTCTCTTCTCTTAAAAAACATGCCATTTGAGTTTTAATCTTTGCTGTACCTAACTGTATTCAATAATGTGCACAGACACACCTGGACCTCCAGTCAATCTGATTGTTAAGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34742
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 5652 | 17628 | 51 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 19378 | 31319 | 191 | 230 |
ENSDART00000126871 | Nonsense | 8673 | 22089 | 93 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44014731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43139901 |
GRCz11 | 9 | 42941688 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTGCCCCTGAGGCTGAACTTGATGCTGATCTCAGAAAAGCACTTGTTT[T/A]ACGTGCTGGAGTAACAATGAGAATTTACGTGCCTCTAAGAGGGCGTCCTG
Long Flanking Sequence:
CGTTTTACAGTTTGTGCATTGTAATCCATGCATTTCTGTGCTTTCATCATAGATCCTCCTGGACCACCTGCTTTTCCAAAGGTTGTTGACTCTACACACAGTTCAATCAGTTTGTCCTGGACCAAGCCCGCATATGACGGTGGATGTGAAATTCTGGGCTACCTTGTTGAATTCAAGCGAGCAGATGCAGAAGAATGGATGAAGTGCAATGTGCCAAAGAATCTCCAGGCAACAAAATTTAATGTTACTGGTCTAATAGATAATACTGAGTACCAGTTCCGTGTTAGTGCCGTAAACAAGATAGGATTTGGTGAGCCAAGTGAAGTTCCTGAAAAACATTTGGCAAAGGATATCTTACGTAAGTAAATCTAACAACTGATTTTTTTTATTTTTATTAAAAGGAGTACAATGTAGATTACACTTACATTATTTTAATGTTAATTTTCTTTTAGTTGCCCCTGAGGCTGAACTTGATGCTGATCTCAGAAAAGCACTTGTTT[T/A]ACGTGCTGGAGTAACAATGAGAATTTACGTGCCTCTAAGAGGGCGTCCTGCTCCAAAGGCAACATGGACTAAGGTCAATGCAAATTTGAAAGAGAGGCAAGGTCTTATGATTAAGACAACTGAATGGGATACCTTCCTTTATTGTGAGGATATCAACAGATATGATGCTGGCAAATATGTTCTAACTTTAGAAAACAGTAGTGGTACCAAGTCATACACCATTGTTGTCAAAGTACTAGGTAAGACTCTCTTCTCTTAAAAAACATGCCATTTGAGTTTTAATCTTTGCTGTACCTAACTGTATTCAATAATGTGCACAGACACACCTGGACCTCCAGTCAATCTGATTGTTAAGGAGACCTCAAAGGACCATGTATCCATTACTTGGGATGCTCCATTAATTGATGGTGGAAGTCCAGTGAAGAGCTATGTGGTTGAAAAACGTCTGGCTGAGAGAAAGGCATGGACTTGTGTTGCTCCTGAGTGTCCCAAGACATCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45375
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Essential Splice Site | 5732 | 17628 | 51 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 19458 | 31319 | 191 | 230 |
ENSDART00000126871 | Essential Splice Site | 8753 | 22089 | 93 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44014490)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43139660 |
GRCz11 | 9 | 42941447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAACAGTAGTGGTACCAAGTCATACACCATTGTTGTCAAAGTACTAGG[T/C]AAGACTCTCTTCTCTTAAAAAACATGCCATTTGAGTTTTAATCTTTGCTG
Long Flanking Sequence:
ATGTTACTGGTCTAATAGATAATACTGAGTACCAGTTCCGTGTTAGTGCCGTAAACAAGATAGGATTTGGTGAGCCAAGTGAAGTTCCTGAAAAACATTTGGCAAAGGATATCTTACGTAAGTAAATCTAACAACTGATTTTTTTTATTTTTATTAAAAGGAGTACAATGTAGATTACACTTACATTATTTTAATGTTAATTTTCTTTTAGTTGCCCCTGAGGCTGAACTTGATGCTGATCTCAGAAAAGCACTTGTTTTACGTGCTGGAGTAACAATGAGAATTTACGTGCCTCTAAGAGGGCGTCCTGCTCCAAAGGCAACATGGACTAAGGTCAATGCAAATTTGAAAGAGAGGCAAGGTCTTATGATTAAGACAACTGAATGGGATACCTTCCTTTATTGTGAGGATATCAACAGATATGATGCTGGCAAATATGTTCTAACTTTAGAAAACAGTAGTGGTACCAAGTCATACACCATTGTTGTCAAAGTACTAGG[T/C]AAGACTCTCTTCTCTTAAAAAACATGCCATTTGAGTTTTAATCTTTGCTGTACCTAACTGTATTCAATAATGTGCACAGACACACCTGGACCTCCAGTCAATCTGATTGTTAAGGAGACCTCAAAGGACCATGTATCCATTACTTGGGATGCTCCATTAATTGATGGTGGAAGTCCAGTGAAGAGCTATGTGGTTGAAAAACGTCTGGCTGAGAGAAAGGCATGGACTTGTGTTGCTCCTGAGTGTCCCAAGACATCTTTTAGGATTACTAATCTTGAAGCTGGTCAAGCTTACTGCTTCAGAGTCCTTGCTGAAAATATATATGGAATTGGGGAAGGTTGTGAGACAGCTGGGCCAGTCAAAGCCTCAGGTGGGACTTCTTTAATAATGTTATAATTTAGCTAAACGTTTAAATATGCATATAGCCATATTCTAACTTTGATGTCTATTGCAGAACAACCTGGACCAGTTGCAGAATTTAAATCAATGGAGATCACCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9067
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 5830 | 17628 | 53 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 19556 | 31319 | 193 | 230 |
ENSDART00000126871 | Nonsense | 8851 | 22089 | 95 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 5830 | 17628 | 53 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 19556 | 31319 | 193 | 230 |
ENSDART00000126871 | Nonsense | 8851 | 22089 | 95 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44014033)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43139203 |
GRCz11 | 9 | 42940990 |
KASP Assay ID:
2260-2380.1 (used for ordering genotyping assays)
KASP Sequence:
CGTTTAAATATGCATATAGCCATATTCTAACTTTGATGTCWATTRCAGAA[C/T]AACCTGGACCAGTTGCAGAATTTAAATCAATRGAGATCACCAAGAATTCC
Long Flanking Sequence:
GTAGTGGTACCAAGTCATACACCATTGTTGTCAAAGTACTAGGTAAGACTCTCTTCTCTTAAAAAACATGCCATTTGAGTTTTAATCTTTGCTGTACCTAACTGTATTCAATAATGTGCACAGACACACCTGGACCTCCAGTCAATCTGATTGTTAAGGAGACCTCAAAGGACCATGTATCCATTACTTGGGATGCTCCATTAATTGATGGTGGAAGTCCAGTGAAGAGCTATGTGGTTGAAAAACGTCTGGCTGAGAGAAAGGCATGGACTTGTGTTGCTCCTGAGTGTCCCAAGACATCTTTTAGGATTACTAATCTTGAAGCTGGTCAAGCTTACTGCTTCAGAGTCCTTGCTGAAAATATATATGGAATTGGGGAAGGTTGTGAGACAGCTGGGCCAGTCAAAGCCTCAGGTGGGACTTCTTTAATAATGTTATAATTTAGCTAAACGTTTAAATATGCATATAGCCATATTCTAACTTTGATGTCTATTGCAGAA[C/T]AACCTGGACCAGTTGCAGAATTTAAATCAATGGAGATCACCAAGAATTCCTGCACTCTTGGCTGGAAGAAACCAATTAGTGATGGTGGAAGCCATGTTGTTGCATATGCTTTAGAGATCTGTGAAGGGGAGGACAAATGGAAGTTGCTAATGAAGTCTAAGGTCACACAGTACACAATTGGTGATCTAGTAGAAGGAAAGGAGTACAGCTTCAGGGTCAAGGCCATTAATGAATCAGCTGAAGGACCCCCGACTGAGCTCACTATCTTGGCTAAAGATCAAATAGGTATTCATATAGTCTCCCGCAGATGTTTTCAAAATGCTTTTCATTTTCTGATTCACTTACATTTTTATCATCACTTTAACATGTCATTGTAAGCAATTCTATATTCAATGATTACATTTATATAACATGATATTAAGCATTCCATTCCAAGTTTCCATGAATTGTTTCTACAATAACTCTATGCTCTGTTTACCTTGATAATACCTGGTCTACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18964
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 5830 | 17628 | 53 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 19556 | 31319 | 193 | 230 |
ENSDART00000126871 | Nonsense | 8851 | 22089 | 95 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 5830 | 17628 | 53 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 19556 | 31319 | 193 | 230 |
ENSDART00000126871 | Nonsense | 8851 | 22089 | 95 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44014033)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43139203 |
GRCz11 | 9 | 42940990 |
KASP Assay ID:
2260-2380.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTTTAAATATGCATATAGCCATATTCTAACTTTGATGTCTATTGCAGAA[C/T]AACCTGGACCAGTTGCAGAATTTAAATCAATGGAGATCACCAAGAATTCC
Long Flanking Sequence:
GTAGTGGTACCAAGTCATACACCATTGTTGTCAAAGTACTAGGTAAGACTCTCTTCTCTTAAAAAACATGCCATTTGAGTTTTAATCTTTGCTGTACCTAACTGTATTCAATAATGTGCACAGACACACCTGGACCTCCAGTCAATCTGATTGTTAAGGAGACCTCAAAGGACCATGTATCCATTACTTGGGATGCTCCATTAATTGATGGTGGAAGTCCAGTGAAGAGCTATGTGGTTGAAAAACGTCTGGCTGAGAGAAAGGCATGGACTTGTGTTGCTCCTGAGTGTCCCAAGACATCTTTTAGGATTACTAATCTTGAAGCTGGTCAAGCTTACTGCTTCAGAGTCCTTGCTGAAAATATATATGGAATTGGGGAAGGTTGTGAGACAGCTGGGCCAGTCAAAGCCTCAGGTGGGACTTCTTTAATAATGTTATAATTTAGCTAAACGTTTAAATATGCATATAGCCATATTCTAACTTTGATGTCTATTGCAGAA[C/T]AACCTGGACCAGTTGCAGAATTTAAATCAATGGAGATCACCAAGAATTCCTGCACTCTTGGCTGGAAGAAACCAATTAGTGATGGTGGAAGCCATGTTGTTGCATATGCTTTAGAGATCTGTGAAGGGGAGGACAAATGGAAGTTGCTAATGAAGTCTAAGGTCACACAGTACACAATTGGTGATCTAGTAGAAGGAAAGGAGTACAGCTTCAGGGTCAAGGCCATTAATGAATCAGCTGAAGGACCCCCGACTGAGCTCACTATCTTGGCTAAAGATCAAATAGGTATTCATATAGTCTCCCGCAGATGTTTTCAAAATGCTTTTCATTTTCTGATTCACTTACATTTTTATCATCACTTTAACATGTCATTGTAAGCAATTCTATATTCAATGATTACATTTATATAACATGATATTAAGCATTCCATTCCAAGTTTCCATGAATTGTTTCTACAATAACTCTATGCTCTGTTTACCTTGATAATACCTGGTCTACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11772
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 6674 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 20365 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 9695 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44010345)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43135515 |
GRCz11 | 9 | 42937302 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATAAAAAGGAAGGTGATGATGACTGGGTTCAAGACACAACTATTCCCT[T/A]GAGAAWAACAGAATTTGTGGTATCAAATCTACAGTCAGGAGGAAAATATC
Long Flanking Sequence:
TTAGAGGCTATATTGTTGAGAGAAAAGAGAGAAGAGGAATGAGATGGGTCAGAGCTTCAAAGAAGACTGTTTCTGATCTACGTTTTAAGGTCTCAGGCTTGTCAGAGGAAATTGAATATGAATTCAGAGTGACTGCAGAGAATAAAGCTGGTTTTGGTGAACCCAGTGAGCCATCACAACCTGTAATGACAAAGGATATTGCATGTAAGATGATCATTGCCAACATTTCCAGATAGTAATTCACACACATTTTTGTTTGAAAATTTTTAGCTACTCATTATTTTCTGTTACATTTTATATTTAGATAACAGTATTATTTGATTGTTTTTCAGATCCACCAGGGCCTCCATCAAACCCACGGATTACTGACACCACTAAAACAACAGCAACATTTAACTGGGGTAGACCCTTTTATGATGGTGGACTTGATGTGACAGGATACATTGTTGAGCATAAAAAGGAAGGTGATGATGACTGGGTTCAAGACACAACTATTCCCT[T/A]GAGAATAACAGAATTTGTGGTATCAAATCTACAGTCAGGAGGAAAATATCACTTCAGAGTCAGTGCGCTTAATTCTGAAGGGCTTGGTGAACCATCTGAAGTAGAGCAAGTTGTTGAACTGGTGGATCGAGAGGAGGTTCCTGACTTTGAGCTTGATGCAGAGCTGAGAAAAACACTTGTTGTGAAGTCGGGTGCTTCAATCCGTATATTTGTGCCAATTAAGGGCCGGCCAGCTCCTGAAGTAGTATGGTATAAGGAAAATGTACCTCTTAAAGGGCGTGCTCACATTGATACTACGGAATCATACACTTTAGTAGTCATCCCGGAATGTACACGATATGATGCAGGTAAATATGTCTTAACATTAGAAAATGTTGCTGGAAAGAAGACAGGATTTGTCAATGTCCGTGTTGTGGACACCCCAGGACCTCCAGTAAATTTAAAACCAAGAGAAATCACAAAGCATAGCATTACTCTCCAGTGGGAAATTCCTCTTATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41529
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 6884 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 20575 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 9905 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44009714)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43134884 |
GRCz11 | 9 | 42936671 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCAGAAATGCTCATACAAGATTCCAGACTTAGAAGAGGCTGCTGAATA[T/A]TACTTTAGAGTTTCAGCTGAAAATGAAATGGGCATCGGTGAACCAGCAGA
Long Flanking Sequence:
GAGGAGGTTCCTGACTTTGAGCTTGATGCAGAGCTGAGAAAAACACTTGTTGTGAAGTCGGGTGCTTCAATCCGTATATTTGTGCCAATTAAGGGCCGGCCAGCTCCTGAAGTAGTATGGTATAAGGAAAATGTACCTCTTAAAGGGCGTGCTCACATTGATACTACGGAATCATACACTTTAGTAGTCATCCCGGAATGTACACGATATGATGCAGGTAAATATGTCTTAACATTAGAAAATGTTGCTGGAAAGAAGACAGGATTTGTCAATGTCCGTGTTGTGGACACCCCAGGACCTCCAGTAAATTTAAAACCAAGAGAAATCACAAAGCATAGCATTACTCTCCAGTGGGAAATTCCTCTTATTGATGGTGGCTCAAAGATAAAAAATTATATTATTGAGAAGCGTGAGGCAACGCGAAAAGCCTACTCAGTTATCACAACAAACTGGCAGAAATGCTCATACAAGATTCCAGACTTAGAAGAGGCTGCTGAATA[T/A]TACTTTAGAGTTTCAGCTGAAAATGAAATGGGCATCGGTGAACCAGCAGAGACACCTGATCCAATAAGAGCTTCCCAGGCTCCTTCTGCACCAGATGATCTTATTGTCACTGATGTTTCCAAGGACACTGCAACTCTTGCATGGACAAAACCTAAACATGATGGTGGTAGTCGAATCACTGGGTATGTAATTGAGGCTCAACTGAAAGACTCTGATCAATGGGCCCATGTGACAACAATAAAAGCTTTGGACTACATTGCAACAGAATTGGTGGAAAATGCAGAATATGTGTTCCGCATATTTGCTGTAAATAGCTCAGGCAGAAGTGAACCTCGAGAAAGTCGACCAGTTGTAATAAAGGAGCAAACCACAGCTCCAGAATTTGACCTCAGAAGTATATATCAAAAGACAGTGGTAGCTAAAGCAGGTGATAATCTTAAAGTTGAGATCCCTGTTCTTGGTCGTCCTAGACCACTTGTTGTATGGAAGAAAGAAGATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16825
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 7599 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 21290 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 10620 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44007569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43132739 |
GRCz11 | 9 | 42934526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGTGGGAGAACCTCTTGAATCTGAACCTGCTGTTGCTACTAATCCGTA[T/A]GTGCCATCTGATCCTCCACAGGCACCAGAAGTAACTGCTATCACAAAGGA
Long Flanking Sequence:
ACAGGCCGACCAATACCTTCCATAGTTTGGACAAAAGATGGCAAGGAACTCGAGGACACTGCAAAAATGGAGATCAAAACATTAGATTTCTACAGTTGTTTGATCAACAAAGATTCTTTGCGTAGAGATGGTGGTGCATACACTCTAACTGCTAGCAATCCTGGAGGATTTGCTAAATTTGTCTTCAATGTTAAAGTTCTTGACAGACCTGGTCCTCCTGAGGGCCCATTGCATGTCACAGACATGACAGTAGAGAAATGCGTTCTGTCATGGCTACCACCACTTCATGATGGAGGAGGAAAGATTGAATATTACATCATTCAAAGACGTGAAACAAGTAGACTTACATGGACAAATGTAGCTACAGATTTACAAGTAAACCGCTATAAAGTTACCAAATTGCTGAAGGGAAATGAATATATCTTCAGAGTCATGGCTGTGAACAAGTATGGAGTGGGAGAACCTCTTGAATCTGAACCTGCTGTTGCTACTAATCCGTA[T/A]GTGCCATCTGATCCTCCACAGGCACCAGAAGTAACTGCTATCACAAAGGATTCAATGGTGGTATGTTGGGGACATCCTGAGTACAATGGTGGAAGTAGCATTAATACCTACATCATTGAGAGGAGAGATAAAACTGGTCTTCGTTGGGTAAAATGCAACAAAAGGACTGTTACTGATCTGCGCTTCAAAGTGTCAGGATTAACACCTGGACATGAGTATGAATACAGAATCCTAGCTGAAAATGCTGCTGGCTTAAGTGCTCCAAGCCCTTCAAGTCCATTCTACAAAGCCTGTGACACGATATTCCAACCTGGACCACCTGGAAACCCCAGGGTTTTGGATACAACTAAATCATCTATTACTATTGCTTGGAATAAACCAGTTTATGATGGTGGCTCAGATATTACAGGCTATATTGTTGAGACATGCCTCCCAGAGGAAGATGAATGGACAATTGTTACCCCAATGGCGGGACTGACAGCAACATCATTCACCATAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13049
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 7952 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 21643 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 10973 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44006510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43131680 |
GRCz11 | 9 | 42933467 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAAACGTGAAWCTACAAGAAAAGCATATTCCATTGTCAATGCCTCTTG[T/A]CCTAAAACAAGTTGGAGAATTGGAGATTTACAAGAAGGAAATTTGTATTT
Long Flanking Sequence:
GTTGGAGAGCCAGCTTCTGTGCCTGGTTCGCCTAAAGCAGAGGACAGACTCCTTCCACCTGAAATTGAGCTTGACTCAGACCTTCGCAAAGTTGTGAACATCAGAGCATGCAGTACCTTAAGATTATTTGTACCAGTTAAAGGAAGACCTGCGCCAGAAATCAGATGGTCAAGGGAGAAAGGAGAACCCCTTGATAGAGCATCCATTGAAATTACACCTTCTTTTACCACACTGCTCATTGAAAATGTAGATAGATTTGATGGTGGAAAATATATGTTAACAGTGGAAAACAGTTCAGGAACAAAAACAGCATTTATCAATGTCCGAGTTCTTGACACTCCTGGTGCACCACAAAACCTTACCATCAAAGAAATCACAAAAGATTCTGTTTCACTCATCTGGGACCCTCCAGTCATTGATGGTGGATCAAGAATCAGGCATTACATTGTGGAAAAACGTGAATCTACAAGAAAAGCATATTCCATTGTCAATGCCTCTTG[T/A]CCTAAAACAAGTTGGAGAATTGGAGATTTACAAGAAGGAAATTTGTATTTCTTCAGAATTTTGGCAGAAAATGAGTATGGTGTAGGTCTTCCAGTAGAGACAATGGAAGCTATAAAAATCTCTGAGAGACCTCTTCCTCCAGGAAAAGTTACTCTAAAAGAAGTAACTAGCAACAGTGTTACACTTTCTTGGGAGAAGCCAGACCATGATGGAGGAAGCAGAATTACCGGTTATATTGTTGAAATGCAAGGAAAAAACAGTGACAAATGGACCCAGGTAATGACTGTTAAAGTAACAGAAGCAGTTGTTGTTGGCCTTACACAAGGTGAAGAATACTCCTTCCGCATTTCTGCAACCAATGAAAAAGGAATAAGTGATCCGCGTCCACTTAGCGTCCCTGTCATTGCTAAGGATGTTGTTATTGCCCCTGCCTTCAAACTGTTATTTAGCACATTCAGTGTTCTGGCAGGTGATGATCTGAAAATTGACGTGCCTTATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41528
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 7985 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 21676 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 11006 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44006413)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43131583 |
GRCz11 | 9 | 42933370 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCTTCAGAATTTTGGCAGAAAATGAGTATGGTGTAGGTCTTCCAGTA[G/T]AGACAATGGAAGCTATAAAAATCTCTGAGAGACCTCTTCCTCCAGGAAAA
Long Flanking Sequence:
ACATCAGAGCATGCAGTACCTTAAGATTATTTGTACCAGTTAAAGGAAGACCTGCGCCAGAAATCAGATGGTCAAGGGAGAAAGGAGAACCCCTTGATAGAGCATCCATTGAAATTACACCTTCTTTTACCACACTGCTCATTGAAAATGTAGATAGATTTGATGGTGGAAAATATATGTTAACAGTGGAAAACAGTTCAGGAACAAAAACAGCATTTATCAATGTCCGAGTTCTTGACACTCCTGGTGCACCACAAAACCTTACCATCAAAGAAATCACAAAAGATTCTGTTTCACTCATCTGGGACCCTCCAGTCATTGATGGTGGATCAAGAATCAGGCATTACATTGTGGAAAAACGTGAATCTACAAGAAAAGCATATTCCATTGTCAATGCCTCTTGTCCTAAAACAAGTTGGAGAATTGGAGATTTACAAGAAGGAAATTTGTATTTCTTCAGAATTTTGGCAGAAAATGAGTATGGTGTAGGTCTTCCAGTA[G/T]AGACAATGGAAGCTATAAAAATCTCTGAGAGACCTCTTCCTCCAGGAAAAGTTACTCTAAAAGAAGTAACTAGCAACAGTGTTACACTTTCTTGGGAGAAGCCAGACCATGATGGAGGAAGCAGAATTACCGGTTATATTGTTGAAATGCAAGGAAAAAACAGTGACAAATGGACCCAGGTAATGACTGTTAAAGTAACAGAAGCAGTTGTTGTTGGCCTTACACAAGGTGAAGAATACTCCTTCCGCATTTCTGCAACCAATGAAAAAGGAATAAGTGATCCGCGTCCACTTAGCGTCCCTGTCATTGCTAAGGATGTTGTTATTGCCCCTGCCTTCAAACTGTTATTTAGCACATTCAGTGTTCTGGCAGGTGATGATCTGAAAATTGACGTGCCTTATGTTGCTCAGCCCAAGGCAGCAGTTGTTTGGCAAAAAGATGGCATTTCTTTGAAGGAGACAACAAGAGTAAATACTGAAGTAGCAGAGAGACATCTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16217
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 8346 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 22037 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 11367 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44005330)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43130500 |
GRCz11 | 9 | 42932287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAACAGCTTGCTGTGGGTGAAACAAAACAAAACAATCATTCCAGAMACA[C/T]GATTCAAGATAGGTGGTCTTGAAGAAGGCATTGAATATGAATTTAGAGTG
Long Flanking Sequence:
ACATCAATGTTATTGTACTTGATAAACCTGGACCACCAACTGGCCCAATCAAAATAGAGGAGGTAACTGCAGACAGTGTTACATTGTCATGGCAGCCTCCAGAGTATGAAGGAGGATGCAGCATTAATAACTACATTGTTGAAAAGCGAGACACATCCACCACAAATTGGCAGATTGTTTCTGCAACAGTGGCAAGAACAACAACTAAAGCGGCAAGACTCAAGACTGGCTGTGAGTATCAATTTAGGATTGCTGCGGAAAACAGATATGGAAAGAGTTCAGTTATTGTGTCTGAGCATGTTGTGGCGCAGTATCCCTTTGAAATTCCACATCCACCCGGAATTCCAGCTGTTCAGTCTGCTACTAAAGAAAGCATGGTTGTTGTATGGAACAAACCCAGCAGTGATGGTGGAAGCAAGATTTTGGGATATCACATTGAAAGTAAAGAAAAAAACAGCTTGCTGTGGGTGAAACAAAACAAAACAATCATTCCAGACACA[C/T]GATTCAAGATAGGTGGTCTTGAAGAAGGCATTGAATATGAATTTAGAGTGTATGCTGAGAATATAGTTGGTCTAAGCAAAGCAAGCAAAGTGTCTGAAATTCAAGTGGCTAGAGATCCATGTGATCCTCCAGGCAAACCTGAAGCAGTTATCGTGAAAAGAAGCTCTGTAACACTCAGGTGGACACCCCCACAGTTTGATGGTGGAATCAAAATTACTGGATATGTTGTTGAAAAGAAAGAACTGCCTAATGGTCGATGGATGAAAGCCTCTTTTGCTAACATTATTGAGACTGAATTTGTTGTCAGTGGGTTGGTAGAGGAGCAACAATATGAGTTCCGTGTCATTGCAAGAAATGCTGCAGGTGTCTCTAGTGTTCCATCAGACAGCACTGGTGCAATAACAGCAAAGGATGAAGTTGATCCACCCCAAATTGACTTGGATGCCAAATACTCTCAAAATGTTGTTGTTAATGCTGGTGAATCATTCAGAATTGATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45374
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 8636 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 22327 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 11657 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44004459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43129629 |
GRCz11 | 9 | 42931416 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTGTGGAAAGAAGAGAAACCAGTCGATTGGTTTGGACTGTTGTAGAAT[T/A]AAAGGTACAAACCCTTAATCTCAAAATTACAAAACTTCTTCCTGGAAATG
Long Flanking Sequence:
TAGTGTTCCATCAGACAGCACTGGTGCAATAACAGCAAAGGATGAAGTTGATCCACCCCAAATTGACTTGGATGCCAAATACTCTCAAAATGTTGTTGTTAATGCTGGTGAATCATTCAGAATTGATGCAGGGATACTTGGCAAACCTATTCCTTCAGTGCACTGGATAAAATCTGGCGAAGAACTTACAAATACTGCAAGGCTTGAAATCAAGAATACTGACTTCACGACAACTTTAAGTGTCAAGGAGGCTATCCGTGTTGATGGAGGCCAGTATACATTATTACTGAAAAATGTTGGTGGAGAGAAATCAGTAATCATCAATGTCAAGGTTCTGGACAGGCCTGGGCCTCCAGATGGTCCAATTTCAATCTATGGAGTTACAAGTGAAAAGTGTTGCATTTCCTGGAAAACTCCATTGCATGATGGAGGTGCAGAGGTGTCTCATTACATTGTGGAAAGAAGAGAAACCAGTCGATTGGTTTGGACTGTTGTAGAAT[T/A]AAAGGTACAAACCCTTAATCTCAAAATTACAAAACTTCTTCCTGGAAATGAGTATATTTTTAGAGTAATACCTGTGAACAAATATGGAATTGGTGAGCCTTTGGAATCTGATCCAGTGATTGCAGCAAATCCGTTTGTCACACCTGAAGCACCAAGTAATGTTGAAGTGTCAAACATAACAAAGGATTCCATGGTTATCACATGGGAAAGACCCACTAATGATGGTGGCAGTGCAATTACGGGATATATTGTTGAAAAAAGAGACAAAGAAGGTGTTAGGTGGACAAGGTGCAACAAACGTGTAGTGAGTGAACTACGATTTAGAGTAACAGGACTTCTTGAAATGAGAAGTTATGAATTCCGTGTGTCTGCTGAAAACGCAGCTGGAGTTGGTAAGCCAAGTCCACCCACAGTGTACTTCAAAGCAGCGGATCCAGTCTTTAAGCCTGGCCCACCCAACAACCCTAAAGTAGCTTATGTGTCAAGAGCATCTGTTGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34741
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 8795 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 22486 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 11816 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44003981)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43129151 |
GRCz11 | 9 | 42930938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGATCCAGTCTTTAAGCCTGGCCCACCCAACAACCCTAAAGTAGCTTA[T/A]GTGTCAAGAGCATCTGTTGTACTGCATTGGAGCAAGCCAATTTACGATGG
Long Flanking Sequence:
TTGGTTTGGACTGTTGTAGAATTAAAGGTACAAACCCTTAATCTCAAAATTACAAAACTTCTTCCTGGAAATGAGTATATTTTTAGAGTAATACCTGTGAACAAATATGGAATTGGTGAGCCTTTGGAATCTGATCCAGTGATTGCAGCAAATCCGTTTGTCACACCTGAAGCACCAAGTAATGTTGAAGTGTCAAACATAACAAAGGATTCCATGGTTATCACATGGGAAAGACCCACTAATGATGGTGGCAGTGCAATTACGGGATATATTGTTGAAAAAAGAGACAAAGAAGGTGTTAGGTGGACAAGGTGCAACAAACGTGTAGTGAGTGAACTACGATTTAGAGTAACAGGACTTCTTGAAATGAGAAGTTATGAATTCCGTGTGTCTGCTGAAAACGCAGCTGGAGTTGGTAAGCCAAGTCCACCCACAGTGTACTTCAAAGCAGCGGATCCAGTCTTTAAGCCTGGCCCACCCAACAACCCTAAAGTAGCTTA[T/A]GTGTCAAGAGCATCTGTTGTACTGCATTGGAGCAAGCCAATTTACGATGGTGGCTGTGAGATTCAAAGTTATATTGTTGAGGCATGTGAAGTCACTTCAGATGAATGGGTGATGTGTACACCACCATCAGGAATAACTGAAACAAGATTTGAAGCTAAAAAACTGCTTGAAAAGCATGAGTACAAATTCCGAATTTGTGCTGTTAATAAGATTGGCGTCGGAGAAACTGCTGATATCCCAGGATCTGTTATCATTGAGGATAAACTTGAGGCACCAGATATTGATCTTGATGCTGACCTGAGAAAGATGATCACTGTCAGAGCTGGAGGTTCTCTTAGATTGTTTGTTCCTATCCGGGGACGACCAACTCCTGAAGTCAAATGGGGAAAAACTGAAGGTGAAATCAATGAGGCAGCACAGATTGATATTACAAGCAGTTTTACCTCACTTGTAATTGAAAATGTTAACAGGTTTGACAGTGGAAAATACACTTTGACCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41527
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 8819 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 22510 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 11840 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44003909)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43129079 |
GRCz11 | 9 | 42930866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCATTGGAGCAAGCCAATTTACGATGGTGGCTGTGAGATTCAAAGTTA[T/A]ATTGTTGAGGCATGTGAAGTCACTTCAGATGAATGGGTGATGTGTACACC
Long Flanking Sequence:
GAGTATATTTTTAGAGTAATACCTGTGAACAAATATGGAATTGGTGAGCCTTTGGAATCTGATCCAGTGATTGCAGCAAATCCGTTTGTCACACCTGAAGCACCAAGTAATGTTGAAGTGTCAAACATAACAAAGGATTCCATGGTTATCACATGGGAAAGACCCACTAATGATGGTGGCAGTGCAATTACGGGATATATTGTTGAAAAAAGAGACAAAGAAGGTGTTAGGTGGACAAGGTGCAACAAACGTGTAGTGAGTGAACTACGATTTAGAGTAACAGGACTTCTTGAAATGAGAAGTTATGAATTCCGTGTGTCTGCTGAAAACGCAGCTGGAGTTGGTAAGCCAAGTCCACCCACAGTGTACTTCAAAGCAGCGGATCCAGTCTTTAAGCCTGGCCCACCCAACAACCCTAAAGTAGCTTATGTGTCAAGAGCATCTGTTGTACTGCATTGGAGCAAGCCAATTTACGATGGTGGCTGTGAGATTCAAAGTTA[T/A]ATTGTTGAGGCATGTGAAGTCACTTCAGATGAATGGGTGATGTGTACACCACCATCAGGAATAACTGAAACAAGATTTGAAGCTAAAAAACTGCTTGAAAAGCATGAGTACAAATTCCGAATTTGTGCTGTTAATAAGATTGGCGTCGGAGAAACTGCTGATATCCCAGGATCTGTTATCATTGAGGATAAACTTGAGGCACCAGATATTGATCTTGATGCTGACCTGAGAAAGATGATCACTGTCAGAGCTGGAGGTTCTCTTAGATTGTTTGTTCCTATCCGGGGACGACCAACTCCTGAAGTCAAATGGGGAAAAACTGAAGGTGAAATCAATGAGGCAGCACAGATTGATATTACAAGCAGTTTTACCTCACTTGTAATTGAAAATGTTAACAGGTTTGACAGTGGAAAATACACTTTGACCCTGGAAAATGCTAGTGGAACAAAATCTGCATTTATTAGCGTCAGAGTATTAGATACTCCTGATATGCCTGCGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13884
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 8935 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 22626 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 11956 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 8935 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 22626 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 11956 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44003563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43128733 |
GRCz11 | 9 | 42930520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCTGAAGTCAAATGGGGAAAAACTGAAGGTGAAATCAATGAGRCAGCA[C/T]AGATTGATATTACAAGCAGTTTTACCTCACTTGTAATTGAAAATGTTAAC
Long Flanking Sequence:
AGCCAAGTCCACCCACAGTGTACTTCAAAGCAGCGGATCCAGTCTTTAAGCCTGGCCCACCCAACAACCCTAAAGTAGCTTATGTGTCAAGAGCATCTGTTGTACTGCATTGGAGCAAGCCAATTTACGATGGTGGCTGTGAGATTCAAAGTTATATTGTTGAGGCATGTGAAGTCACTTCAGATGAATGGGTGATGTGTACACCACCATCAGGAATAACTGAAACAAGATTTGAAGCTAAAAAACTGCTTGAAAAGCATGAGTACAAATTCCGAATTTGTGCTGTTAATAAGATTGGCGTCGGAGAAACTGCTGATATCCCAGGATCTGTTATCATTGAGGATAAACTTGAGGCACCAGATATTGATCTTGATGCTGACCTGAGAAAGATGATCACTGTCAGAGCTGGAGGTTCTCTTAGATTGTTTGTTCCTATCCGGGGACGACCAACTCCTGAAGTCAAATGGGGAAAAACTGAAGGTGAAATCAATGAGGCAGCA[C/T]AGATTGATATTACAAGCAGTTTTACCTCACTTGTAATTGAAAATGTTAACAGGTTTGACAGTGGAAAATACACTTTGACCCTGGAAAATGCTAGTGGAACAAAATCTGCATTTATTAGCGTCAGAGTATTAGATACTCCTGATATGCCTGCGAACTTCCGTGTGAAGGAAATAACAAAGAACTCGGTTACTCTTACCTGGGAGCCTCCTTTGCTGGATGGTGGTGCTAAAATAAAAAGCTACATTGTTGAAAAACGAGAGAGTACACGAAAGGTATATTCTGCTGTTACTACTTGCAACAAGATGACATGGAAAATTGAACCACTTGAAGAGGGAAGTATCTACTTCTTCAGAGTTCTTGCTGAAAATGAGCATGGCATTGGATTGCCCGCAGAGACTCCAGAACCACTGAAAATTTCAGAGGTGCCACAACCCCCTGGCAAAGTTTCTGTAGTGGATGTAACACGGAAGAGTGTTTCTCTAAAATGGGAAAAGCCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12872
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 8935 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 22626 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 11956 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 8935 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 22626 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 11956 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 44003563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43128733 |
GRCz11 | 9 | 42930520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCTGAAGTCAAATGGGGAAAAACTGAAGGTGAAATCAATGAGRCAGCA[C/T]AGATTGATATTACAAGCAGTTTTACCTCACTTGTAATTGAAAATGTTAAC
Long Flanking Sequence:
AGCCAAGTCCACCCACAGTGTACTTCAAAGCAGCGGATCCAGTCTTTAAGCCTGGCCCACCCAACAACCCTAAAGTAGCTTATGTGTCAAGAGCATCTGTTGTACTGCATTGGAGCAAGCCAATTTACGATGGTGGCTGTGAGATTCAAAGTTATATTGTTGAGGCATGTGAAGTCACTTCAGATGAATGGGTGATGTGTACACCACCATCAGGAATAACTGAAACAAGATTTGAAGCTAAAAAACTGCTTGAAAAGCATGAGTACAAATTCCGAATTTGTGCTGTTAATAAGATTGGCGTCGGAGAAACTGCTGATATCCCAGGATCTGTTATCATTGAGGATAAACTTGAGGCACCAGATATTGATCTTGATGCTGACCTGAGAAAGATGATCACTGTCAGAGCTGGAGGTTCTCTTAGATTGTTTGTTCCTATCCGGGGACGACCAACTCCTGAAGTCAAATGGGGAAAAACTGAAGGTGAAATCAATGAGGCAGCA[C/T]AGATTGATATTACAAGCAGTTTTACCTCACTTGTAATTGAAAATGTTAACAGGTTTGACAGTGGAAAATACACTTTGACCCTGGAAAATGCTAGTGGAACAAAATCTGCATTTATTAGCGTCAGAGTATTAGATACTCCTGATATGCCTGCGAACTTCCGTGTGAAGGAAATAACAAAGAACTCGGTTACTCTTACCTGGGAGCCTCCTTTGCTGGATGGTGGTGCTAAAATAAAAAGCTACATTGTTGAAAAACGAGAGAGTACACGAAAGGTATATTCTGCTGTTACTACTTGCAACAAGATGACATGGAAAATTGAACCACTTGAAGAGGGAAGTATCTACTTCTTCAGAGTTCTTGCTGAAAATGAGCATGGCATTGGATTGCCCGCAGAGACTCCAGAACCACTGAAAATTTCAGAGGTGCCACAACCCCCTGGCAAAGTTTCTGTAGTGGATGTAACACGGAAGAGTGTTTCTCTAAAATGGGAAAAGCCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21573
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 10291 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 23982 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 13312 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43999493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43124663 |
GRCz11 | 9 | 42926450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAAAGTGGAAATACCATTTAAAGGGCGTCCAACTCCAAAGATTGGATG[G/A]ATGAAAGATGGACAAGCACTTAAAGAGACAACCAGATTAAATGTCTCAAG
Long Flanking Sequence:
CTGACAGAGGGTGGTATTTATTACTTCAGAGTCATGGCAGAAAATGAATTTGGAATTGGCCTGCCTGTAGAAACAGAAGAATCTGTTAAGACAGCAGACCCCCCTTTATCAGTTGGCAAGGTCACTTTGACTGATGTCACAAAAACCACAGCATCACTATCCTGGGATAAACCAGATCATGATGGTGGCAGCAGAATATTGGGTTATTACATTGAAATGCAGCCAAAAGGATCAGAGGAATGGATTGTTGCCACAGTCTGCAAAACATGTGAGGGTACAGTGGCTGGACTTAGTTCAGGACAAGAATATCTCTTAAGAGTTTTAGCTTACAATGAGAAGGGAAAAAGTGATCCCAGGCCATTAGCTTCTCCTGTCATTGCCAAAGATGTTACTATTGAACCAAGCTTCAAACTAACTTTCAACACATACAGTGTTCAATCTGGCGAAGATCTCAAAGTGGAAATACCATTTAAAGGGCGTCCAACTCCAAAGATTGGATG[G/A]ATGAAAGATGGACAAGCACTTAAAGAGACAACCAGATTAAATGTCTCAAGCACTGCAACGTCAACGGTTCTTAAAATTAAAGAAGCAAATAGAGAGGACTCTGGCAAGTACACAATCACAGCTACAAACAATATAGGTACAGTCACAGAAGAGGTTGCCATAATCATTCTTGATAAACCAGGTCCACCAACTGGACCAGTCAAAATCGATGAAGTAAGTGCCACCTATGTTGTCATTTCCTGGGAGCCACCAGTTTACACAGGAGGTTGTCAGATAAACAACTATGTAGTGGAAAAACGTGATACAACCACGACTAACTGGCAGACCGTTTCTGCAACAATTGCTCGAACCACAATCAAAATCTCAAAGCTGAAGACTGGTTCTGAATATCAGTTTAGAGTGTTTGCTGAGAACAGATATGGAAAGAGCGGATCAATAGATTCAACGCCAGTTGTGGTCAGTTATCCTTTCACTGAGCCTGCAGCTCCTGGTGCACCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45373
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 10386 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 24077 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 13407 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43999208)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43124378 |
GRCz11 | 9 | 42926165 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCCTGGGAGCCACCAGTTTACACAGGAGGTTGTCAGATAAACAACTA[T/A]GTAGTGGAAAAACGTGATACAACCACGACTAACTGGCAGACCGTTTCTGC
Long Flanking Sequence:
GGACTTAGTTCAGGACAAGAATATCTCTTAAGAGTTTTAGCTTACAATGAGAAGGGAAAAAGTGATCCCAGGCCATTAGCTTCTCCTGTCATTGCCAAAGATGTTACTATTGAACCAAGCTTCAAACTAACTTTCAACACATACAGTGTTCAATCTGGCGAAGATCTCAAAGTGGAAATACCATTTAAAGGGCGTCCAACTCCAAAGATTGGATGGATGAAAGATGGACAAGCACTTAAAGAGACAACCAGATTAAATGTCTCAAGCACTGCAACGTCAACGGTTCTTAAAATTAAAGAAGCAAATAGAGAGGACTCTGGCAAGTACACAATCACAGCTACAAACAATATAGGTACAGTCACAGAAGAGGTTGCCATAATCATTCTTGATAAACCAGGTCCACCAACTGGACCAGTCAAAATCGATGAAGTAAGTGCCACCTATGTTGTCATTTCCTGGGAGCCACCAGTTTACACAGGAGGTTGTCAGATAAACAACTA[T/A]GTAGTGGAAAAACGTGATACAACCACGACTAACTGGCAGACCGTTTCTGCAACAATTGCTCGAACCACAATCAAAATCTCAAAGCTGAAGACTGGTTCTGAATATCAGTTTAGAGTGTTTGCTGAGAACAGATATGGAAAGAGCGGATCAATAGATTCAACGCCAGTTGTGGTCAGTTATCCTTTCACTGAGCCTGCAGCTCCTGGTGCACCATTTGTTTCATCAGTCACAAAAGACCACATGACAATTGAATGGAAACCCCCCAGCAATAATGGAGGCAGCCCTATTATTGGATATCACCTGGAGCGTAAAGAAAAGAACAGCATCTTATGGACCAAACTTAACAAACTTCTTATCACTGACACTCGATTGAGAACAAATGGTCTGGAGGAGGGAATTGAATATGAATATAGGGTTTTTGCTGAAAATATTGCAGGAATCAGTCCATCAAGCAAAGTGTCAGAAAGTGTTGTTGCACGTGACCCATGTGATCCACCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa787
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 11255 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 24946 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 14276 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43996603)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43121773 |
GRCz11 | 9 | 42923560 |
KASP Assay ID:
554-0692.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCCCAAGCACCCTTACCACCTGGTAAAATTACAGTTATTGATGTAACT[C/T]GACACACTGTTACTTTGTCATGGGAAAAGCCAGATCATGATGGTGGCAGC
Long Flanking Sequence:
AAAAGGCAGATGGCACCTTACCAGAGCGTGCTCAAATTGAGGTTACAGGCTCTTACACTGGGCTTGTTATTGACAATGTTAACCGGTTTGACACTGGCAAGTATGTTTTAACACTTGAAAACAATATTGGCTCAAAATCTGCATTTGTTAATGTCAAAGTTCTTGACTCTCCAAGTGCTCCAGTCAACTTTGAAGTTAAGGATGTAAAGAGAGATTCTGTCCAGCTACAATGGGAGCCTCCACAAATTGATGGTGGAGCCAAGATAACCCATTACATTGTAGAAAAGCGTGAATCCAAGAGACTAGCATTCACATCTATAACAAACAACTGTGTCAGAAATTCAATCAGGGTTGATGATCTCCAAGAAGGAGGTCTTTACCACTTCCGTGTATTGGCTGTCAATGAACTTGGTGTTGGTTTGCCTGCAGAGACTACAGAGGCTGTCAAAATTTCCCAAGCACCCTTACCACCTGGTAAAATTACAGTTATTGATGTAACT[C/T]GACACACTGTTACTTTGTCATGGGAAAAGCCAGATCATGATGGTGGCAGCAAAATCACAGGCTATATGGTGGAAATGATGACTAAGGGATCAGATAAATGGACTGCATGTGTCACAATAAAGGCACTGGAAGCCACAATTGAAGGACTTACAACAGGAGAGGAATACAGCTTCAGAATTACAGCAATTAATGACAAAGGAAAGAGCGATCCTAAACCACTGGGAGCACCTGTTGTGGCAAGAGATATTACTATTGAACCCATTATTGATTTGATGTTCAATACCTACAGTGTAAAAGCTGGAGATGATCTCAAAATAGATGTTCCGTTCAGAGGCAGACCTTCTCCAGAGGTTACATGGAAGAAGGATGGTCACTCGCTAAAGCAAACAACCAGAGTTAATGTTTTGACATCAAAGACATTATCCAAGATCACCATCAAGGATGCTACACGAGAAGATGCTGGAAAATATGAAATTACTTTAACCAATACATTTGGGGTC
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
Stage | Entity | Quality | Tag |
---|---|---|---|
Hatching:Long-pec ZFS:0000033 |
eye ZFA:0000107 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
Hatching:Long-pec ZFS:0000033 |
head ZFA:0001114 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
Hatching:Long-pec ZFS:0000033 |
larval locomotory behavior GO:0008345 |
absent PATO:0000462 |
abnormal PATO:0000460 |
Hatching:Long-pec ZFS:0000033 |
skeletal muscle ZFA:0005277 |
quality PATO:0000001 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa14565
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 11350 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 25041 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 14371 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43996316)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43121486 |
GRCz11 | 9 | 42923273 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAAGAGATATTACTATTGAACCCATTATTGATTTGATGTTCAATACCTA[C/A]AGTGTAAAAGCTGGAGATGATCTCAAAATAGATGTTCCGTTCAGAGGCAG
Long Flanking Sequence:
CGTGAATCCAAGAGACTAGCATTCACATCTATAACAAACAACTGTGTCAGAAATTCAATCAGGGTTGATGATCTCCAAGAAGGAGGTCTTTACCACTTCCGTGTATTGGCTGTCAATGAACTTGGTGTTGGTTTGCCTGCAGAGACTACAGAGGCTGTCAAAATTTCCCAAGCACCCTTACCACCTGGTAAAATTACAGTTATTGATGTAACTCGACACACTGTTACTTTGTCATGGGAAAAGCCAGATCATGATGGTGGCAGCAAAATCACAGGCTATATGGTGGAAATGATGACTAAGGGATCAGATAAATGGACTGCATGTGTCACAATAAAGGCACTGGAAGCCACAATTGAAGGACTTACAACAGGAGAGGAATACAGCTTCAGAATTACAGCAATTAATGACAAAGGAAAGAGCGATCCTAAACCACTGGGAGCACCTGTTGTGGCAAGAGATATTACTATTGAACCCATTATTGATTTGATGTTCAATACCTA[C/A]AGTGTAAAAGCTGGAGATGATCTCAAAATAGATGTTCCGTTCAGAGGCAGACCTTCTCCAGAGGTTACATGGAAGAAGGATGGTCACTCGCTAAAGCAAACAACCAGAGTTAATGTTTTGACATCAAAGACATTATCCAAGATCACCATCAAGGATGCTACACGAGAAGATGCTGGAAAATATGAAATTACTTTAACCAATACATTTGGGGTCAAGTCTGCAGAAATATCGGTCATCGTTCTTGATAAACCAGGCCCACCAGGTGCAATCAAGGTAGAGGAAATAAGCGCTGATTTTATTTCACTTTCATGGGACCCTCCGATATATGATGGTGGCTGTCAAATTAATAATTATGTAGTTGAAAAAAGAGATACGACTACTACAGCATGGCAAATTGTTTCAGCAACAGTTGCAAGAACATCAATCAAAGTATCTCGTTTGACACAAGGAACAGAATATCAGTTCCGTATTGCAGCAGAGAATCGTTATGGTAAAAGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13739
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 11468 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 25159 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 14489 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43995962)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43121132 |
GRCz11 | 9 | 42922919 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTCATGGGACCCTCCGATRTATGATGGTGGCTGTCAAATTAATAATTA[T/A]GTAGTTGAAAAAAGAGATACGACTACTACAGCATGGCAAATTGTWTCAGC
Long Flanking Sequence:
GAAGGACTTACAACAGGAGAGGAATACAGCTTCAGAATTACAGCAATTAATGACAAAGGAAAGAGCGATCCTAAACCACTGGGAGCACCTGTTGTGGCAAGAGATATTACTATTGAACCCATTATTGATTTGATGTTCAATACCTACAGTGTAAAAGCTGGAGATGATCTCAAAATAGATGTTCCGTTCAGAGGCAGACCTTCTCCAGAGGTTACATGGAAGAAGGATGGTCACTCGCTAAAGCAAACAACCAGAGTTAATGTTTTGACATCAAAGACATTATCCAAGATCACCATCAAGGATGCTACACGAGAAGATGCTGGAAAATATGAAATTACTTTAACCAATACATTTGGGGTCAAGTCTGCAGAAATATCGGTCATCGTTCTTGATAAACCAGGCCCACCAGGTGCAATCAAGGTAGAGGAAATAAGCGCTGATTTTATTTCACTTTCATGGGACCCTCCGATATATGATGGTGGCTGTCAAATTAATAATTA[T/A]GTAGTTGAAAAAAGAGATACGACTACTACAGCATGGCAAATTGTTTCAGCAACAGTTGCAAGAACATCAATCAAAGTATCTCGTTTGACACAAGGAACAGAATATCAGTTCCGTATTGCAGCAGAGAATCGTTATGGTAAAAGCCATGCTATTGACTCAGCCCCAATTGTAGCACAATACCCCTTTACACCTCCAGGCCCTCCAACCAGTCTTCAGGTTTCTCATGCCACTAAATCAGGAATGTTAGTTACATGGAACAGACCAGCAAGTGATGGTGGGAGTCCTATTGTTGGATATCACATAGAGTGCAAAGATCAGAGCAGCATTCTTTGGACAAAGATGAACAGAGGACTTATAACAGAAACTCAGTTCAAAGTAACTGGCTTGGAAGAAGGCCTACAGTATCAGTATAGAGTATATGCAGAAAATATAGCTGGCATTGGACCATGCACAAAGGCATGTGATCCTGTTTCTGCCCGAGATCCATGTGCACCACCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34740
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 11593 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 25284 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 14614 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43995589)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43120759 |
GRCz11 | 9 | 42922546 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTCTTTGGACAAAGATGAACAGAGGACTTATAACAGAAACTCAGTTC[A/T]AAGTAACTGGCTTGGAAGAAGGCCTACAGTATCAGTATAGAGTATATGCA
Long Flanking Sequence:
TATCGGTCATCGTTCTTGATAAACCAGGCCCACCAGGTGCAATCAAGGTAGAGGAAATAAGCGCTGATTTTATTTCACTTTCATGGGACCCTCCGATATATGATGGTGGCTGTCAAATTAATAATTATGTAGTTGAAAAAAGAGATACGACTACTACAGCATGGCAAATTGTTTCAGCAACAGTTGCAAGAACATCAATCAAAGTATCTCGTTTGACACAAGGAACAGAATATCAGTTCCGTATTGCAGCAGAGAATCGTTATGGTAAAAGCCATGCTATTGACTCAGCCCCAATTGTAGCACAATACCCCTTTACACCTCCAGGCCCTCCAACCAGTCTTCAGGTTTCTCATGCCACTAAATCAGGAATGTTAGTTACATGGAACAGACCAGCAAGTGATGGTGGGAGTCCTATTGTTGGATATCACATAGAGTGCAAAGATCAGAGCAGCATTCTTTGGACAAAGATGAACAGAGGACTTATAACAGAAACTCAGTTC[A/T]AAGTAACTGGCTTGGAAGAAGGCCTACAGTATCAGTATAGAGTATATGCAGAAAATATAGCTGGCATTGGACCATGCACAAAGGCATGTGATCCTGTTTCTGCCCGAGATCCATGTGCACCACCCAGTCAGCCACGCGTTATGAACATCACAAGAACATCTGTTTCTCTTTCTTGGACAAAACCGGAGTTTGACGGTGGAGCTAAGGTTACTGGCTATATTGTTGAGCGTAGTGAACTTCCAGATGGACGTTGGTTAAAGTGTAATTTCACCAATCTTCAAGAAACATATTTTGATGTGACTGGTCTGATTGAAGATCAAAGATATGATTTCCGAATCATTGCTAAAAATGCAGCTGGCTTATTCAGTGAACCATCAGAAAGCACTGGACCTGTAACAGTAAAAGATGATGTTGATCCACCACGCATAACAATTGAGGACAAGCTAAGACAACTTGTTGTAATAAAAGCTGGTGAAATACTGAGAATTGATGCTGAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15087
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 11800 | 17628 | 60 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 25491 | 31319 | 199 | 230 |
ENSDART00000126871 | Nonsense | 14821 | 22089 | 102 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43994968)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43120138 |
GRCz11 | 9 | 42921925 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATTTCTTCAACACTTACTAGTACAACGCTAATTGTGAGAGATGCCATT[A/T]GACGTGATTCAGGACAGYATKTTCTAACGTTACAGAATGTTGCAGGCACC
Long Flanking Sequence:
CACCCAGTCAGCCACGCGTTATGAACATCACAAGAACATCTGTTTCTCTTTCTTGGACAAAACCGGAGTTTGACGGTGGAGCTAAGGTTACTGGCTATATTGTTGAGCGTAGTGAACTTCCAGATGGACGTTGGTTAAAGTGTAATTTCACCAATCTTCAAGAAACATATTTTGATGTGACTGGTCTGATTGAAGATCAAAGATATGATTTCCGAATCATTGCTAAAAATGCAGCTGGCTTATTCAGTGAACCATCAGAAAGCACTGGACCTGTAACAGTAAAAGATGATGTTGATCCACCACGCATAACAATTGAGGACAAGCTAAGACAACTTGTTGTAATAAAAGCTGGTGAAATACTGAGAATTGATGCTGAAATATCAGGACGTCCAATTCCTGTGATTTCATGGGCAAAGGATGGAAAAGAAATTGAAGCCAAGGCCAGATTTGAGATTTCTTCAACACTTACTAGTACAACGCTAATTGTGAGAGATGCCATT[A/T]GACGTGATTCAGGACAGTATGTTCTAACGTTACAGAATGTTGCAGGCACCAGATCTTTGGCAGTAAATTGTAAGGTCCTGGACAGGCCTGGTCCATCATCTGGACCATTGGATATAACTGGTTTGACTGCAGAAAAATGTACATTGACCTGGGGACCACCTCAGGAAAATGGAGGCGCTGAAATTCAACACTACATTGTTGAGAAACGTGAGACTAGCCGGCTTGCCTGGACTCTGGTCTATGCAGACATGAAGGCCACAACATGTAAAGTAACAAAATTGCTCAAAGGTAATGAGTATATATTTAGAGTTCGAGGAGTTAATAAGTATGGAACTGGTGAAGCTCTGGAGAGTGATCCAGCAAAGGCAATGGATCCGTTCACAGTCCCTGCTGCACCAACAGATGTTGAAGTCACAAGTGTTACAAGTGAAGCAATGACAATTTGCTGGGAAAGACCCATCTCTGATGGAGGCAGTAGTATTTCTGGTTATGTAATTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2493
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 12384 | 17628 | 61 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 26075 | 31319 | 200 | 230 |
ENSDART00000126871 | Nonsense | 15405 | 22089 | 103 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43993105)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43118275 |
GRCz11 | 9 | 42920062 |
KASP Assay ID:
554-2808.1 (used for ordering genotyping assays)
KASP Sequence:
GGATAAAGTGTGGTTCCACCAAATCCACTCATTTCGTTGTTGATGGTTTG[A/T]GAGAAAATGCTGAATACTACTTCAGAGTTCGTGCTGAAAACCATGCTGGG
Long Flanking Sequence:
CAGTCAAAAACTACCTTGTTGATCTCCGCGAGGCAACTAAGATGGGCTGGAGCAGGATTTCAAACAGTTGTCCCAGATTGACTTATAAAGTGACTAATCTACAAGAGGGGGGTGTATATTATTTCAGAGTTACTGGTGAGAATGAGTATGGCGTAGGAGTGCCACTTGAGACCAAGGAAGGAACAAAGATTACAGGTAAAATTAAATAATTATATTAACTGAGCCTTTACTACAGCACAAATATCTGTTGATTTCCTCAAACCTTTAATGAATATTTTTTTCCTCATATGCTACTTTTACTTTTAGAAAAACCAAGCCCACCACCCAAGCTTGGGGTAACTGATGTCACAAAAGAAAGTGTCTCACTAGCATGGCTTAAACCAGAACATGATGGAGGAAGCAGAATAACAAACTACCTGGTTGAGGCCCTTGAAAAAGGACAACAAAAGTGGATAAAGTGTGGTTCCACCAAATCCACTCATTTCGTTGTTGATGGTTTG[A/T]GAGAAAATGCTGAATACTACTTCAGAGTTCGTGCTGAAAACCATGCTGGGCTAAGCGACCCCAAAGACATGGTTTTACCTGTGCTTGTTAAAGACCAGCTGGGCAAGTTATTTATTATGGATTGTTTTTTATTTTTGAACATATGTAATATTTAAATACCACTTGTTGAATTATTATCTAATGCTGTTGCTTTCTGTAATCAACAGAGGCGCCAGAAATTAATATGAAGGACTTCCAACACAATACTGCCTATGTTAAGGCAGGTTCAAATCTCAAGATTGAGATCCCCCTTACTGGTAAACCTTTACCAAAAGTTTCCCTGTCTAAAGATGGACAGGTTCTAAAGTCTACCATGAGATTCAACTTTGATGTGACAACTGACTCCCTTATAATTTATTTGCGTGAGAGTGTTGCTTCAGATGCAGGCAGATATGATATCACAGCCTCTAACTCTAATGGAACCACAAAATCTTTTGTGAATGTTGTGGTTCTTGATAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21572
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Essential Splice Site | 13212 | 17628 | 67 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 26903 | 31319 | 206 | 230 |
ENSDART00000126871 | Essential Splice Site | 16233 | 22089 | 109 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43989872)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43115042 |
GRCz11 | 9 | 42916829 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGACGTTCGATTGAGATTGTGCAGCCAGTGCAGGCCAAAGATATTCTGG[G/A]TTTGTACTTTTTAACGGTCAAAATTATAAAATGTTTTACTGATTTTTCTT
Long Flanking Sequence:
CAGAAGGAAATGAATATCAGTATCGTGTCTGTGCAATCAACAAAGCTGGTGCAGGTCCATATTCTGATGTCTCCATCTTCTACAAAGCTTATGACCCAATTGGTATGTTTTTTTTTTCTCTAGACTGTTTTTAAGAATGTGAATATAAATGAGTATAATGTATGCAATCATAAACATATAAATTGCTGTTTTAGATCCACCAAGTGAGCCTACCAAGCTCAGAGTTGTTGATTCAACAAAGACATCAATTACTCTTGGATGGGTGAAGCCTGTTTATGATGGTGGGAGCGAAATCACAAGCTACGTTATTGAACAAAGAATAGCTGATGAGACAGAATGGGTCACTATAAGTTCTAAAGGAGAAGTAAGAACTACTGAGTTTGTTGTGTCCCATTTAAAACCTGGAGTTTACTACTACTACCGTGTCTCTGCTGTGAATTGTGTTGGAACTGGACGTTCGATTGAGATTGTGCAGCCAGTGCAGGCCAAAGATATTCTGG[G/A]TTTGTACTTTTTAACGGTCAAAATTATAAAATGTTTTACTGATTTTTCTTACAATAGCCTAATCAAATATGTTTCTTTTTCAATTTAACAGAGGAAGCTGATGTGGATCTTGACATCTCAATGTCAACTCAGTACATAGCTAAGGCTGGTAGAGATGTTGAAATTGTAATTCCTCTTAAGGGTAGACCTGCCCCAAATGTTACATGGCGAAAGGGAGACAAAAACATTAGTGGTGATGCAAGATATGCCATCAGAAACACAGAATACTCAACTACACTGATCATTCCAAAAGTCACAAGGGATGACACTGGCAAATATCTTCTTGAAATTGAAAATGGAGTTGGGGAGCCAAAAACCATCACAGTTTCTGTTAAAGTATTGGACACACCATCTGCCTGTAACAGGTTGATAGTGAAGAATGTGACAAGAGGTAAACTTACTCTAAGCTGGGAACCACCTTATATTGATGGTGGCTCTCCAATCACAAATTACGTTGTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12142
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 13580 | 17628 | 68 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 27271 | 31319 | 207 | 230 |
ENSDART00000126871 | Nonsense | 16601 | 22089 | 110 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43988678)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43113848 |
GRCz11 | 9 | 42915635 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGCWAGTCTCATTGTAAGAAATGCAAGAAAGGAAAATGCAGGAAAATA[C/A]ACYTTGGTACTTGATAACAAACTTGTCAAGAACTTCTTTGACATCAAAGT
Long Flanking Sequence:
GATCTTGTACTGGTGGACTCAACTAATACATCTGTATCACTGGCATGGACAAAGCCAGATCATGATGGTGGAAGTCACATTAATGAGTACATTATTGAGAAAAAAACAAAGGATGAAGAAACATGGAGCTCTGGTGGCACATGCAGACGTTGCCAGTGTGAAGTAACTGAACTTAAAGAGCTTTCTGAAGTTTACTTTAGAGTTTTTGCAAAAAATGAGAAGGGTCGCAGTGACTTCTCTCAAATCGGGCCAATCACTGTAAAGGAATTCCTTATACCTCCTGAGGCAAACCTTATTGATTATCCTAATGGAGAATTAAGTGTTCGCATTGGACAAAATGTGAATATTGACTTACCCTACAAAGGTAAACCCAAACCAATTATTCAGTGGATGAAAGACGATGTTATACTCAAGGAAAGTGAACAAGTTCGTTTCAGGCAAACAGAGAACAAGGCAAGTCTCATTGTAAGAAATGCAAGAAAGGAAAATGCAGGAAAATA[C/A]ACCTTGGTACTTGATAACAAACTTGTCAAGAACTTCTTTGACATCAAAGTCATTACACTTGGGCCACCATCTCAGCCCATAGGCCCAATCCGTTTTGATGAAATTAAAGCCCAGAGTATTATTATCTCATGGGATGTACCCCAAGAAGATGGCGGAGGAGAGATCACCTGCTACAGTGTAGAAAAGCGAGAGACATCTCAAGCAGCATGGAAGATAGTTTGCTCTAGTGTGGTCAGGACAACATTCAAGATACCAAATTTAGTTAAGGGTACAGAATACCAATTTAGGGTGCGTGCAGAGAACAAATATGGAGTAAGTGATCCTCTAACCTCACCAGATGTGGTCGCTCAACACCAATATAAGCCACCAGGTCCACCAGGAAAACCTGTAGTATTCAATGTTACAAGTGATGGCATGACTGTTCAGTGGGATGCCCCAGGTTTTGATGGTGGTTCTCCAATCACTGGATACCACCTTGAGAAGAAAGACAGGAACAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2492
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 13780 | 17628 | 68 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 27471 | 31319 | 207 | 230 |
ENSDART00000126871 | Nonsense | 16801 | 22089 | 110 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43988080)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43113250 |
GRCz11 | 9 | 42915037 |
KASP Assay ID:
554-2790.1 (used for ordering genotyping assays)
KASP Sequence:
GAGTCATTGGACTTATTGAAGGTCTGGAATATTCATTCAGAGTGTATGCA[C/T]AAAACAATGCTGGAATGAGTCCAGTCAGTGAACAGAGCAAACACAAACTG
Long Flanking Sequence:
ATGAAATTAAAGCCCAGAGTATTATTATCTCATGGGATGTACCCCAAGAAGATGGCGGAGGAGAGATCACCTGCTACAGTGTAGAAAAGCGAGAGACATCTCAAGCAGCATGGAAGATAGTTTGCTCTAGTGTGGTCAGGACAACATTCAAGATACCAAATTTAGTTAAGGGTACAGAATACCAATTTAGGGTGCGTGCAGAGAACAAATATGGAGTAAGTGATCCTCTAACCTCACCAGATGTGGTCGCTCAACACCAATATAAGCCACCAGGTCCACCAGGAAAACCTGTAGTATTCAATGTTACAAGTGATGGCATGACTGTTCAGTGGGATGCCCCAGGTTTTGATGGTGGTTCTCCAATCACTGGATACCACCTTGAGAAGAAAGACAGGAACAGCTTATTGTGGATGAAAGTGAATACCAGTGTTATTTCTGGAAGAGAATACAGAGTCATTGGACTTATTGAAGGTCTGGAATATTCATTCAGAGTGTATGCA[C/T]AAAACAATGCTGGAATGAGTCCAGTCAGTGAACAGAGCAAACACAAACTGGCAATTTCTCCTGTTGGTAAGTTTTAATAATTTTTATTGTCACATCAATCCGTGATGATATTTTACAATGTTTAGGTTTGTAATTGTGCCATTTTTCTCTTATTAGATCCTCCTGGCACACCTAACTGCATTGATGTTACAAGAGACTCTGTAACACTTCAATGGGAACCACCAAAACGTGATGGAGGCAGTAGGATTGTAGCATACAGTGTTGAAAGACGTCAAGGAAGAGCACGTTGGTTGAGATGCAATTTCATTGATGTTAGCGAATGTCAGTTTACAGTAACAGGCCTTGCTGCTGGAGATCGCTTCGAATTCAGGGTAATTGCCAGAAATGCTGTTGGAACAGTTAGTCCACCATCCCAGTCCTCTGGCTACATCATGACCAAGGATGAAAGTGGTATGTACTGGCAAAGGCATCGAGTGCATATTGATCAACATTTTTATTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38759
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 14128 | 17628 | 72 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 27819 | 31319 | 211 | 230 |
ENSDART00000126871 | Nonsense | 17149 | 22089 | 114 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43986485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43111655 |
GRCz11 | 9 | 42913442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACTCTGTGCTGGACAAGACCAAGACATGATGGTGGAAATGAAATTAAA[C/T]AATACATCCTTGAAAGACGGGAAAAGAAGAGTTTAAGATGGGTGAAGGTT
Long Flanking Sequence:
CTGTGTTCTTCAGATACTCCTGGACCACCCGAAGGCCCACTTCGCTTTACAAATATTTCTGCAGAGAAAGCAACTCTTTGGTGGAGCCCACCTGAAAATGATGGCTGTGCAGCCATCAGTAATTATGTGATTGAGAAGCGTGAGACTTCCAGAATTTCATGGGCACTTGTAACATCCAAGTGTGAAGCCTGCTCCTTCAATGCCACAAAACTGATTAAAGGAAATGAATATCAGTTCCGTGTATCCGCTGTCAATAAATTTGGAGTTGGCAAGCCACTAGAGTCTGATCCAATCATTGCTCAGATGCAGTACAGTAAGTAAAGTTGTTCTTGATCTAGTTCTTTGCTTATTTAGTATTGATTGTTCTTTTCTTTAACACATTTTTATATCTCACAGCTGTGCCAGATGCACCTGGAACACCTGACTGTACTCATGTGACAGGAAACAGTATTACTCTGTGCTGGACAAGACCAAGACATGATGGTGGAAATGAAATTAAA[C/T]AATACATCCTTGAAAGACGGGAAAAGAAGAGTTTAAGATGGGTGAAGGTTTCAGCTAAAAGACCAATAACTGAGCTTAGGCACAGAGTAACAAACCTTACAGAAGGGAATGAATATGAATTCCGTGTTATGGCTGAAAATGGTGCTGGAATTGGACCTGCAAGTGGTATATCCAGATTGTTCAAGTGCAGAGAGCCAACAAGTGCACCCAGTGCACCAACTTTGGTGAAGGTCATTGATTCCACCAAGACGTCTGTTACCCTGGCATGGACCAAACCAGTGTTTGACGGTGGTTTGGAAATCATTGGTTACATTATAGAGATGTGCAAGGCAAGCCTTGAGGAATGGCACCGAGTCAACAATCAGACGTGCATCCAGACACATTACAGAGTAACAGAGTTAGAATCAGGTGAAGAATATAAATTCCGTGTTTGTGCTGTCAATGGTGCTGGCAAGGGAGAATTCTCTGAGACTCCACATATAGTACAAGCAGTTGACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1712
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 14431 | 17628 | 72 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 28122 | 31319 | 211 | 230 |
ENSDART00000126871 | Nonsense | 17452 | 22089 | 114 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43985576)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43110746 |
GRCz11 | 9 | 42912533 |
KASP Assay ID:
554-1658.1 (used for ordering genotyping assays)
KASP Sequence:
CACCATCAAATGATGGAGGGGCACGTGTTCATCACTACATTGTTGAAAAG[C/T]GAGAGGCAAGTCGATTAAGTTGGCAGGAGGTCAGTGAAAGGTGCACACGT
Long Flanking Sequence:
GTGAAGAATATAAATTCCGTGTTTGTGCTGTCAATGGTGCTGGCAAGGGAGAATTCTCTGAGACTCCACATATAGTACAAGCAGTTGACAGACTGACCTCGCCAGAAATTGATATAGATGCAGACTTCAAGCAAACACATATTGTAAAGAATGGTGGAACTGTCAAACTTCATATTCCTTTCCGTGGAAAACCAGTTCCACTTGCCACATGGACAAAGGCAGATGGAGATCTTGGTGTAATGGTGGATATAAATACAACCGATACATTCAGCACCTTGACAATTGAAAATTGCACTAGATATGATGCTGGCAAATATACACTCTCTCTTGAAAACAACAGTGGCCGTAAAACCATTACACTAACAGTCAAAGTGTTGGACACACCTGGACCTCCAGGACCTCTTTCATTCAAGGATGTGACAAGGGGTGCTCTGACACTTATGTGGGATGCACCATCAAATGATGGAGGGGCACGTGTTCATCACTACATTGTTGAAAAG[C/T]GAGAGGCAAGTCGATTAAGTTGGCAGGAGGTCAGTGAAAGGTGCACACGTCAAATCCTGCGAGTCATCAACCTTGATATTGGTGTGGCATACTTTTTTAGAGTTACAGCTGAAAATCAATACGGCAAAGGTGAGCCATATGAAATGACAGAGCCTATTATAGCCACAGAAGAGCCTGCATCTCCCAAGCGACTGGATGTCATTGATACAACATCCACAACAGCTAGCCTAGTGTGGATGAAACCTGAGCATGATGGCGGAAGCCGAATTACTGGATACATTGTTGAGACTAGAAAGAAGGGCTCTGCTAACTGGGTTTTTGGAGGTCAAACTAAATCTCTGAAAATGGTTCTTGAAGGCCTGGTTGAGAACACTGAATATGAGTTCCGTGTAAAGGCTCAGAATGATGCTGGCATAAGTCAACCACGAGATGCACTAGCCTCTGTCATTATAAAGGAGCCACGTATAGAGCCAACCGCAGATCTGAGTAGTATAGATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30924
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 15005 | 17628 | 75 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 28696 | 31319 | 214 | 230 |
ENSDART00000126871 | Nonsense | 18026 | 22089 | 117 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 15005 | 17628 | 75 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 28696 | 31319 | 214 | 230 |
ENSDART00000126871 | Nonsense | 18026 | 22089 | 117 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43983572)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43108742 |
GRCz11 | 9 | 42910529 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCCGAGCTGGACAGTAAACTTGTGGGTGAGACAATCTCCATTAGAGCT[G/T]GATCAGACCTTGTTCTTGATGCTGCTGTTGGTGGAAAACCAGAACCTAAA
Long Flanking Sequence:
TTGTGGCTTAATATTTATCCAGTGCTTTTATGTGCATTTTAGATCCACCTGGCACACCAGAAGTTTATGATGTAACCAAGACCTCAGTGTCTATTAGATGGTCTGTGCCATTTAATGATGGTGGCAGCAAGATTGTTGGATATGTGGTTGAACGCAAGGCATCCAGTGATGACGAAGAAGCTCGCTGGTTGAAGTGCAACTACACCACAATCACAGAAAACTTCTTCACTGTTACATCGCTCGTCGAGGGAGAGCAGTATGAATTCCGTGTTATTGCCAGAAATGGTGCTGGAGTTCACAGTATGCCATCTGCATCATCAGGACTTATAACATGCAAAGATGAATATAGTAAGATGGGATTTCTTAATATTTACAGTTGTGTACAACATAAATATGTGCTGATACGAATATTTATTAATACATTTTATTAATTAATTGCAGCACCACCAAAGGCCGAGCTGGACAGTAAACTTGTGGGTGAGACAATCTCCATTAGAGCT[G/T]GATCAGACCTTGTTCTTGATGCTGCTGTTGGTGGAAAACCAGAACCTAAAGTCTTTTGGGCTAAGGGCGACAAGGAGCTGGATCCTGGAGAGAAATACTCTCTGACATACACAAGCACAAGAGCGATGGCAATCATTAAATCATGTGACAGAAACGATACTGGAAGATACATCCTTACTGTAAAGAATGCAAGTGGAATCAAAACATCTGCTGTCAATGTTAAAGTACTTGGTAAGAACATAATAAATAACAGTCTTCATAGTGTTTTATTAAAAAATAAATTTTTACTGCATATTTCATGATAATATATTTTTTGTTTAAGATACACCTGGTCCACCTGCGGGTACAATAACAATCAGCAGGGTCACAGACGAGAAATGCACAGTTTCCTGGAAGATTCCTTTAGAGGATGGTGGAGATCATGTCAGTCACTATATTGTTGAAAGACGCGAGACAAGCAGACTCAACTGGGTCATTATGGAAACTGAATGCAAGACTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41526
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 15005 | 17628 | 75 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 28696 | 31319 | 214 | 230 |
ENSDART00000126871 | Nonsense | 18026 | 22089 | 117 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 15005 | 17628 | 75 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 28696 | 31319 | 214 | 230 |
ENSDART00000126871 | Nonsense | 18026 | 22089 | 117 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43983572)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43108742 |
GRCz11 | 9 | 42910529 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCCGAGCTGGACAGTAAACTTGTGGGTGAGACAATCTCCATTAGAGCT[G/T]GATCAGACCTTGTTCTTGATGCTGCTGTTGGTGGAAAACCAGAACCTAAA
Long Flanking Sequence:
TTGTGGCTTAATATTTATCCAGTGCTTTTATGTGCATTTTAGATCCACCTGGCACACCAGAAGTTTATGATGTAACCAAGACCTCAGTGTCTATTAGATGGTCTGTGCCATTTAATGATGGTGGCAGCAAGATTGTTGGATATGTGGTTGAACGCAAGGCATCCAGTGATGACGAAGAAGCTCGCTGGTTGAAGTGCAACTACACCACAATCACAGAAAACTTCTTCACTGTTACATCGCTCGTCGAGGGAGAGCAGTATGAATTCCGTGTTATTGCCAGAAATGGTGCTGGAGTTCACAGTATGCCATCTGCATCATCAGGACTTATAACATGCAAAGATGAATATAGTAAGATGGGATTTCTTAATATTTACAGTTGTGTACAACATAAATATGTGCTGATACGAATATTTATTAATACATTTTATTAATTAATTGCAGCACCACCAAAGGCCGAGCTGGACAGTAAACTTGTGGGTGAGACAATCTCCATTAGAGCT[G/T]GATCAGACCTTGTTCTTGATGCTGCTGTTGGTGGAAAACCAGAACCTAAAGTCTTTTGGGCTAAGGGCGACAAGGAGCTGGATCCTGGAGAGAAATACTCTCTGACATACACAAGCACAAGAGCGATGGCAATCATTAAATCATGTGACAGAAACGATACTGGAAGATACATCCTTACTGTAAAGAATGCAAGTGGAATCAAAACATCTGCTGTCAATGTTAAAGTACTTGGTAAGAACATAATAAATAACAGTCTTCATAGTGTTTTATTAAAAAATAAATTTTTACTGCATATTTCATGATAATATATTTTTTGTTTAAGATACACCTGGTCCACCTGCGGGTACAATAACAATCAGCAGGGTCACAGACGAGAAATGCACAGTTTCCTGGAAGATTCCTTTAGAGGATGGTGGAGATCATGTCAGTCACTATATTGTTGAAAGACGCGAGACAAGCAGACTCAACTGGGTCATTATGGAAACTGAATGCAAGACTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12712
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Essential Splice Site | 16473 | 17628 | 87 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Essential Splice Site | 30164 | 31319 | 226 | 230 |
ENSDART00000126871 | Essential Splice Site | 19494 | 22089 | 129 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43977299)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43102469 |
GRCz11 | 9 | 42904256 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAGTAGACCAAGAAGAACAGCAATGGGCATTAAAACCAAACTGAGTGG[T/A]AAGTTAATGCAATGCCACTTAGATTTTTTTTTTTCTGAAACAAATTCACA
Long Flanking Sequence:
TACTCTCACTGGCCTAATCCCAGATGCAGAGTACCAGTTCCGTGTGGTTGCTCAAAACGATATTGGTCAAAGTGAGCCTGGTCCTGTGTCCGAGTCAGTTGTTTGCAAAGATCCATTTGGTATGTACACCCCCCCCCCCCATATATATATATAATGTTCTTTTTGTTTGCATCCTTAACTTATTCTTTGTGTTCAACAGATAAACCAGGGCAGCCTGGTGAGTTTGATATTATCTCTATAACCAAGGACAGCATAACCATTCACTGGTTGCGTCCTGAATCTGATGGTGGAAAAGAGATCCTTGGGTACTGGATTGAATTCAGGCAAGCAGGTGAAAGTGCCTGGAAAAAGTGCAATAAAGAACGTTCAAAGGACAGGCAGTTTACCATAGGTGGACTCATGGAAGCAACAGAGTATGAGTTCAGAGTGTTTGCTGAGAATGAAACTGGACTGAGTAGACCAAGAAGAACAGCAATGGGCATTAAAACCAAACTGAGTGG[T/A]AAGTTAATGCAATGCCACTTAGATTTTTTTTTTTCTGAAACAAATTCACAAATGCGAAGTAACTAACATGTTTAAATTGTCTTCTAGTTGGAGAGGCTCCATGCCTGAAGGAGGATATCAAAGATACTACCACTAAATTAGGAGAGTCTGGAATATTAACATGCCAGATTATTGGAAGACCTCTTCCTGAAATTAAGTGGTATAGGTATGGAAAGGAGTTGATCCAGAGCCGAAAATACAAGATGAGCTCTGATGGCCGAAACCACTCTTTATCAGTAATGACAGATGAACAAGAGGATGAAGGCTTGTATACTTGTAGAGCCGTCAATGAGGCAGGTGAAATTGAGACCAGTGGAAAACTTTTATTGCAGGCTGCACCACAATTCCATCCAGGATTCCCATTGAAAGAAAAATACTATGCAGGCTGTGGAACTAGCCTACGTCTTCATGTTGTTTACATTGGTCGCCCTATTCCACAAATCATGTGGTTCTATGGCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25437
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 16688 | 17628 | 89 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 30379 | 31319 | 228 | 230 |
ENSDART00000126871 | Nonsense | 19709 | 22089 | 131 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43976446)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43101616 |
GRCz11 | 9 | 42903403 |
KASP Assay ID:
554-7783.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACCAGTCGTTGTTGATGCTCTATTGAAGAGTTCTGTGATCATTAGTTG[G/A]AAACCACCAAAGGATGATGGTGGATCAATGATCACAAATTACATTGTAGA
Long Flanking Sequence:
TGGAAAACTTTTATTGCAGGCTGCACCACAATTCCATCCAGGATTCCCATTGAAAGAAAAATACTATGCAGGCTGTGGAACTAGCCTACGTCTTCATGTTGTTTACATTGGTCGCCCTATTCCACAAATCATGTGGTTCTATGGCAAGAAGCCCCTCAATCCATCAGAGAATGTTATCATTGAAAACACGGAAAGTTACACTCACTTAGTTATCAGAAATGTCCAGCGTAAAACAAATGCTGGAAGATATAAGGTGCAACTCAGCAACAAATTTGGCACAGTTGACACTGTCCTCCGTGTTGAAATCCAAGGTAAATCAGAGTCTGTTTTAATGAAAAACAAAAAAAACCTGAACTGGCATTACAAATGTTTATTATGCATACAATGTGTTTACAAATGTTACAAAGTTTAAAAACTCCTTGTCTTTTAGATAAACCTCTCTTGCCTGAAGGACCAGTCGTTGTTGATGCTCTATTGAAGAGTTCTGTGATCATTAGTTG[G/A]AAACCACCAAAGGATGATGGTGGATCAATGATCACAAATTACATTGTAGAGAAACGTGAAGCGAAAGAGGGTGAGCAATGGCATCTTGTATCATCGGCTGTCTCAGGAACCACATGTCGTGTTCCAAACCTCATTGAAAGCTCTGGATATTACTTCCGGGTTTCTGCACAGAATCAGTACGGAATTAGTGAATCTCTTGAGATTCCATCTGTTGTCATTATCAAGAGTCCATTCGGTGAGTGTCATGCATTAATTTGTTTTACACTGTATATATGTTTGTGTGTGTGTGTGTGTGTGTGTTTCAACATAACCAAATCCATTATTTAATTCAACAGAGAAACCTGGAGTCCCACAACGGCCATTTGTTTCATCTGTAACCAAGGATTCATGTGTTGTTTCTTGGAAACCACCAACAAGTGATGGAGGTGCCAAAATTAAGAACTATTTCCTTGAAAAAAGAGAGAAGAAACAGAACAAATGGATTGCAGTTACTACAGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21571
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 16926 | 17628 | 90 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 30617 | 31319 | 229 | 230 |
ENSDART00000126871 | Nonsense | 19947 | 22089 | 132 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43975634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43100804 |
GRCz11 | 9 | 42902591 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAAGAAATTTTAGCTGATGGAGCGAAAATAAAGGTCCAAGAATTCAAA[G/T]GAGGTTACTTCCAACTAGTTATCAGCAACGCTGATGAAAATGATGCAGCT
Long Flanking Sequence:
CAAATCCATTATTTAATTCAACAGAGAAACCTGGAGTCCCACAACGGCCATTTGTTTCATCTGTAACCAAGGATTCATGTGTTGTTTCTTGGAAACCACCAACAAGTGATGGAGGTGCCAAAATTAAGAACTATTTCCTTGAAAAAAGAGAGAAGAAACAGAACAAATGGATTGCAGTTACTACAGGAGAAATCCATGAGACATCTTATACTGCTAAAGGTCTTCTTGAAGGATTTGAATATGAATTCCGTGTCAAGTGTGAAAATATTGGCGGAGAGAGTGACTGGAGTGAGATTTCAGAACCAGTCATTCCAAAATCAGATACAGCTCTCCGTGCCCCATTCTTCAAGGATGAATTGAGAGACATGTGTGTAAAATACAAGGCAAACGCAACCTTTGTCACAAAGGTTGTCGGGCATCCCAAGCCAGTGGTTAAATGGTACAAAAATGGCAAAGAAATTTTAGCTGATGGAGCGAAAATAAAGGTCCAAGAATTCAAA[G/T]GAGGTTACTTCCAACTAGTTATCAGCAACGCTGATGAAAATGATGCAGCTGCTTACCAAATTAGAGCTACTAACCAGCTTGGATCAATCTCGACAAGTATGAACCTAGATGTTGAAGGTAAATGTTTCTGATGGTTTATGGTTTTCCTAGCCTTCTTTTCCTTTTCCAAACTATTGTTTTTTTTCTATTTGATATCATGACTTGTCTAATCAGCATTTTTTTCTTCCAGTTCCTGCCAAGATTTACTTACCATTACACCTCCAAGGCATGGGAGCTGTTCATGCCATTCGTGGTGAAGTGGTTACCATCAAGATTCCAATTAGTGGCAAACCTGATCCGGTAGTCACGTGGCAAAAGGGACAAGAGATTATTAACAACACAGCTTACCATCAGGTTATTATCACAAGGTCATTCACCTCCCTGGTGTTCCTAAAGGGAGTACAAAGGAAGGATTCTGGCTACTACATTATTTGTGCCAAAAATCGCTTTGGCATGGATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41525
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | Nonsense | 17611 | 17628 | 91 | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | Nonsense | 31302 | 31319 | 230 | 230 |
ENSDART00000126871 | Nonsense | 20632 | 22089 | 133 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43973465)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43098635 |
GRCz11 | 9 | 42900422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATATGCTGAGTTATTTGTTGAGACTGTCAGGTCCTTCCGTGAGTACTA[C/A]CTTGGACGCTCGCTGAAGAAACCCAGGCGTAGAATTGACAAAAGCAAAAT
Long Flanking Sequence:
CACCCTTGGCTCAGGATGAAATTGGAACATGTTAGTTCAAAAGTCATCAAGACTTTGAGACACAAAAGATACTACCAGTCACTTGTGAAAAAGGAATGGAGCACTGTTGTTTCATCAGCACGTGTTGCCTATGGTGGTGGCTACAGAAACCAGAAAAATGTTTCCATTGGAAGAGTGAAAATTGGACATCCTCAACAAGGCTTGAGAGCAGGACCTATCATGCATGGATCTGCTGAAGAGGGAGGACATGTCAGGTTTGTGTGCTGCATTGAAAACTATGATCGAAACACTGAAGTGACCTGGTACTTTGGTTCCCGCAAATTAACTGCAAGCCACAAATATGAAATTACATATGCTAATGGTGTTGCTAGCATCTATGTTAAAGACATTGAAGAATGTGATGATGGATTATATAGATGCAAGGTTGTCAGTGAAGACAGGGAGGACAATGCATATGCTGAGTTATTTGTTGAGACTGTCAGGTCCTTCCGTGAGTACTA[C/A]CTTGGACGCTCGCTGAAGAAACCCAGGCGTAGAATTGACAAAAGCAAAATTTTGCAGAGGCCACCAGAGTTTACTTTGCCTTTATTCAATCGTTCAGCATACATTGGTGAAGATGTGCGCTTTGGTGTGACCATAACTGTCCATCCAGAGCCAAGTGTTACATGGTTAAAGGCTGGGCACAGAATCAAGCCAGATCCTAAAAAATACACATTCACAAGTGACAAGGGTCTTTATCAGCTCATGATACACAATGTTGACCTCAGTGATGATGCTGAATACACTGTTGTAGCAAACAACAAGTTTGGCGAAGACAGTTGCAAAGCCCGTCTCAATGTAGCACCACATGCTGTTGCTGAGGATACTATGAGACCAATGTTTAAACGTCTCTTAGCCAATATTGATTGTGTTGAGGGGCAGAGCGTCCGCTTTGACTTGAGAGTATCAGGAACCCCAGCACCAACTTTGAAATGGGAGAAAAATGGCAAACCTCTTGAGTTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41524
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000591 | None | None | 7601 | None | 74 |
ENSDART00000017677 | None | None | 17628 | None | 91 |
ENSDART00000059460 | None | None | 7601 | None | 75 |
ENSDART00000109099 | None | None | 31319 | None | 230 |
ENSDART00000126871 | Nonsense | 21395 | 22089 | 133 | 135 |
ENSDART00000138515 | None | None | 400 | None | 10 |
Genomic Location (Zv9):
Chromosome 9 (position 43971177)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 43096347 |
GRCz11 | 9 | 42898134 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTCTGCCTCAAGAACTCACTTGGAGATTCAAGAATTCAAAACAAAGT[T/A]AACCGAGAGACATGAAGTTTCTTCCTTTGAAAAGTATGAATCTCAGAGGC
Long Flanking Sequence:
AGCTGCTCTTAAATCTGAGCGCAAATACCAGGTTGTAACACAGCAACCATTCAGTCTTGACCATGCTCCACGTATCACTGTAAGAATGCGCTCTCACCGTGTACCATGTGGTCAAAACACTAAATTCACTTTGAATGTTCAGTCCAAGCCTGATGCCAATATCCAGTGGTTCCACAATGGACAACAAATACAAGAGAGCCACAAATACCAGTTTACAAATATGAGTGGAGTCCTATCTCTCCAGATTAATGACTGTCAGGCTGAGGACACTGGCACATACCGTGCTCTTTGCACAAATTCAAAGGGTGAGGCATCAGACTATGCAACTCTTGATGTTTCAGGTGGAGCATTTACTACATACTCTTCAAGACGTCGAGATGAGGAGGCCCCGACACAAATTGTACCTGATATAACAAAAACAGATTATTATCATTCAACAACAATCAGAGCTTCCTCTGCCTCAAGAACTCACTTGGAGATTCAAGAATTCAAAACAAAGT[T/A]AACCGAGAGACATGAAGTTTCTTCCTTTGAAAAGTATGAATCTCAGAGGCTTGCATCATCTCCAATTAGATATGCATCAACTGAATACCTATCATCAGCTTCATATTCATCCTCTGAGAGACATACAACATCAGAAAAGCATGTGTCATCTGAATCAAAGTTAAAAGAATCAGAAACATCTGCTGAAGTATCGGTAAAGAAAATTAAAGCTACCCTTTCAGCCAAAATACTCACAAAACCACATTCTCTGATTGTGTCTGAGGGTGACTCTGCACGATTCGTGTGTGATATTGATGGAGAGCCAGCACCAACTGTCACATGGATGCATGAGGGAAGAACAGTTGTCTCTTCACATCGTATTCATGTGTCTACCACACAGTATAAGTCTACTTTGGAAATTTCATCAGTTGAATATTCAGATGAGGGCAACTATACTGTAGTTGTGGAAAATTCAGAAGGAAAGCAAGAGGCAAGATGTACCTTGGCTATTAATAAACCAA
Associated Phenotype:
Not determined