ZMP
COL12A1 (1 of 2)
Ensembl ID:
Description:
collagen, type XII, alpha 1 [Source:HGNC Symbol;Acc:2188]
Human Orthologue:
COL12A1
Human Description:
collagen, type XII, alpha 1 [Source:HGNC Symbol;Acc:2188]
Mouse Orthologue:
Col12a1
Mouse Description:
collagen, type XII, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:88448]
Alleles
There are 29 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32318 | Essential Splice Site | Available for shipment | Available now |
sa23815 | Essential Splice Site | Available for shipment | Available now |
sa23814 | Nonsense | Available for shipment | Available now |
sa37166 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6653 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13062 | Essential Splice Site | Available for shipment | Available now |
sa37165 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43540 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12086 | Essential Splice Site | Available for shipment | Available now |
sa10128 | Essential Splice Site | Available for shipment | Available now |
sa37164 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23813 | Nonsense | Available for shipment | Available now |
sa23812 | Nonsense | Available for shipment | Available now |
sa11564 | Nonsense | Available for shipment | Available now |
sa16630 | Nonsense | Available for shipment | Available now |
sa43539 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43538 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17277 | Essential Splice Site | Available for shipment | Available now |
sa12359 | Nonsense | Available for shipment | Available now |
sa6652 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14083 | Essential Splice Site | Available for shipment | Available now |
sa19245 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10401 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32318
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 331 | 3643 | 8 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49972022)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49857055 |
GRCz11 | 20 | 49660615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACACAACCCCACGCATTAAACATGGCTCCTTTTTCTGTTTATTTTGC[A/T]GTCGTTGAACCAGCGTCAAACTTGCAAGTCACAGAGGTCGCGTCCAAGTC
Long Flanking Sequence:
GATTCCCCAGAGTAGCTGTTGTTATCACAGACGGGAAATCTCAGGACCCCGTGGAGGGTTACGCCAAGAAGTTAAAGAACGCTGGAGTGGAACTCTTCACATTGGGTATGTGGTCGTTCATCATTGCTTATCCTGCTTTCTCACAGAACTGGGAAGCTTACTAAAAAAATCCATCTGCCCCGAAGAAATCCTTGAAAGGAATCTCATGCTCTTATTTATTATTTTCATTCAGGGATCAAAGAAGCAGATGAGGAAGAGTTAAAACAAATGTCTTCAACGCCCTACAGAACGCACGTGTACACGGTGCCAAACTTCGACATGATCAAAGCTGTGGAGAAATCATTCATCGCGCAGGTGTGCAGCAGTGTGGACGACCAGCTCAACTCGCTGGCTAGTGGAGAGGAAGGTAAACAAACAATAACAAGTGTAAACCTGCCGCAGCGGGTTTACTAAACACAACCCCACGCATTAAACATGGCTCCTTTTTCTGTTTATTTTGC[A/T]GTCGTTGAACCAGCGTCAAACTTGCAAGTCACAGAGGTCGCGTCCAAGTCAATGCGGGTGACTTGGGATGCGTCTATTGGGGAAGTGACTGGATACAAGGTGCAGATGGTTCCCATGTTGGCCGGCAGCAAGCGCCAGGAGCTGTATGTTGGGCCGACTCAGACCTCCGTGAATGTGAGGGATTTGTCTCCTGATACAGAGTATGAGATTAGCTTGTTTGCACTTAAAGGTCTGACGCCCAGCGAGGCAGTTATGGCAATGGAGAAAACTCAACCCTTGAAGGTATCATTAGGTAAGAAAGAGTCTACAACGTTGATCTTGTAATGACTGGATTGCTCATTGCGTTATAAACTGCTGAGATGCTATGAAGGTATTTGATCCGCCATCTTACTATTCCCTACTGATAGAGGGCTACAACGTCTGCGCTACAGGGATCATTCAAAAATGGCTTGCGGTACAGCTTGAAAACAAGACAAGATGTTCCCTAAAGTGTATGGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23815
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 722 | 3643 | 10 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49961907)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49847040 |
GRCz11 | 20 | 49650600 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAAAGGAGAAAGCTTTCCGCTATCAGGCTACGAGACCACACTTGACGG[T/C]ACGTGTCTGTATTATTCACATTCATTTTAGCACTTGAGTTTCTACAGAGA
Long Flanking Sequence:
TTAAGGTAGTGGTTCGGTTTAGGTATTGAATAGGGGATGTAAAATAAGATCCTGCAAAACATGCACTTTATAAGCACTAATAATCAGACAATATCTAAATAACAGACTTGTATAAAGAACTAATAGTCAGAATTGGCACTCAAACTCATTTAGTATCAACATTTCTTTATAGAAACCAAAGGAGAAAGCCTCATATCTTCAATTCTGCTTTGCCTTTCAGGTCTGGTTGCTCCCAGGTCTCTGACGTTATCAGAGGTGACTTCCAGGAGCTTCAGAGCTTCTTGGGAAATAGATGCTGTGGATGTTCAGGCCTATCTGGTGCAGTACAAACCCGACGCAGACGCAGAAGCTAGTTATACCTCGGTGTCCATTCCAGGAGACTCTACCACTACCGTTTTATATCACCTTACTCCAGTCACAAAGTACGAGGTTAAGGTTTACGCCCAATATGAGAAAGGAGAAAGCTTTCCGCTATCAGGCTACGAGACCACACTTGACGG[T/C]ACGTGTCTGTATTATTCACATTCATTTTAGCACTTGAGTTTCTACAGAGAGATCTTTATGACCTATATTTTGTGCAGAATTAGGATCTGTTACCAACCTGAAGGTTTCAGAAGAGACCAGCAGCAGTTTTCGGGTGTCGTGGAGGGAGGCTCCTGGTCCAGTGGTGCGGTATAGACTCACATACGTCCCAGTCCAAGGGGATAGTGGCTTGCTGGAAACTGCAACAGTCGGCCCTGAAACCACCATCGTTCTTCAGCAGCTTTACCCAGTTACTACCTACCGTGTCTCTGTGGCAGCTGAATACCCATCAGGCGTTGGGCCTCAAATGCAGATTGATGGAACAACCAAAGAAGGTGAGTGGAAGCATTTTAAGAATTACTTTGAAGGCATGACACTGTAGGGTTATTACAATAGGATATAAGTGTTTACATTGATCTATCCAGGGCTGAGCAATATGACAAAAATCTCATATAGAGTTAAGTGGTGTGCAGGGACGGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23814
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Nonsense | 1117 | 3643 | 15 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49926540)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49811673 |
GRCz11 | 20 | 49615233 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGTTTCCGAGTGACGTGGGACCCCGCTCCCGGTGATGTGCGGGGATA[C/A]AAAGTCACCTTTCATCCCAGCGAAAATGATATTGATTTGGGAGAACTTCT
Long Flanking Sequence:
AAAGTCCAAACATCAGGAAGCATTTTCTTCTCAATCAAACATTAGCTTTAGGTGGCATTTAAAGGCTTAATTGTGTTAATTAGGCAAGTTAAGGTAATTAGGCAAGTCATTGTATCGCGACTGTTTGTTCTATAGGCAATCAAAAACAAATATTGCTTAAGGGAGTTTATAATATTGACCTTAGAATGGTCTTTAAAAAATTAAAAACTGCTTTTACTCTAGCCGAAAATAAAACAAAAAAGACTTTCTCCAGAAGAAAAAATATTATCGGAAATACTGTGAAAAATTCCTTACTACGTTAAACATCATTTGGGAAATATTTGAAAAAGAAAGACTAATAATTCTGACTTCTGCATTATATCGCATTAGCTGATATTCCTGCTTTCTGTTTGTCCTGCAGTGTCTCCATATAAAGCCCCAAGAAACCTACAGACCTCCGAACCCACCAAAACCAGTTTCCGAGTGACGTGGGACCCCGCTCCCGGTGATGTGCGGGGATA[C/A]AAAGTCACCTTTCATCCCAGCGAAAATGATATTGATTTGGGAGAACTTCTTGTTGGACCATACGACAACACGGTTGTCCTTGAGGAACTCAGGTAATGCTTAGAGTAAACTTCAGATGTTTCTCTCAACATGACGAGGCTAATTGTTGTTCTTGTTTTGAGTTGTCACATGTGGTTTCAGTTTGGTGTCTTTGTTTGCAGAGCTGGAACCAAATACTCCGTGGCTGTTTTTGGCATGTTTGACGGAGGTCAGAGTATGCCGCTGGCTGGAGAGGAGAAGACCACCCTCTCTGATGCACCTGATAGCCCTCCTGTTAAATACTCCGGTATAATTTTAGCACGTCATACCAAAGACATCGCATTTACAGTTTGGTTTTAGCAATCGCTTTCAGTTAAGGAAACAAAAATAGTAAAATACTAAAGTTTGGAATCAGGAGTTATAAAGAAACCCAGAAATAAAGATCACTGTATAATTTCAGCACAACATACCAAAGATTTCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37166
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 1383 | 3643 | 20 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49911867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49797000 |
GRCz11 | 20 | 49600560 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTGTGGACGACCTCACTGAAAATCTCTGTAACAGCGTTAAAGGCCCAG[G/T]TACAGTCACACACTTGACTAGTGTACAATTGAAGTTAGAATTATTCGCCG
Long Flanking Sequence:
AATCATCGACTAAACTAACCAAATTTACTGTGTTTTTAAAGGTATGGCCTTGAACTACATCCTCCAGAACAACTTCAGGCCGAATGTGGGCATGAGACCGGATTCCCGCAAGATTGGTGTCCTTGTTACTGACGGCAAATCCCAGGATGAGATTGTAGTGAATTCACAGAGACTGCGTGACTCTGGCATTGAGCTTTACGCCATCGGTGAGTTCTTCTCTTCTTGACACTCTATATTCAGTCACAATTGAATGCAAACATCTGCACGCCGGTAAAAGCTTTTCATCCTGATCTACTGTACGTCTCATTAACCCAGCTGAAGAAATTGAGATCTTTTATTAACTTGGCTCCTAGGTGTGAAGAATGCTGATGAAAATGAGTTGCGATCCATTGCTACCGACCCTGATGAAATCCACATGTACAACGTCAACGACTTCTCCTTCCTGTTGGATATTGTGGACGACCTCACTGAAAATCTCTGTAACAGCGTTAAAGGCCCAG[G/T]TACAGTCACACACTTGACTAGTGTACAATTGAAGTTAGAATTATTCGCCGTCTCGTGAATTGTTTTCAAATCTTTCCCAAATGATGTTTAACAGAGGAAGGAATTTTTCACAGTATTTCCTATAATATTTTTTTCTTCTGGAGAAAGTCTGATTTGTTTTAGATCAGCTGAAAACTTTTTAAGTTTAAGGTCAATAATAATAGCCCCTTAAGTAATCTGTTTTAGATTGTCTACAGAACAAATCTTCGTTATATACTCTCCGGCCACTTTATTAGGTACACCTGTCCAGCTGCTTGTTAGCGCAAAGTTTTAATCAGCCAATCACATGGTAGCAACTCAATGCTCTTGACATGGTCAAGATGATCTGCTGCAGTTCAAACTTTCTTTAAATGGGAAAGAAAGGTGATTTAAGTGACTTTGAACCTTGTATGGTTGTTGGTGCCAGATGGGCTGGTCTGAGTATTTCAGAAACTGCTACTGGGATTTTCACGCAGAACCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6653
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Nonsense | 1452 | 3643 | 22 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49903892)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49789025 |
GRCz11 | 20 | 49592585 |
KASP Assay ID:
554-5114.1 (used for ordering genotyping assays)
KASP Sequence:
GGYGAGGAAAACACACTTGTCCTGGTCAACCTGAACCCCATGACCGAGTA[T/A]ATCGTCAGGGTCTATGGAGTGATCGGGGAGGAGAGCAGCGAACCTTTGAA
Long Flanking Sequence:
AATTAGGCTGTGTGATAATCTGTGCAAATAATCTGGTCACCATTACTGTGCCCGTTGCTATAAAAGTCAGGTTTGATGAAGTACAACATTTGACATTTAATTTCCACATCTCTGCATACCTCTGTATAATCTTAATGACTTCAATAAAACAGGGCAGCTTTAACGTCACATTCCTTCAGAGCTATGCAGTTCTCATATATTATTGTAATGTCAACATTGTGTGCATTGGGGAAAGTCTATATGTTTTAAAGGTATTGTGTATCAGTATGAGCTGATCTAGATACCATAAATCCCACAACCTGCCCTGCGTGTTTTGAGCTGAATTCCGACCTCTTAGAAGCAGCAACTTCAGAGAGAAGATTTCAGATGGCTTCACCCCTCCGCTTGTATAATACCCCTCTCAGCAGACAATCACCGCTCTCTGATGATGTTTTGCAGCTGTTCGTTGACGGTGAGGAAAACACACTTGTCCTGGTCAACCTGAACCCCATGACCGAGTA[T/A]ATCGTCAGGGTCTATGGAGTGATCGGGGAGGAGAGCAGCGAACCTTTGAAAGGAACCGAAACCACATGTAAGTCAAGCAGATCAACCCTTCTCCTGCTGTTTATTGCAACTGTTTAGTCTCATTGTCTGAACTAAACATTAACCACTGGAAACAGCTGTTTCCCTGCACACTACAGCTGTTTTCACAGACTTGATATCTGTCGCTTTGTACATATGGAACTACCTTTAAGGAAAGACTACACTTTGTTTCAACACAGGCTCATTGTGAGAATGTACTTCCATATACATTTCTGGAGAGCGCAAATTATGTAGCCAGAGCTATCTTATTTTTAAAACTCTACAGGGCAGTAAGACGTCGTAGATGACTTCAGTTTTGTTTTCCGCTCTACCAGCTGACCGCTTACCTCGGTGTGGATGTCTTTACCGTCAGTTTGCCCAGTGGCTCGCCGCATACATCAGCAGACTTGAGACGCAGTTGACCGCAACAACGCTGTTCGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13062
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 1566 | 3643 | 24 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49896651)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49781784 |
GRCz11 | 20 | 49585344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGCAYGGAGWGGCGGCCAGCCAACCGCTCATTGACAGAGGAGTCACTC[G/A]TATGCTAGTCTTCYYAATGCTTTCWGATGGTTTCCATTTGTYATTGTCAA
Long Flanking Sequence:
TTCTTTGTTAATTTTTTTTAATTGTAATATTGGCGGCGCAGTGGGTAGTGCTGTTGCCTCACAACAAGAAGGTCGCTGGTTCGAGCCTCGGCTGGGTCAGTTGGTATTTCTGTATAGAGTTTGTATGTTGTCCCGGTGTAAAACAAAACAAACATCATGGATATCTTGTTACAATACTTTTGCATAATTCTATTTCTATTTTAAAAGTAAGTAAATTTAAATGAACTTTTAAGTCATTACAAAGGTATGTAAGCTTTGGTTGTTTTTATCTTCCAAATGTGAAAGTTGTAGCACGCAAGCTTGGATACCCTGATAGACTTACATACTGATGCCAACTTTATTTAATTTGACGTGGACTTCCCTCTTGCAGATGCGAGTCGGTGCAGATGTGAATGACGTCCAGCTACTGCAGCTGCTTCCAAACACGGCGTACTCGATCTCCCTGTTCGCCCTGCACGGAGAGGCGGCCAGCCAACCGCTCATTGACAGAGGAGTCACTC[G/A]TATGCTAGTCTTCTTAATGCTTTCAGATGGTTTCCATTTGTTATTGTCAATATGTATTATATGTGCTTGTTAATCTGTCTGTCCGATGTAGTGCCTCTCCCTCCAGCCGGTAAGTTGAAAATCACAGAAGTGACCCACAGCTCTATGCGTTTGACCTGGGATGCGGCTCCTGGGAATGTCAGGAAATACATCATCACGTACAAGCGTGAGGACGGGGAACTGAAAGAGGTGAGTGAAATGTGCAATTCGCATTCTACACAATTGATTTGGGTTGGGACAACATGAAGGATTTAAGATAGCTTATTAGCTTTTACAAATTTAAGTTGATTGAACATAAAACAATTAAGTTGTCCCCCATAAATACACCAAGAGTTGTGTTGTTTCAGCTTATTTTAAAGAAGTAGTTTGAACAATGTTTTTTGAGTGTAGTAAGATCATCAAAAGCAATGTGCTTACATTAAAATATAAATACAATGTGCTTGATGTGTTCGTAATGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37165
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Nonsense | 1641 | 3643 | 26 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49893356)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49778489 |
GRCz11 | 20 | 49582049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAACCTGCGCTCTCAGACCGAGTATGATGTTGCCGTCACTCCAGTTTA[C/A]GACGAGGGTTCAGGAAATCCCATGCTTGGCACTGCAATAACTGGTGAGCT
Long Flanking Sequence:
TCAGCTGCAGATGTGCATGAATGGCGGAAGAAAGTAGTTCCTAGTACAAAAGGGTTTTAGACTCTCTGTGTTAGATTTTATTTTTTTATGTACAAGACTTTGCCGTCGAACTGTTGTATAAATGCAATATCACACTCGTAGCAGTGTGCAATGGCTGTATATCAGCACTGGTGGGGCACTAAGACACTCGGCCTGCAGCCTCGTGCCCACGCACGCTGATATACAGCCATAGCACACTGCTACTCGTGTGATATTGCTCATATATTAAATATATATTCAGTGTTGGAAACATTCATTTAAAAAGTAATTAGTTAAGTAACTTATGAATTATAGCCGAGTTGGTAAGTGAATTACATCCAGGGCTTAACATTAACACCCGCCAAACGCGTTCATGTCGATTCTGTTGTTTGACAGTTGGAGGTCAACGGTGACATCACCACCATGGTTCTTACCAACCTGCGCTCTCAGACCGAGTATGATGTTGCCGTCACTCCAGTTTA[C/A]GACGAGGGTTCAGGAAATCCCATGCTTGGCACTGCAATAACTGGTGAGCTTCAAATCCGCAATTGATTCTCCGAGTCGACTCTATTGACTGATGATGTTGGTTTGGCAGCAGCGTTGCTTCACTGCTGCTGGTTTTTGTTTGTGCTACGCTGGTGTTCAACTGTGTGACTTGCTGGTTACAAGACCTGCTATTTCAGCAAGTCTTTTCAAGCTCCCCTCCGTCTGCATAATGGCTGCCATGTGTGACGCCACCCTTACCCAAGCCACGTGCATACTGTATGTTCATAACTTGACTTTATCAGTCCCACGGGTGAATCATTTATTAGTTCCAGATGATCCACAAGTAGCTCCCCTTTACATAGGAACGTGCAGTAACATTTCAGTATAGGGACCAATTTCTTATTATTAACTAGTGACTTAGTACCTGCCTATTATTAAGATTTTGGCTGATTATTAGTACTTTTAAAGCACATATTCTGCATGTTTTTATTCTATATTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43540
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 1794 | 3643 | 29 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49883155)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49768288 |
GRCz11 | 20 | 49571848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCTACAAAGTCACCCACCAGCCCGTCGCTGGAGGAAAACCATTATCT[G/A]TAAGTTCAGCTGCCCCCAAATCTCCCTCCAGTGAGATCTTTTGAAGCCAG
Long Flanking Sequence:
CCCTTTAGAACAGGAGTGTCAAACTCAATTCCTGGAGGGCCGAAGCCCTGCACAGTTTAGTTCCAACCCTGCTCCAACACACTTACCTGTAGGTTTCAAACAAGCCTGAAGGACTCAATTAGTTTGATCAGGTGTGTTTAATTAGGGTTGGAACTAAACTGTGCAGAGCTGCGGCCCTTTTGGAACTGAGTTTGACACCTGTGCTCTAGAAGGACAGAAATGATTATTAACCATATTCATAATATGAAATCAGATCCTGAATCAATAACATTCCTCATGATTCCCAACCCTAATACTCTGAAAGTATGATTTTTTTCATTTTTATTTCATTTGGCTAATTGAGTTTCCGTCTGCTCCCAGTGCCCACTGGACCCCCACAAAACCTCCAGGTCTTCAACGCCACCACAACAACCCTAACTGTGAAATGGGACCACGCACCAGGCCCTGTCCAGAGCTACAAAGTCACCCACCAGCCCGTCGCTGGAGGAAAACCATTATCT[G/A]TAAGTTCAGCTGCCCCCAAATCTCCCTCCAGTGAGATCTTTTGAAGCCAGGCACGGTTAATCTTTCACTTATGATGACCATGATGAGTCGCAGGATCTGTTTTTTTGAAGTTTGAGGACCTTGTGTTAGTCATTATAGCGAGCTTGCCGCTGTAAGCGAGATGAAAACATCATGACAGGAAGTCATTACAAACAGACTCATCTCATGCAAACCATATCAACATGTCTGCCATGTAGCCCTCGCTATCAATCAACATACAAAACCATCATTGTTATATATTTAATGTGAAGTGCGCCCGAGGTGAACATCCTAGCAAACTGTTGTTGTTCGTTTAGGGATTGTTTGGCTAACAATATTCAAATTGAACAATGGGGCTGTCAGTAGTTTGTTTATTAATTGAAGATCAACTGCTGCAAAACTATCGGATTTTGTCATATTTACTAAGTAATACAAAGTTCAAATATGGAAATCTGATATATGGCCATATATAAACGCACGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12086
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 2108 | 3643 | 37 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49867651)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49752784 |
GRCz11 | 20 | 49556344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGAYGCATTGCAAAAAGACGATGTTGATWKAACTATTGTTGTCTTCTT[A/G]GAACCTTTGGGTAGCGTGAGGAACCTGCAGGTWACAGATCCTACTATMAG
Long Flanking Sequence:
GTGAAGTCGAGTTAATAAAGCATTTATTAACATACATAGTAACCATTAATATATGCCTGAATAATAAGACATATAAACATTAATTTCAATAGTTTATCAATCATTTACTAACTCATTCTGAATGATCCTAAAAACCCTCAACTACTCTTAAATACAACTGTTTTGTAAATAATGCAATACTTGATTTAGTAATGAAAAATTAATCATTTACTAAGTATGAAAATACAATTATTAAGCACATTTTAAATGTGGTTATAAGTCAAGAATAGAGCATTTGATGCTGCAGTTATAAACTGCTTACTAACGTTTATTAATGTAGAGTTAATGCTTAGCGGATAATGAATTCACTATTTGCTAATGCCTAATAAATGATTTATAGTGTGTAGTTATTATAAAGTGTTACCGCATTTTCTCACACTCAAGGATCATATATAAATAAATGAAGAATGTCTGGACGCATTGCAAAAAGACGATGTTGATTGAACTATTGTTGTCTTCTT[A/G]GAACCTTTGGGTAGCGTGAGGAACCTGCAGGTTACAGATCCTACTATAAGCACCTTGAATGTACGCTGGGAGCCAGCAGAAGGCAATGTGCGGGAATACATAGTCATTTACGTTCCTGCTGGTAGTCAAGATCAAGAAGTGGTAAGAACGATTTCCGTTTTTGAAGAATTTCGAGGGGATCACATGCTTATGATTGCTTGCAGCTTCCCCTGCATTATCCAATTGATTATTCACCAACCACACGATTCCTAGGCCACTATAAGAGCCCTGGGTTTCATACCACAGGCATCTTCGTTTTGAAGAATCCCCCCTTCCACCCCTACTCCTCCTCCTCTTTCCAGATGGGTGGCACGGTGGCCCAGTGGTTAGCACTGTTGCCTCACAGCAAGAACGTCGTTGGTTCTGGTCATCATCAAAACCAGCAGACGTTTCTGTGCAGAGTTTGCACGTTCTCCCTGTGCTCGCGTGGGTTTCCCCCGGGTCACCTTTTTCCTCCCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10128
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 2108 | 3643 | 37 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49867651)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49752784 |
GRCz11 | 20 | 49556344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGAYGCATTGCAAAAAGACGATGTTGATWKAACTATTGTTGTCTTCTT[A/G]GAACCTTTGGGTAGCGTGAGGAACCTGCAGGTWACAGATCCTACTATMAG
Long Flanking Sequence:
GTGAAGTCGAGTTAATAAAGCATTTATTAACATACATAGTAACCATTAATATATGCCTGAATAATAAGACATATAAACATTAATTTCAATAGTTTATCAATCATTTACTAACTCATTCTGAATGATCCTAAAAACCCTCAACTACTCTTAAATACAACTGTTTTGTAAATAATGCAATACTTGATTTAGTAATGAAAAATTAATCATTTACTAAGTATGAAAATACAATTATTAAGCACATTTTAAATGTGGTTATAAGTCAAGAATAGAGCATTTGATGCTGCAGTTATAAACTGCTTACTAACGTTTATTAATGTAGAGTTAATGCTTAGCGGATAATGAATTCACTATTTGCTAATGCCTAATAAATGATTTATAGTGTGTAGTTATTATAAAGTGTTACCGCATTTTCTCACACTCAAGGATCATATATAAATAAATGAAGAATGTCTGGACGCATTGCAAAAAGACGATGTTGATTGAACTATTGTTGTCTTCTT[A/G]GAACCTTTGGGTAGCGTGAGGAACCTGCAGGTTACAGATCCTACTATAAGCACCTTGAATGTACGCTGGGAGCCAGCAGAAGGCAATGTGCGGGAATACATAGTCATTTACGTTCCTGCTGGTAGTCAAGATCAAGAAGTGGTAAGAACGATTTCCGTTTTTGAAGAATTTCGAGGGGATCACATGCTTATGATTGCTTGCAGCTTCCCCTGCATTATCCAATTGATTATTCACCAACCACACGATTCCTAGGCCACTATAAGAGCCCTGGGTTTCATACCACAGGCATCTTCGTTTTGAAGAATCCCCCCTTCCACCCCTACTCCTCCTCCTCTTTCCAGATGGGTGGCACGGTGGCCCAGTGGTTAGCACTGTTGCCTCACAGCAAGAACGTCGTTGGTTCTGGTCATCATCAAAACCAGCAGACGTTTCTGTGCAGAGTTTGCACGTTCTCCCTGTGCTCGCGTGGGTTTCCCCCGGGTCACCTTTTTCCTCCCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37164
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 2244 | 3643 | 39 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49863428)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49748561 |
GRCz11 | 20 | 49552121 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATTACAAAGTGTTCTACATCCCGCAACCAGGAGATGCTGAGATGATGG[T/A]AGGATCTGAAGAACTAACTTCTAATGGCTTATATTAAGGTCCTTCCACAT
Long Flanking Sequence:
ATTTGCTCTTCAGTGTTTGGACTCTCAGTAACGATTTTAAACCACACTGAACTGAGCTAAACTGAATTGAACCTAAACACTAAAAACTGAACTACCCTGATCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCCTCACAAATAAAGCTGAATTGAATTGAATAGAATATATTTAGACCAATAGCAAAAGTGGATTCCAACACACCCTGCATTGTGCGCTTTATACTATGAGCTTATGTTGTTAAAATGGAGCCCACAGTGTAATACATCTTCTGATAAACAAGACTACTGGCAATTACTTCTTTAACAGTGACTGAGTATCTTTGTTTTTAGAACCACTGGGTGGAGTTCGCAACCTTCAGGTTACCGATCCCACCAGCAGCACCCTAAATGTGCGATGGGAGCATGCCGACGGAAACCCACGCAATTACAAAGTGTTCTACATCCCGCAACCAGGAGATGCTGAGATGATGG[T/A]AGGATCTGAAGAACTAACTTCTAATGGCTTATATTAAGGTCCTTCCACATTATGTGAGCCTCTTTTCTGATTTGCTGTGAACAGGAACTAGTGTCCGGTGGCACGACAAGTACCGTCCTACGTAATCTCAACGCGAACACCATGTACAAGGTCACATTGTTGCCCATGTATGAAAATGATGTGGAAGGAAAACGTCAGTCAGAGAATGGAAAGACAAGTGAGTGCAGTCCTTTGCAACTTCTACATTTCAGATGGAGAACTGATCTACTGTACTTCTGAGGGATCACTGACTACATTGAGGCACAGGTTATGTGTGTTCAGGTATGTTTTTTTTATTGACGCAGAACCTTTGGGAAGTGTGAAGAACCTTCAGGTGACTGACCCGACTGTCAACTCTTTGAGAGTGAGATGGGATGCTGCAGATGGGGATGTTCGCCAATACAACGTCATTTATGTTCCTGTTGCCGGAGGTGCTGCAGGCCAGGTAATGACCTAAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23813
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Nonsense | 2372 | 3643 | 42 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49862747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49747880 |
GRCz11 | 20 | 49551440 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTACAAGGTCACTGTAGTACCAGTATATGCAGATGCTGAAGGAAAGAGA[C/T]AGTCAGCGAATGGAAAAACAAGTGTGTACCTCTAGTCAACACTTTGAATG
Long Flanking Sequence:
GTGGAAGGAAAACGTCAGTCAGAGAATGGAAAGACAAGTGAGTGCAGTCCTTTGCAACTTCTACATTTCAGATGGAGAACTGATCTACTGTACTTCTGAGGGATCACTGACTACATTGAGGCACAGGTTATGTGTGTTCAGGTATGTTTTTTTTATTGACGCAGAACCTTTGGGAAGTGTGAAGAACCTTCAGGTGACTGACCCGACTGTCAACTCTTTGAGAGTGAGATGGGATGCTGCAGATGGGGATGTTCGCCAATACAACGTCATTTATGTTCCTGTTGCCGGAGGTGCTGCAGGCCAGGTAATGACCTAAATCTTAATCATCTCAAATTGTCATTTTAATGAGTTAGTTGCTAAATGATATGTGCTCACACTGATGTGCTCTACAGACCCAAGTGTCTGGAATGTCCACCAACACTATTCTAAGAAACCTGCAACCAAATACGGAGTACAAGGTCACTGTAGTACCAGTATATGCAGATGCTGAAGGAAAGAGA[C/T]AGTCAGCGAATGGAAAAACAAGTGTGTACCTCTAGTCAACACTTTGAATGTAATTCGTTAGCATGCAAGATACTTCATTTCAGTTTTACCAATTTTCAGAGCCTCTGGGTGGAGTGAAGAACTTGCAGGTCACCGATCCCACAACCAGCTCACTGAAGGTGCGCTGGGAGCCTGCGGAGGGAAACGTCCGACAGTACAGAATCTTCTACGTTCCAGCATCTGGTGGTGCAGAGGACATGGTAGGAGATGCTCAACAGAAGAAGCTCTACTGTAATTCTTGACAACCTTTGATCTTCTATAACCATTTCAACTTCACATCAACAGGAGCAAGTTTCTGGAGGCACCACCAACACCATACTGAGGAACCTTCTGTCAGACACAGTCTACACAGTGACGGTGGTTCCTGTTTACCCTGAGGGGGAGGGTCTCCGTCAGTCTGAAAAGGGAAAGACTCGTAAGTTGTGCTTGGAAATTATATGCATGCTTGAATGAATGCGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23812
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Nonsense | 2387 | 3643 | 43 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49862623)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49747756 |
GRCz11 | 20 | 49551316 |
KASP Assay ID:
2261-4959.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATTTCAGTTTTACCAATTTTCAGAGCCTCTGGGTGGAGTGAAGAACT[T/A]GCAGGTCACCGATCCCACAACCAGCTCACTGAAGGTGCGCTGGGAGCCTG
Long Flanking Sequence:
AGGTTATGTGTGTTCAGGTATGTTTTTTTTATTGACGCAGAACCTTTGGGAAGTGTGAAGAACCTTCAGGTGACTGACCCGACTGTCAACTCTTTGAGAGTGAGATGGGATGCTGCAGATGGGGATGTTCGCCAATACAACGTCATTTATGTTCCTGTTGCCGGAGGTGCTGCAGGCCAGGTAATGACCTAAATCTTAATCATCTCAAATTGTCATTTTAATGAGTTAGTTGCTAAATGATATGTGCTCACACTGATGTGCTCTACAGACCCAAGTGTCTGGAATGTCCACCAACACTATTCTAAGAAACCTGCAACCAAATACGGAGTACAAGGTCACTGTAGTACCAGTATATGCAGATGCTGAAGGAAAGAGACAGTCAGCGAATGGAAAAACAAGTGTGTACCTCTAGTCAACACTTTGAATGTAATTCGTTAGCATGCAAGATACTTCATTTCAGTTTTACCAATTTTCAGAGCCTCTGGGTGGAGTGAAGAACT[T/A]GCAGGTCACCGATCCCACAACCAGCTCACTGAAGGTGCGCTGGGAGCCTGCGGAGGGAAACGTCCGACAGTACAGAATCTTCTACGTTCCAGCATCTGGTGGTGCAGAGGACATGGTAGGAGATGCTCAACAGAAGAAGCTCTACTGTAATTCTTGACAACCTTTGATCTTCTATAACCATTTCAACTTCACATCAACAGGAGCAAGTTTCTGGAGGCACCACCAACACCATACTGAGGAACCTTCTGTCAGACACAGTCTACACAGTGACGGTGGTTCCTGTTTACCCTGAGGGGGAGGGTCTCCGTCAGTCTGAAAAGGGAAAGACTCGTAAGTTGTGCTTGGAAATTATATGCATGCTTGAATGAATGCGGAATATAAGCTCAGAATTAGCATGCAACAATAGCTATGCTTTCATCCACCTATTGTCATGTGCATTTTGGAATATTGCATACGCTATGACAACATCTTGTCACGGTTTCAGGAAGGGAATGAGAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11564
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Nonsense | 2537 | 3643 | 46 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49852492)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49737625 |
GRCz11 | 20 | 49541185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCAACCTCAACAATGCTTTCCTGGATCAGCTCGTTCCAGATACTCCGTA[T/G]TCGGTGAATGTGATGGCGGTGTATGCTGAWGGAGAAGGCCCAGGGATTGA
Long Flanking Sequence:
TGTGTGCTGACCCATATTAGTCGAACACATCAGTTTGAGCCGGAGCTAATTCTGTCATGAGCTTTAGTGTATGAAAGGAATGCAGCAGCCTCTAAATGAACACATGCACAGATGTGGTGATAATCCCGCAGGGTGTTGACAGGTTACTGATGGGGTTTCCCTGTCACCTCCGATCCAGTCTCTCTTCAGCTCTAGCCGCCCCCGAGGGAAATTACACGCATTTGACAGTATTTATGTAGCATTTAACCCTGTGAGCACATCTGTTTGCATTACTTATCTGTTTGGAAATGTTATCTAGCCCTGCTAATCTAAACATGGGGCTTAACCAGTGACGTAATTCTGTATGTTCACTTTGCCAAACTCTTAAGGGTTGTAATACAGTGGATGTTTGTAAATATATTCTCCTCCATGTTATCTAAACCACGGGCTTCTCCTCAGGTTCTCGTTCCTGGCAACCTCAACAATGCTTTCCTGGATCAGCTCGTTCCAGATACTCCGTA[T/G]TCGGTGAATGTGATGGCGGTGTATGCTGATGGAGAAGGCCCAGGGATTGACGGAAATGGAAAAACATGTGAGCTAAATGATTAAATATGATGTTTTTTGCATGTACTGTGCAAAAAAAGTTTGTTTTTTTAATTATTGTACAGTTGAAGTCAGATTAATAAGCCCCCCTGGATATTTTCCATCAATTTCGGTTTGATTAAAAGAATATTCAACCATGATATCCTTCCATGATAACTGAAAGGTGGATAAAAGCATGACTTTTTCACCTATGCTTATGTTTATAAACAATTGCTGCCATTTTTTTCTTTGTCAATAAGCCACTTAAATTGGACACACATCACAGTATGCATGAAAAGATCTTTCAATACTTTCATTTCATTGCAACTTCACAACACTCACAGCATCCACATGGCAGCACAACCACTTATAATAACTTGGCTTTCGTAAATGTTGTCTGTTTCAGTACCACGAGCTGGACCCAGGAATATGAGGGTCTTCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16630
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Nonsense | 2562 | 3643 | 47 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49852023)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49737156 |
GRCz11 | 20 | 49540716 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCACTTATAATAACTTGGCTTTNCGTAAATGTTGTCTGTTTCARTACCA[C/T]GAGCTGGAYCCAGGAATATGAGGGTCTTCGAAAYCACCACAAGCACCRTC
Long Flanking Sequence:
TCCTGGATCAGCTCGTTCCAGATACTCCGTATTCGGTGAATGTGATGGCGGTGTATGCTGATGGAGAAGGCCCAGGGATTGACGGAAATGGAAAAACATGTGAGCTAAATGATTAAATATGATGTTTTTTGCATGTACTGTGCAAAAAAAGTTTGTTTTTTTAATTATTGTACAGTTGAAGTCAGATTAATAAGCCCCCCTGGATATTTTCCATCAATTTCGGTTTGATTAAAAGAATATTCAACCATGATATCCTTCCATGATAACTGAAAGGTGGATAAAAGCATGACTTTTTCACCTATGCTTATGTTTATAAACAATTGCTGCCATTTTTTTCTTTGTCAATAAGCCACTTAAATTGGACACACATCACAGTATGCATGAAAAGATCTTTCAATACTTTCATTTCATTGCAACTTCACAACACTCACAGCATCCACATGGCAGCACAACCACTTATAATAACTTGGCTTTCGTAAATGTTGTCTGTTTCAGTACCA[C/T]GAGCTGGACCCAGGAATATGAGGGTCTTCGAAACCACCACAAGCACCATCAGCATTGGCTGGGATCATGCGGAGGGTCCTGTACAGCAATACAAGATTTCATATGCTTCGTTGACGGGAGATCCCATCACAGAATTTGTGAGTAAAAGTCTATAGCAGGGGTGGCCAACCCTGTTCCTGGAGAGCCACCTTCCTGCAGATTTCAGTTGCAACCCATATCAAACACACCTGCCTGTAATTATCACGTGGTGTTCAGGCCCTAATTAATAGGTTCAGGTGTGTTTGATATGGGTTGCAACTGAAATCTGAAGGAAGGTGGTTCTCCAGGAACCGGGTTGGCCACCCCTGGTCTATAGTGATTATTGCTACCGTACATTTGCACGTTTAGTTAGTTTCTAATGCAGCCCAGCTTTCAGGGAACATTTACAGAACGTTCCTTAAAAGTTGTAAATGTGATCACAGAACATTAGTACTACTTTCTACTAACTTTTCTCGAACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43539
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 2651 | 3643 | 49 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49847607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49732740 |
GRCz11 | 20 | 49536300 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACACAAGCCTCTAGCTGATATTTTGCTCTTACTTTGCATTTTCTGTTC[A/G]GTCGGTCTACTGGCACCTCAGAACCTGCGAGTCTCAGACGAGTGGTACAC
Long Flanking Sequence:
CCTTTTTACAAGTCTGATGTGCCTAAAGTGTGTATGTGAAGTTTAAGCTCAAAATACCACACAACTAATGCTTTATAACTGCCCCTTTTTGGATTTGATCTTAATTGTGGTATTTTGGTGACTGTCACTTTAAATTTAAATGAGATTGTGCGCTTTCGAAAGAGGGCGGAGTTATATGTACCTGTGCCAGCATAGTGGCAGATTCAAAAACAAGACTAACGTCCTATGCTATAGTGGGCGGGGCTTTCCCCCTCTGATGACACGTATAACAGGAGAACGTCAATCAAAGTGTTTCTGCAAACTGTTTTGATCAAATCTGATTACATTATATTATTATTTATATATTTTTACCATTTAAAGCCGGTTATATTCACAGACTGTTGCCACACAACTGTGTTAAGACAGGTACTTTTGGATAGTATGTCTCCTTTAATGCACTTCTCAGTACTATGACACAAGCCTCTAGCTGATATTTTGCTCTTACTTTGCATTTTCTGTTC[A/G]GTCGGTCTACTGGCACCTCAGAACCTGCGAGTCTCAGACGAGTGGTACACGCGCTTCCGTGTGTCCTGGGATCCTGCTCCCTCTCCAGTCATGGGCTACAAACTGGTCTACCAACCAACAAGTACGAAACATTGCAGTATTATGACTGGTAACACTTTACAATAAGGATGTATTAGTTAATATATGTATTAACATGAACAAACAATGAATAATGCATTATTACAGTATTTATTCATGTTAGGTAATGAACATATAGTCATTCATTGTCTGTTGATGTTTCTGTCACGATCACATAAAAGAAGACTTGGAACCCAACTGCAAGTAAAAATAGACTTTTAATGAAGATCTCACAAAAACAGGTAAGAAGGTGACTGGAAGTAATAAAGATCCGTGTAGAGGAAATAATCAGAATAGAGCTGGATCAGCGGCGCCGATTAAATGTTCATGATAAACATCAACAGAGAGGATCAATCATTCATCTTCGATGAAAGCAGGAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43538
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Nonsense | 2660 | 3643 | 49 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49847579)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49732712 |
GRCz11 | 20 | 49536272 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTACTTTGCATTTTCTGTTCAGTCGGTCTACTGGCACCTCAGAACCTG[C/T]GAGTCTCAGACGAGTGGTACACGCGCTTCCGTGTGTCCTGGGATCCTGCT
Long Flanking Sequence:
TGTGTATGTGAAGTTTAAGCTCAAAATACCACACAACTAATGCTTTATAACTGCCCCTTTTTGGATTTGATCTTAATTGTGGTATTTTGGTGACTGTCACTTTAAATTTAAATGAGATTGTGCGCTTTCGAAAGAGGGCGGAGTTATATGTACCTGTGCCAGCATAGTGGCAGATTCAAAAACAAGACTAACGTCCTATGCTATAGTGGGCGGGGCTTTCCCCCTCTGATGACACGTATAACAGGAGAACGTCAATCAAAGTGTTTCTGCAAACTGTTTTGATCAAATCTGATTACATTATATTATTATTTATATATTTTTACCATTTAAAGCCGGTTATATTCACAGACTGTTGCCACACAACTGTGTTAAGACAGGTACTTTTGGATAGTATGTCTCCTTTAATGCACTTCTCAGTACTATGACACAAGCCTCTAGCTGATATTTTGCTCTTACTTTGCATTTTCTGTTCAGTCGGTCTACTGGCACCTCAGAACCTG[C/T]GAGTCTCAGACGAGTGGTACACGCGCTTCCGTGTGTCCTGGGATCCTGCTCCCTCTCCAGTCATGGGCTACAAACTGGTCTACCAACCAACAAGTACGAAACATTGCAGTATTATGACTGGTAACACTTTACAATAAGGATGTATTAGTTAATATATGTATTAACATGAACAAACAATGAATAATGCATTATTACAGTATTTATTCATGTTAGGTAATGAACATATAGTCATTCATTGTCTGTTGATGTTTCTGTCACGATCACATAAAAGAAGACTTGGAACCCAACTGCAAGTAAAAATAGACTTTTAATGAAGATCTCACAAAAACAGGTAAGAAGGTGACTGGAAGTAATAAAGATCCGTGTAGAGGAAATAATCAGAATAGAGCTGGATCAGCGGCGCCGATTAAATGTTCATGATAAACATCAACAGAGAGGATCAATCATTCATCTTCGATGAAAGCAGGAAGCATTAAGAAACTGCAACAAGGTATCAACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17277
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 2739 | 3643 | 50 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49845028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49730161 |
GRCz11 | 20 | 49533721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAATATGATGGCGGWGTCAGCAAACCTCTCATCGGACAAGGAACAACAT[G/A]TATGTAAAGAAACAAAGCTCRTCTGATTTCATYGGACGTATCCCWTCCTC
Long Flanking Sequence:
GGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGTTGAGGTTCGAACCAGCGACCTTCTTGCTGTGAGGCGACAGCACTACCTACTGCGCCACTGCCTCGCCCTTAGCTAATGTTAACAAGCATAAATACGTACTTTAATAATGCATTAATAAATACTGAACTATGATTAATAAAGGCAGTACATGATTTGTTAAGTATAAGTTAATATTAGTAAATACATTAACTAATGAAACCTTATTGTAAAGTGTGACCTTATGACCCAAGACACTGCAAGCCCTCATGACAATTCAATTACAATTCATCACAGCTCTTTATTTGCTAAATGTGTCTTTTTGTGTTTTTCTTTAGCTAAAGATGAATCTTTGGAGGTGTTTGTTGGTGACGTCACCAGCTATACCCTTCACAATCTGCTACCCGGAACAACGTATGACGTTCAAGTTTACGCCCAATATGATGGCGGTGTCAGCAAACCTCTCATCGGACAAGGAACAACAT[G/A]TATGTAAAGAAACAAAGCTCGTCTGATTTCATTGGACGTATCCCATCCTCTGATTCATTTCAAACACTTCCCTCAGGATATCAGAATAGGCTTTCTTTGGCAGGGACCAACAGATTTCAATTTTCATTTGGTTTTAGTGCTATCGATCAGCTGAGTTTTAATGCATTGAAAAAGATGATGTCCGCAAAATTGTTGCAAACAATTCATTTGTGGTTAATTTAAACTAACCAATTCAATTTAGTCGAACTTGATGTTCAACTTAATTTGTTTGTTTAAATTCAGCCCAAATATATTGTTTAGTAAATCCAAGGAATCACCATAGTGTGGGAAGAGGTAGCCGCTGTTTTTAGTACTATTAATGTTGTGTAATGTTCGACGTTAGTATATTGTGTGGTATAATAACCTGATCTTTCGAGGAGATGTAACTGTTTTACATTTGGTCTGTTTCGTGGCAAATTTTTATGAATTGTACGATTTTAAAAGGAGGTGTGGCACACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12359
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Nonsense | 2857 | 3643 | 54 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49833713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49718846 |
GRCz11 | 20 | 49522406 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTSAGCCRTTCTGTGCYTCAYGRAGCTGTTTTGTGTGTGCTCAGTGTGC[A/T]AAGGAGCAAAGGCAGATGTGGTTTTCCTCATCGATGGCTCCTGGAGTATC
Long Flanking Sequence:
TGCTAAGCTGAGGTAAAAGTGCTCCCTCTAGACCTCGTGATCATCTGAATGGGTTCATTAATGGTAAAACTAAACCATTTAACTCAAGGGAATTGCTAATAGTCTAATCCCATTCAATAATCTATGCTAAGCTAAGCTAAATGGGCTCCCTCCAGATCAGAGATCATTGAAATGGATTCAGAAATGCTAAAACATAACTGTTTAACTCTAGTGGAGTAGTAAAATAAGCTTATTTTACAAAAAGAAGTGGAGTGTTATTTAAGACCTTCTGGATTAAACAAGTTTCTCATTCCTATGTATTTTCTCTAGAACGTGTGACTGATTATTGCAGTAATTACAACATGGAGGTTCATTAAGCTGCAGTTTTTTTCAGTAACTGTGTTTGCTAATGAGACTTCATTACCCTCTTCAGCTCTTGTGTAAAAGTTTCATTGTAAATGAATGGTTTGGCTTCAGCCGTTCTGTGCTTCATGGAGCTGTTTTGTGTGTGCTCAGTGTGC[A/T]AAGGAGCAAAGGCAGATGTGGTTTTCCTCATCGATGGCTCCTGGAGTATCGGAGATGAGAGTTTCAGTAAAGTCATCCAGTTCGTCTTCAGCGTTGTTGGTGCTTTTGACGTTATCGGACCAACAGGAATGCAGGTAACGTGCTAGCAATGGCATAACAACCTTAGCAGCTACAGTACTGGATTTTAAAGGTCCCGTGAAGTGCTTTGAAATGTTTGTTGGAGGTTTGACGAAATCTCAAATGTAAATTAAAGAGAGGGTGAGACATACACTCTCAGAAATAAAGGTAGGCGAGCTGTCACTGGGGTGGTACCTTTTCAAAAGGTACAAGTTTCTACATAAAAGGCCCATCCCTGCTGAAAAATCCAGCTTAAACCAGGCTAGGCTGCTGGTTGGCTGGTTTTAGCTGGTCGACCAGGCTGGTTTTAGAGGGGTTTTGGCCACTTCCAGGCTGGTCTTAGCTGGTCAGGCTGGGAGATGACCAGCTAAAACCAGCTTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6652
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Nonsense | 2988 | 3643 | 56 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49829818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49714951 |
GRCz11 | 20 | 49518511 |
KASP Assay ID:
554-5399.1 (used for ordering genotyping assays)
KASP Sequence:
TAACAGATGGACGCTCYCAGGACGACGTGCATAAGAACGCTGCCAAGTTG[C/T]AGCACGCKGGTATATATGATCCACTTYCACACGTTAAAAGATGTGACAAA
Long Flanking Sequence:
AATATACATTATCTGAAAGTTAAATAGTAAAACAATTCCTTTGGGGTATAGTTTGTTGAGCTATGATAATATTTTGTTGATAGTATTTTGTAAAAATATTTATAAATCTTTAATATAATATATAATATTATATTTAGTTAATATATATTGATATATAGTTAATAGTTTAAATGTGTATTTCATATACTGTTATATACAATATATTTTGACTATTCCCACATATATACCCACACAGCATAAGATCTTGTGGTCCAGAATCAAACTTTCTTTTTTTAATCTATTTTAAATTTCTATACATTTCATGATGAGTTGGCAGCGTGAAAGTAGATGGGTTTTGCTGATGATGTTTCCTCTGTGTTGTCGCAGGAGTGGCTCTGAAGCATGTTTATGAGAAGGTCATCACTGTAGAAAATGGGATGAGAAGAAACGTGCCCAAGGTGGTGGTGGCTGTAACAGATGGACGCTCTCAGGACGACGTGCATAAGAACGCTGCCAAGTTG[C/T]AGCACGCGGGTATATATGATCCACTTCCACACGTTAAAAGATGTGACAAAAGCGTTACTAACTTTATAGTCAATTGTAAGTCGCTTTGGACAAGAGCATCTGCTAAGTGACTAAAAATAAATGTAAATGTATATTCATCAACACCTATTTAAAAAAGTCATCTCCTGAATTGCAGTATTGTGCAGAGCTTTAACAATTATTGTACAGTTGAAGGGAAAATTACAACCCAAGCTTATTCTTGAAACGTAGCCCTGCGGACGTTTTTGGAGACCGCGATTTACGTGGCCAGAGGTACGTACGGCCGCGTTTAGTTTTTTTCGAGCGTACGCTGCGGGGTGGTGTGGCGTCGCTCCGCTCCTCCTCTTCGCGCTCGCCGGTTGACGGCTCGCCTCCGAGTGGAGGGCTTTCCCGATGCAACCAGTTTGTCCGCTTAGCTCACAGCGTTGCGTCAGCGGAGCGGAGGCCCCGGAGGAGGATGAAGAGCCTGCCGCGGGGACGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14083
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 |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 3297 | 3643 | 64 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49800960)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49686183 |
GRCz11 | 20 | 49490030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACATGCACGTCAGACAGTTCTGGACCCCCGGGCCCACAGGGGCCAGTGG[T/A]AAGTCAAATAAAGGAGGAATCTTTCTTATGGACCCTTTCACAAKACTGCT
Long Flanking Sequence:
GTGACGTCACACTTAACAAGCGGATAAGTGAATTGAATGCGCTAAATTGGCTGTAGTGTATGTGTGTGAATGCGGGTGTAAATGGGTGTTTACCAGTGCTGGGTTGTGGCTGGAAGGGCATCTGCTCTGTAAAACTAATTTTGGAATAGTTGGCGGTTCATTCCGCTATGGCGACCCCAGATAAATAAAGAGACTAAGCTGAAGGAAAATATAATGATATAGAACCTCTACATTTTTGGTTTATTTGCAGCTAAAGATATCAGTCTGGTTATGTAATTGACTTCCTTTCGATTAACTGTACCTGCTGTAAAGAATTTTTTTTTTTTTCTTCGGGATTATAAGTTCACAGTTAATTTATGGTTGCCATTTGTTCTCATGTTTTGTTGTTGTTGTTTTTCTTGATGTTATTCAGAGAGATGAATCCAAGTGTCCAGCTCTTCCCAACGCATGTACATGCACGTCAGACAGTTCTGGACCCCCGGGCCCACAGGGGCCAGTGG[T/A]AAGTCAAATAAAGGAGGAATCTTTCTTATGGACCCTTTCACAAGACTGCTATGTATATTGAGATTTTTAAAAAACTTATGAACATATATATGGGTTTACCTATGTATTATATGATCTTTGCATAAAATTACAAAAAAATAAGATAAAATAAATAAATAATAATAATAATAATAATAATAATAATAATAATAATAATAGATATTCAAGGTGTTTCCAATGCAGTGTCTTTAGGGCTTTGGTGTTGTTCTCTTCTCTGGGTGCCATCGTCAGTCTCACACAATTTTTCTCTTTTTCTGAGCGTCTTGATAACACCATCGTAGAGTTTTTCTTTTATTATTTCAGCAAATAGGATTGCAAAAAGAATGATTTGTTGTACTCTCCAATTTACTGCAAGTTTATCCAGCCATGACGCTTTCCGCTACTGAGAAACCTAGAAATGTGAAAAGAGCCCATAGAGTTCATAATATTATTGAATCCTTATTGTGTGTAATGAGTTACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19245
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 3348 | 3643 | 67 | 76 |
ENSDART00000025926 | Essential Splice Site | 3348 | 3643 | 67 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49791216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49676439 |
GRCz11 | 20 | 49480286 |
KASP Assay ID:
2261-4951.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAAAAAGTTTGGATGCTTATTTGACAGCCCCTTTTCCTTTTTTCGCAC[A/C]GGGTCGTCAAGGTCCGAAGGGGGATCCAGGCGATGCTGGCTTACCTGGAC
Long Flanking Sequence:
TGATTAGACAAGTCATCGTATAACGATAGTTTATTCCGTAGACAATTTAAATTTAAAAAACGAATATTGCTTTAGGGGGCTAGTAATATTCACCTTAAAATGTTTTTTTTTTTAAATTAAAATTGCTTTTATTCTAGCCGAAATAAAACAAATAAGACCTTCTCCAGAAGCAAAAATATTATTGGAAATACTGTGCAAATTTCCTTGCTCTGTTAAACATCGTTTAGGAAATATTCTTAATATTCGAAAAAAATCACAGGAGGGCGAAGAATTTTGACTTTAACTGTGTCTCAATTATATACCAATACCTTGGCATCCTCTATACATATACTTATTTTTTCAACTTTTTTGCTTTGTTTTTAGAGTAAGAAAATCTCTCAGATCACTCATGCCTTGTTCTCTGACTTGATATATAGTTTCAATTTTGTTTTGTTCTCATTGAAGCTCCTTATCAAAAAGTTTGGATGCTTATTTGACAGCCCCTTTTCCTTTTTTCGCAC[A/C]GGGTCGTCAAGGTCCGAAGGGGGATCCAGGCGATGCTGGCTTACCTGGACAGAAAGTAAGTGTTTCTCTGGAGAGCCGCCGAGTGTTAGAGGGAAACAGGAGGATTATTCCTCTCTCTGCTACCTCTCTGGACCCGCTCCATGTGGCAAACGTTAGATCATAACTCAGGAGGGGGGAATGCTGGGAGAACAACAGTTGTAGATCACGCCACCAGATAAAATGTAGGCTGTGGCTGTAATTTAACCCAGTTCCTAATCAGTGCCACTTAGTGGTTCTCCAATAAAATCGTTTTTGTTGGACTGTTTGGAGCTGGAGCTTCTCTGGAAAGGGAATTAAGTCATTGAGTTTTGGCTTGTAGAGGTAGCACGTACAATTTAAAAAGCCCTTAGTTGAATTTAATTTAAATAAAAAACTGAGTTAAGCTATTGTTTCAAAAGTGATTAGTTGATTTGATCTAATAAAAGTGAGAACTCTGCGGACCCGGTACCATCATCGACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10401
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025926 | Essential Splice Site | 3348 | 3643 | 67 | 76 |
ENSDART00000025926 | Essential Splice Site | 3348 | 3643 | 67 | 76 |
Genomic Location (Zv9):
Chromosome 20 (position 49791216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 49676439 |
GRCz11 | 20 | 49480286 |
KASP Assay ID:
2261-4951.1 (used for ordering genotyping assays)
KASP Sequence:
ATCAAAAAGTTTGGATGCTTATTTGACAGCCCCTTTTCCTTTYTTCGCAC[A/C]GGGTCGTCAAGGTCCGAAGGGGGATCCAGGCGATGCTGGCTTACCTGGAC
Long Flanking Sequence:
TGATTAGACAAGTCATCGTATAACGATAGTTTATTCCGTAGACAATTTAAATTTAAAAAACGAATATTGCTTTAGGGGGCTAGTAATATTCACCTTAAAATGTTTTTTTTTTTAAATTAAAATTGCTTTTATTCTAGCCGAAATAAAACAAATAAGACCTTCTCCAGAAGCAAAAATATTATTGGAAATACTGTGCAAATTTCCTTGCTCTGTTAAACATCGTTTAGGAAATATTCTTAATATTCGAAAAAAATCACAGGAGGGCGAAGAATTTTGACTTTAACTGTGTCTCAATTATATACCAATACCTTGGCATCCTCTATACATATACTTATTTTTTCAACTTTTTTGCTTTGTTTTTAGAGTAAGAAAATCTCTCAGATCACTCATGCCTTGTTCTCTGACTTGATATATAGTTTCAATTTTGTTTTGTTCTCATTGAAGCTCCTTATCAAAAAGTTTGGATGCTTATTTGACAGCCCCTTTTCCTTTTTTCGCAC[A/C]GGGTCGTCAAGGTCCGAAGGGGGATCCAGGCGATGCTGGCTTACCTGGACAGAAAGTAAGTGTTTCTCTGGAGAGCCGCCGAGTGTTAGAGGGAAACAGGAGGATTATTCCTCTCTCTGCTACCTCTCTGGACCCGCTCCATGTGGCAAACGTTAGATCATAACTCAGGAGGGGGGAATGCTGGGAGAACAACAGTTGTAGATCACGCCACCAGATAAAATGTAGGCTGTGGCTGTAATTTAACCCAGTTCCTAATCAGTGCCACTTAGTGGTTCTCCAATAAAATCGTTTTTGTTGGACTGTTTGGAGCTGGAGCTTCTCTGGAAAGGGAATTAAGTCATTGAGTTTTGGCTTGTAGAGGTAGCACGTACAATTTAAAAAGCCCTTAGTTGAATTTAATTTAAATAAAAAACTGAGTTAAGCTATTGTTTCAAAAGTGATTAGTTGATTTGATCTAATAAAAGTGAGAACTCTGCGGACCCGGTACCATCATCGACTTT
Associated Phenotype:
Not determined