ZMP
syne2a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate spectrin repeat containing, nuclear envelope 2 (SYNE2) [Source:U
Human Orthologue:
SYNE2
Human Description:
spectrin repeat containing, nuclear envelope 2 [Source:HGNC Symbol;Acc:17084]
Mouse Orthologue:
Syne2
Mouse Description:
synaptic nuclear envelope 2 Gene [Source:MGI Symbol;Acc:MGI:2449316]
Alleles
There are 38 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45694 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29341 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa752 | Nonsense | Available for shipment | Available now |
sa12747 | Nonsense | Available for shipment | Available now |
sa37016 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37015 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43424 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23681 | Nonsense | Available for shipment | Available now |
sa43423 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10833 | Nonsense | Available for shipment | Available now |
sa43422 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23680 | Nonsense | Available for shipment | Available now |
sa11385 | Nonsense | Available for shipment | Available now |
sa10113 | Nonsense | Available for shipment | Available now |
sa32287 | Nonsense | Available for shipment | Available now |
sa17499 | Essential Splice Site | Available for shipment | Available now |
sa23679 | Nonsense | Available for shipment | Available now |
sa9101 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37014 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43421 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43420 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37013 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37012 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23678 | Nonsense | Available for shipment | Available now |
sa13943 | Essential Splice Site | Available for shipment | Available now |
sa23677 | Nonsense | Available for shipment | Available now |
sa23676 | Nonsense | Available for shipment | Available now |
sa37011 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11511 | Nonsense | Available for shipment | Available now |
sa43419 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa5949 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15833 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45694
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 29 | 8864 | 1 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 21868249)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21896416 |
GRCz11 | 20 | 21796089 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATGAGAGGGGCGTTCTACTGGACATTGATGACGTTCACTTGCTTTTA[C/T]AAGGTTAGTCTTAACTTTCAGAAAATTATCGGTCTTTGTTTATTTAGTTC
Long Flanking Sequence:
AACAGACCACAGCATTACAAGTTAACTTTCTGATCAAAATCTGACTTGCCAATCAGAGTAGACCATTCTTAACCTGCCCTTATTAGAGGTCTGTGACAAAATAGTCAATCAAAACGTGCATAAAGCTAAAGCTAAACCACATTTCTAATGCATGATGTGCTAAAAAGAATAAAGAAAATGTTAACTTTCTTCTTTCATATTTTGCTATTTTCTGCAAAAGTACATTTATATTTCAAAAGTTGATTTATTTTTTTTTCTTAATTTACATAGATTTTATTTACAATATAACTCTCTATACAGAGAGTCTGCAAGAGCTCAGAAGATAAAAATGTGAATTCTTTCCATCTTGTCATATTTTTTATTTTAATTTGATCATTTCAGGGGGAATGAGTTTGTGATAGTGTCGAGTCAACAGTATGGCGTCAGGGGAAGAAAGCAGTGCTCCTCCTGAGGATGAGAGGGGCGTTCTACTGGACATTGATGACGTTCACTTGCTTTTA[C/T]AAGGTTAGTCTTAACTTTCAGAAAATTATCGGTCTTTGTTTATTTAGTTCTATTTGTGTGGCCTTGAGCATTTTTCAGTGAGCATATTTTTAGAATATTATTAAACATTGTTTCCTTAATCTGAATGGTTTAAAATTTGCACTTTGTGTACACCTTTTTAAGATGTATTTTGTATCAATAACAATTGGGTGACATAAAAGATGTAAATGGGCTCTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTATTTTTTTAATTTTTTAATTTTTTAATTTAGTATTTTTTTTTCATTTAAGATTTAATTTAATACATTTTTTTATTTAAGGTTTAATTTAATATTTTTTTCATTTAGCTTTTAATTGAATTTTCATTTAAATTATTTAATAAAGTAAATAAATAAATAAATATACATACATACATGCATATATATGTATATGTATATATATATATATATATATATATATATATATATGTGTATATATATATGTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29341
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 615 | 8864 | 15 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21842666)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21870833 |
GRCz11 | 20 | 21770506 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTATGGAGCGTGTGCTGGGTGCATGGGAGTCCTACAAAGACTACCTGTA[T/A]CGGTTACAGGTCTGGCTGGGGCAGGAGAGTCAAACACAGATGCAAGAGAA
Long Flanking Sequence:
AAAGATATATTGAGTTTGTGTTAACCACACACCCTATATCAACCAAAAACACATTTAAAAGTCCATTGACGGTAAAGTTTTTTATTTTTTATTTATTTTTTTACTTTTCTCTTTAACACTACACTGTTACTCTAATTCAATCTTTTAACTATTAAATAATGTATATATCTTCAACTAGGAAACTGTTGACAAGGAAGGCCTGGTGTGGAAGTTGAAGGAAGCTCTACATAAGCTGAAAGACACAACAATCAGTTATGCAAGCAAAGCAGCCCTGGGTAAGTTTGTATTAAATCCATTAATAAAAGTCATTGGCTTCTTCCTATTACTTCTATCTGATTTGCTCTTTCTGTTTCTTTTGCAGCGGACGACTTGCCTGTGGTAAACAGGCAGGTAAAGGAAGCTGATAGTGAAACAAGAGCCATCACTGATGCTGCAGAATCAGTCAAGTCTACTATGGAGCGTGTGCTGGGTGCATGGGAGTCCTACAAAGACTACCTGTA[T/A]CGGTTACAGGTCTGGCTGGGGCAGGAGAGTCAAACACAGATGCAAGAGAAAGAGGTACAATACAGCATTTGATAACTGACATTATCAAATGCTGGTGTCTTGTTATTTTATTAGAAAATCTTATTTCATTAGTTATTATAATATCAGAATAGTGATCATCTTTTTTTAGTCTCTTCAGGATTTTGCAGGACATTTTTCAGATTCCTACTAAAAGGATTGCAGTGAAAATTTGCAAAAACATTTTTTTATTTTTGTGCCGTTAAAATGAAGTAAACACTGAGAAAACAAAAACAGAAACTAATGTCTACCCTGTAAGAGCCATTTAATATCATTTATTATTAGAGCTCAAATTCATCTACAATTTAAACATGTTGATATGTTTAATTGTGTACATTGTTGATTTCACCACTGCTCCTTTGTTTGTAATGGTTTGCTCTGCCCTTAATGGACTGTTTTAAGTTACATTACAAAATGGGAAAATGAAAAGAACGAAAGAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa752
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 819 | 8864 | 19 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 21838470)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21866637 |
GRCz11 | 20 | 21766310 |
KASP Assay ID:
554-0659.1 (used for ordering genotyping assays)
KASP Sequence:
GGAGCACAGAGGCCCAAGAGGTCTGCCAGCACCTAAGCAGCAGGCAGCGT[C/T]GRGGCCACTTGGAGCCACATCTTAGGGCTAAAGTGAGTAGAAATTGGCTT
Long Flanking Sequence:
GAAATTAAAAGTCATATATCAGTCATGTCTGTGAAAGAAATAAACAGTTTTTTTTTTTTTTTACTGAATCAAGTCTGTAGACTGATTCATTTGCATTTGTAGATATCAATTTAATTTATTAAGACTGTCAGTAAATTGTGTTCCTGTATTTTGTGTTAGTAGTAGGTACACTGACTCCAATGTTAAGGTGTGTTGTCAGTATTTCATTTTTATTTGGTTTCTCTCTATAGAAGTTCTATCCTGACACCCCCAATCTGGAACCCTTATCTTTTTCTTGGATGAACTACTTTTCTTAAATATTGTGTGATGCTAATGCGAGTAATTGATGACTAAATATGTGCTCTTTTTTTGGCCAGATGTATAACACTTTAAACCGAGTAGATCAGGTGTGTGAGGGGCTCCAGAGAGCGGCGTCTCTTCTTGAAGGCAGATTAGCTGAGCTTGAAAACTGGAGCACAGAGGCCCAAGAGGTCTGCCAGCACCTAAGCAGCAGGCAGCGT[C/T]GAGGCCACTTGGAGCCACATCTTAGGGCTAAAGTGAGTAGAAATTGGCTTTGATTGGCATAGTTAATTTGGATACTTAAAGCAGAGCTTTCAAACTGTCATCCCTGTTGATTCCTGTTGCAGGCTTTGATATCTAGAGGTCTACAGTTGGAAGGACAGGTGGTGACAGAGGGCGAGGACCTGCAAGTTCTCGTGACATCTTTGCAAAAGAACTTCACCCTGCCTTACCTCAGCATAACAGACCTTCAAGACCGACTGAAGCAGACAGTCTCTCTCTGCCAGGTGTGTTTCATTACAGAGCAGGTTCTGTGGAGGAAGTTGAAAGTTTTATAACATCTCGCATCTTTTTGTATGTCTGTCAGGAGGTTACTGAGATGCTCAGTTGTCATGGAGTAAAGCGTGAAGGACAGCCTGAAAGTGCACGGCCTGCTTCCAAGGTTTTTGTGCATACACTTTCTCAGCCTGAATTTCAAACTGGAAGCATTCAGCACTATCAGATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12747
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 988 | 8864 | 21 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 21837793)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21865960 |
GRCz11 | 20 | 21765633 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCATGATAAATCTCCCGAAGATCAAAGGAAAGCTAAATGCCAAATACAG[C/T]AAGCAGACCTCAAACAGCCTTTGTTGTCATCCGTTGTTGGCAGGAAGGTT
Long Flanking Sequence:
GACCTGCAAGTTCTCGTGACATCTTTGCAAAAGAACTTCACCCTGCCTTACCTCAGCATAACAGACCTTCAAGACCGACTGAAGCAGACAGTCTCTCTCTGCCAGGTGTGTTTCATTACAGAGCAGGTTCTGTGGAGGAAGTTGAAAGTTTTATAACATCTCGCATCTTTTTGTATGTCTGTCAGGAGGTTACTGAGATGCTCAGTTGTCATGGAGTAAAGCGTGAAGGACAGCCTGAAAGTGCACGGCCTGCTTCCAAGGTTTTTGTGCATACACTTTCTCAGCCTGAATTTCAAACTGGAAGCATTCAGCACTATCAGATGTTCTCTCGAAGCAGCAAACTTTCCTTAGACAGCCCAGTGGAATCTCAAAAACAAGACTTTCATTCCTTTCAGCTGCAGACACCATTTGAAGCCACTGGTGGTGCAAAGCACCAGGCCCTCAGTCAGTTTCATGATAAATCTCCCGAAGATCAAAGGAAAGCTAAATGCCAAATACAG[C/T]AAGCAGACCTCAAACAGCCTTTGTTGTCATCCGTTGTTGGCAGGAAGGTTCAAATGAAACCCCAGACTAAAGTTCATCTTATCTCTGTAGACTCGAGCCAAACCTCGTGCCCTGGATCCTCAGGACCTTTTCAGGTTATCTCTGTAGAGTCAAACCAATCCAGCAGCATTGAACCCTCAGTCCCTCTCCCAGTTGTTTCTGTAGATTCAAGCCATACAAGGGGCTTTAGACCATCAGAAGTTCAGGTTGTCTCTGTAAACACAAGCCAGACCATTAGCTTTGGACACTCAGACACTCTCCATAGTATCCCTATTGAGTCAAAACAAACCAGTGGCTTTGGAGCATCAAGCCCTCTCCAAGAAATTTCTGTACACTCAAGTCAAGCCAGTAGCTTTAGACAATCAGAACCTCACGTTTTCAGTGTAAACTCAAGTCAGATGAGTGGCTTTCCACCCTCAAACCGTCTTTGGGTTAGCTCTGTAGGATCAAACCAAACCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37016
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 1213 | 8864 | 21 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21837118)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21865285 |
GRCz11 | 20 | 21764958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCTCTCCAGGTGGTTTCTGTAGACTTAAGCCAAACAAGTGGCTTTAGA[C/T]AATCAGAGGTACAGGTTGTTCATGTAAACACAAGCCCGACCATTGGCTTT
Long Flanking Sequence:
CCTCAGTCCCTCTCCCAGTTGTTTCTGTAGATTCAAGCCATACAAGGGGCTTTAGACCATCAGAAGTTCAGGTTGTCTCTGTAAACACAAGCCAGACCATTAGCTTTGGACACTCAGACACTCTCCATAGTATCCCTATTGAGTCAAAACAAACCAGTGGCTTTGGAGCATCAAGCCCTCTCCAAGAAATTTCTGTACACTCAAGTCAAGCCAGTAGCTTTAGACAATCAGAACCTCACGTTTTCAGTGTAAACTCAAGTCAGATGAGTGGCTTTCCACCCTCAAACCGTCTTTGGGTTAGCTCTGTAGGATCAAACCAAACCACTGGCCTTCAATCCTCAGACCCTTTACAGGTTATGTCTGTTGAGTCAAGCCAATCTAGCAACATTGGATCCTCAGAACATCTTCATGTTACCTCTGTAGAATCACAACAATGCAGTGAGCCCTCGGACCCTCTCCAGGTGGTTTCTGTAGACTTAAGCCAAACAAGTGGCTTTAGA[C/T]AATCAGAGGTACAGGTTGTTCATGTAAACACAAGCCCGACCATTGGCTTTGGACTCTCAGATCCACTTCAGATTATACCTGTAGAGTCAAACCAAATGGGTGGCTTTGGACCAATGGACCTTCAAGTTGTATCTACAGACTCAAGACAATCTACTGAGCCATCAGTTTCATCCAGCACTATGTCCAGCACAAGCACTTTGATTAAATCAGATACCATGACTCCACTAAGAATGCCAATTGAACAGCACCTAGCTTCACCACCAACACGCCAAGTTCAAACCTTATTAGCACCCTCGAAGCAAAGACAAACTGTTCTAGTCAAAAGTTGCAGCTTTACCCAGCCCCATGATGAGCAATCGCAAACCCAGTCTGCTTCCTGCCAAAGCACTTTAGGTGAAGCGGTCACAGTGACTCGGCTAAGAACCCCAATTAAACACTTCTTTGATTCACCACCAAAATTGCAATCTCAGACCTCAGTGACAACTTTACACCCAAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37015
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 1315 | 8864 | 21 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21836812)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21864979 |
GRCz11 | 20 | 21764652 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCACCAACACGCCAAGTTCAAACCTTATTAGCACCCTCGAAGCAAAGA[C/T]AAACTGTTCTAGTCAAAAGTTGCAGCTTTACCCAGCCCCATGATGAGCAA
Long Flanking Sequence:
TAGGATCAAACCAAACCACTGGCCTTCAATCCTCAGACCCTTTACAGGTTATGTCTGTTGAGTCAAGCCAATCTAGCAACATTGGATCCTCAGAACATCTTCATGTTACCTCTGTAGAATCACAACAATGCAGTGAGCCCTCGGACCCTCTCCAGGTGGTTTCTGTAGACTTAAGCCAAACAAGTGGCTTTAGACAATCAGAGGTACAGGTTGTTCATGTAAACACAAGCCCGACCATTGGCTTTGGACTCTCAGATCCACTTCAGATTATACCTGTAGAGTCAAACCAAATGGGTGGCTTTGGACCAATGGACCTTCAAGTTGTATCTACAGACTCAAGACAATCTACTGAGCCATCAGTTTCATCCAGCACTATGTCCAGCACAAGCACTTTGATTAAATCAGATACCATGACTCCACTAAGAATGCCAATTGAACAGCACCTAGCTTCACCACCAACACGCCAAGTTCAAACCTTATTAGCACCCTCGAAGCAAAGA[C/T]AAACTGTTCTAGTCAAAAGTTGCAGCTTTACCCAGCCCCATGATGAGCAATCGCAAACCCAGTCTGCTTCCTGCCAAAGCACTTTAGGTGAAGCGGTCACAGTGACTCGGCTAAGAACCCCAATTAAACACTTCTTTGATTCACCACCAAAATTGCAATCTCAGACCTCAGTGACAACTTTACACCCAAAACAAAGGGTTTTAGCAAGAAGTCACAGCTTTCCACAACAAGTACAGGCTTCAGGCGTTCCTCATATCCCAGTTCAGAATGAGGTGTTTGCCAGAGCTCAGGCTTTAGCCAGGAGCAGACTGGAGAAAGCCAAAAATCACCTGGATGAACACATACAGGATGTGATTACTGTGATCCGTACCAGAGACAAATCTAAAAAACAAGGCAAGAAAAGACAGGTGAGACAAACTTGTAAAATAATGGTTTCTAAAAATATTAAATAGTCAGCCAAAACACATACTGTAAATTATTAACAACTTTTTGCTATTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43424
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 1852 | 8864 | 29 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21825002)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21853169 |
GRCz11 | 20 | 21752842 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCAGCTGAACGATGAATTAAATGCTCACAGGACGTCAGACCAAAGCTA[C/A]AGTTCAGTGTCCTTCCAGAAAAGCCTTGAACAGGTCAGGGAAGATTCGCT
Long Flanking Sequence:
CTAACTCACCTTTCACTTTTTTCTTCTACTTGTTGAACGCGAAAGAAGATATTTTGAAGAAAGATAGAAACCTGTAACCATTGACTACCATAGTATTTGTTTTGTTGGGTAAACTATGCCTCTAAGATACGTTTGCTCCCTCATTCAAATTTAGCTGTAATGTATTTTTCATGAACTGATGTACTTTGCATTTTTGAACGTACTTACAACCTGACATCTTTGTTCTTTATATAGTGTGTGGATGAAAGTATCAAGAAAGAGCTGTTTCTTCTTAACGAGAGAGAAAGTTTAGTAGGGGATGGCACTGATCTGAGTCACATTGAGCTTCAAACTCATCTTCCTCTTCAACAAACTCTCCACAACCGCACAAAATGCCTGGAGCAGCAAAGACATTGTGTGCAAAAGTCTGAGTCGGCTCTTGTGGCCCTCGAGAAGCTTCTTTCTCATCTCCAGCAGCTGAACGATGAATTAAATGCTCACAGGACGTCAGACCAAAGCTA[C/A]AGTTCAGTGTCCTTCCAGAAAAGCCTTGAACAGGTCAGGGAAGATTCGCTTCAGCTGGACACAATGCTGGATGATGCTGGTCTAAGGATCACACTGGATGATAAAGCAGGCAGCTGTGTTGAGATGGTGTCAGCGCTGGAGGAGGGGTTCCAGGTCAGACTCGTTGAAGGACAGAGAGTGTCTGATGGAGGGCGGAAGGGAAGAGAGAAGCAGGAGAAGAAGGAGGAGAGAGCGTTTGGGAGGAAGAGGATGGGTCTGTTGGTCACATTGAGGGAGGTGCTGGCAGCACTGGAGAGACATGTGCTGAAGGAGCCCACACTTCCTGCTCTACAGCACAGGTGAGGAGACTCAAAAACAAGAGATAGTTAACTTAGTTAACTTTATGTATTTATTTATTTTATTTTAAAATTTCATTTCATTTCATTTTCATTTTCTCTTCGGTTTAGTCCCTTTATAAATCTGGGGTCGCAACAGCGGAATGAACTGCCAACTTATCCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23681
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 1862 | 8864 | 29 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21824974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21853141 |
GRCz11 | 20 | 21752814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGGACGTCAGACCAAAGCTACAGTTCAGTGTCCTTCCAGAAAAGCCTT[G/T]AACAGGTCAGGGAAGATTCGCTTCAGCTGGACACAATGCTGGATGATGCT
Long Flanking Sequence:
CTTGTTGAACGCGAAAGAAGATATTTTGAAGAAAGATAGAAACCTGTAACCATTGACTACCATAGTATTTGTTTTGTTGGGTAAACTATGCCTCTAAGATACGTTTGCTCCCTCATTCAAATTTAGCTGTAATGTATTTTTCATGAACTGATGTACTTTGCATTTTTGAACGTACTTACAACCTGACATCTTTGTTCTTTATATAGTGTGTGGATGAAAGTATCAAGAAAGAGCTGTTTCTTCTTAACGAGAGAGAAAGTTTAGTAGGGGATGGCACTGATCTGAGTCACATTGAGCTTCAAACTCATCTTCCTCTTCAACAAACTCTCCACAACCGCACAAAATGCCTGGAGCAGCAAAGACATTGTGTGCAAAAGTCTGAGTCGGCTCTTGTGGCCCTCGAGAAGCTTCTTTCTCATCTCCAGCAGCTGAACGATGAATTAAATGCTCACAGGACGTCAGACCAAAGCTACAGTTCAGTGTCCTTCCAGAAAAGCCTT[G/T]AACAGGTCAGGGAAGATTCGCTTCAGCTGGACACAATGCTGGATGATGCTGGTCTAAGGATCACACTGGATGATAAAGCAGGCAGCTGTGTTGAGATGGTGTCAGCGCTGGAGGAGGGGTTCCAGGTCAGACTCGTTGAAGGACAGAGAGTGTCTGATGGAGGGCGGAAGGGAAGAGAGAAGCAGGAGAAGAAGGAGGAGAGAGCGTTTGGGAGGAAGAGGATGGGTCTGTTGGTCACATTGAGGGAGGTGCTGGCAGCACTGGAGAGACATGTGCTGAAGGAGCCCACACTTCCTGCTCTACAGCACAGGTGAGGAGACTCAAAAACAAGAGATAGTTAACTTAGTTAACTTTATGTATTTATTTATTTTATTTTAAAATTTCATTTCATTTCATTTTCATTTTCTCTTCGGTTTAGTCCCTTTATAAATCTGGGGTCGCAACAGCGGAATGAACTGCCAACTTATCCAGCACGTTATACACAGTGGAAGCCCTTCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43423
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 2333 | 8864 | 36 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21815579)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21843746 |
GRCz11 | 20 | 21743419 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAAGAAAGCATTAGAATTGCCAAAGAGCTTAATATAAAGAAGGGAGAA[C/T]AAACAATGAACCCAAACAAGCCTGTAACTTCTCAGCCTGTCGAAGAGTCT
Long Flanking Sequence:
TATGGTGTGTTGTTTTTGATGGGCATGTAGCATTTAAGACAAGACACTGTGATTCACACCAATAACTAAATGATCCATGTGTTGCAACCAAGCAGTGCTGTTTAGCTCTGCTTTGAAGCATAAACATATTGAAAATGTTGTAATTTTATGAAAGGAAAATTATTGTTACCCTTTAATCATCAGGCACTGGTGTGTACATTAGATGCCTATTTTGATGTGCATGTATCCAATGGCTCTGTCACATTGTTTAGTTCATACTTTAGTTCACCCATATTTTTATTTTTTGTGATGGACTAATCCTTTAATGTAACTGTTTTGACTGACAGAGATTATCGGAGCAGCTGGAAGTGAAGGCTGAGCAGGCAGATGCGTTACTGCAGCAGATGGATCTCCTTGCCAGCATTGCAGGTCTGGAAAACCTGCAGACTCTTTCTGAAGCTGGTGCTCACCTTCAAGAAAGCATTAGAATTGCCAAAGAGCTTAATATAAAGAAGGGAGAA[C/T]AAACAATGAACCCAAACAAGCCTGTAACTTCTCAGCCTGTCGAAGAGTCTAAGCATACCGAGGCCCATATTGAAAAAGTAGAAGATACCACAGAGTTACAGACTGTATGGGATGATAAAGCAGATGAACAGTCACAGAGAAGCAAGGCAAAAGATGCGGCTCTTGAGCAGAAGTACTTTAAAGAGGATATTCTTCTGTCTGAGGATGAGAACTGGCGGGTCACACCTAAAGAGAGACTCACATATGCACAGGTTAGTTTCTTTTCTTTTATATGTTTGTTCTGTGCCTTTAAAGTGACCTGAACTGAAATACAAAGGAGTCTGGTTGGAAATCATTTTAGTTTAAGAACTAGGATCAATTTGTTTCTTGGAAACAGCTGTAATGAGAGTTTTGTCTGTTAACAGCAATTTAAATTCCATTCCAGTTCCATCATGCTGCAAAAAGTACCTTTGACGCACTAAAGGAAATGTAGTTTTGATATGAAATGTGGGGGGAAAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10833
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 3034 | 8864 | 37 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21808217)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21836384 |
GRCz11 | 20 | 21736057 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTTGCTAAARGTAGKAAAAAGAWCAAGAAATCAGTTGATGCAGTGAAA[A/T]ARGACAATATCAGTAGYTTAAAGCTGAAGGCTTCCACATCTGAACATAAA
Long Flanking Sequence:
CCATTGTAGATGTTAATTCAACAACATTGTTGTCAGACAGTCATCAGTCACTGTTGCAGACACAACACACAGGTCTTAAAGACTCAAAAACAAAAGAATTTGCCTATAAAGATGCCAAAACTCAACAGAGGAGCTCTGCTGGCACAGTGGAACCTGAAGAACAAGAGCCTGAAAGATTGCTTTCAAAGAAATACAATGTGAAATCACTTAGCTCTGTATTACAGGAAGCTCTCCAGCCCAACACCTCTGAGATCATGGAGACTGACATTGAAAAACGTGACAAAGAGAAGCAGCACAAAGTCACTGATGCTGAAACATCAAGTCAAATAGGCGCCTGTGCTGAAGACAATGAATCAGGGATCAAAACACTTAAGCAGGATGTCACAATGTCAGACAAACACACATTTGCAGAACCCTCAAATGATGCAAACGCACTTCAAAAACCTCCAAATGTTGCTAAAGGTAGGAAAAAGATCAAGAAATCAGTTGATGCAGTGAAA[A/T]AAGACAATATCAGTAGTTTAAAGCTGAAGGCTTCCACATCTGAACATAAAACCAAAGCTGAGTTAGAAAGTCTTCAAACTTCTGAGATGAAAGTACCGGACACTACAGATACTTCACTGAATGTGGCTTCAACCTGTAGTCAGTCAAAGAGGACTGAAGACAAACACACAGAAGCTGTGGGCACTGTGCAAGAAGATGGGTTAAATCTCCTGCAGACTGAGGCAAAGCATGGTCTTTTTGGTACTGTTGCAGTTTCAGTTGTCGGAGGTGCTCCTATTGAAGCCACAGACATTGGTTTAGAAACAGCAGACATTGTGCAGTCAAAACACACAGAGAAATCAATGGCAGCAGATGCATTACCAGTCATGAGAGCTGAAGGTATTACACAGATTCCTGCTGTCGTTGTGAATGTTAAATCTCCAACGTTCAGTCATCAGCCACTGTTGCAGACACAATGTACAGATTATAAAGACACAAGAGCAGATGTATTTGCCCATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43422
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 3802 | 8864 | 37 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21805913)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21834080 |
GRCz11 | 20 | 21733753 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTGAATGTGCTCCTATTGAAGCCACAGAGAGTGTGGTTTTAAAAACA[G/T]AAGACAGTGTACAGTCAAAACATGCAGAGAAATCAATGCCAACAGATGCT
Long Flanking Sequence:
GTGTACTAATGGTAGAAGGCAGTAAATGTGGGTTTGTAGTACACAAGCAGGATAAAACAATGTCAGAGAGTCATGGTGAGGCTGATAAAATCACATTTGCAGAGCCCTCAAGTGAAGCAAACACACTTCAGAAACTTACAAATATTGCTAAAGGTAGGAAAAAGATCAGTAAATCAGCTCTTGCAGAGAAATCAAACAAAACCACAAATAGAAATCAGAAGACATCTAGATCTGAACATAATAGTACAGCTGATTCAGAAAGCCTTCAAACTTCTGAGATCATACTGCCAGACACTACTGATACTTCACTGAATGTGTCTTCAACCTGTAGTCAGTCAAAGACCACAAAGTCAGTGAGTTCAGAAGACAAACTCTCTGAGACTGTGGACACAGAGACTTTAAATCTCCTGCAGACTGAAGCTAAGCTTGGACAATTTGGTACTGTTGGAGTTGTTGAATGTGCTCCTATTGAAGCCACAGAGAGTGTGGTTTTAAAAACA[G/T]AAGACAGTGTACAGTCAAAACATGCAGAGAAATCAATGCCAACAGATGCTTCGCAAGTCATGAGAGCTGAACATATTACACAGATTCCTGCTGTCATTGTAGATGTCGATTCACCACCATTATTATTATCAGGCAGTCATCAGTCACTGTTGCAGGCACAATGTACAGATTCTAAAGGCTCAAGAGAAGACATAAATGCCTATAAAGATGCCAAAACTCAACAGAGGAGCTCTGCTGGCACAGAGAAACCTGAAGAACAAGAGCCTAAAGGTTTGCTTTTAGAGAAGTACAATGTGAAATCAAGTTGCTTAGTAATACATGAAGCTTTCCATCCCAACACTTCTGAGATCATGGAGACTGACATTGAAAAATGTGAAAAAGTGAAGCAACATGTAGTCACTGATGCTGAAACATCAAGTCATATGGATGCCCGTGCTGAAGACAATAGATCAGGGATTAAAACACTTCAGCAGGGAGTCACAATGTCTGAGAAACAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23680
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 3876 | 8864 | 37 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21805691)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21833858 |
GRCz11 | 20 | 21733531 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAAGGCTCAAGAGAAGACATAAATGCCTATAAAGATGCCAAAACTCAA[C/T]AGAGGAGCTCTGCTGGCACAGAGAAACCTGAAGAACAAGAGCCTAAAGGT
Long Flanking Sequence:
CATCTAGATCTGAACATAATAGTACAGCTGATTCAGAAAGCCTTCAAACTTCTGAGATCATACTGCCAGACACTACTGATACTTCACTGAATGTGTCTTCAACCTGTAGTCAGTCAAAGACCACAAAGTCAGTGAGTTCAGAAGACAAACTCTCTGAGACTGTGGACACAGAGACTTTAAATCTCCTGCAGACTGAAGCTAAGCTTGGACAATTTGGTACTGTTGGAGTTGTTGAATGTGCTCCTATTGAAGCCACAGAGAGTGTGGTTTTAAAAACAGAAGACAGTGTACAGTCAAAACATGCAGAGAAATCAATGCCAACAGATGCTTCGCAAGTCATGAGAGCTGAACATATTACACAGATTCCTGCTGTCATTGTAGATGTCGATTCACCACCATTATTATTATCAGGCAGTCATCAGTCACTGTTGCAGGCACAATGTACAGATTCTAAAGGCTCAAGAGAAGACATAAATGCCTATAAAGATGCCAAAACTCAA[C/T]AGAGGAGCTCTGCTGGCACAGAGAAACCTGAAGAACAAGAGCCTAAAGGTTTGCTTTTAGAGAAGTACAATGTGAAATCAAGTTGCTTAGTAATACATGAAGCTTTCCATCCCAACACTTCTGAGATCATGGAGACTGACATTGAAAAATGTGAAAAAGTGAAGCAACATGTAGTCACTGATGCTGAAACATCAAGTCATATGGATGCCCGTGCTGAAGACAATAGATCAGGGATTAAAACACTTCAGCAGGGAGTCACAATGTCTGAGAAACAAACATCTGGAGAGCCTTCAAATGAAGCAAATGCACATCAGAAATCTCCAAATGTTGCTAAATGTAGGAAAAAGATCAAGAAATCAGCTGATGCAGAGAAATCAGACAGTACCAGTAGTGTAAAGCTAACATCCCAGCATAAAAGGACAGCTGATTCAGAAAGTCTTCAAACTTCTGAGATCATAGTGCCAGACACTACAGATATTTCATTGAACGTGTTTTCAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11385
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 4382 | 8864 | 37 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21804173)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21832340 |
GRCz11 | 20 | 21732013 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGATATTTTGGGGCTGTTRGAGTTTCAGTGGTTGGAGGTGCTCATRTT[G/T]AAGYCACAGATAGTGTGGYTTTAGSAACARGAGACATTGTGCAGTCAAAA
Long Flanking Sequence:
AGCATGTAGTCACTGATGCTGAAACATCAAGTCATATAGATGCCCGTGCTGAAGACAATAGACTAGGGATTAAAACACTTAAGCAGGAAATCACAATTTCTGAGATACAAACATCTGCAGAGCCTTCAAATGAAGCAAATGTACATCAGAAAACTCAAAATGATGGTAAAGGTAGGAAAAAGATCAGGAAATCAGCTGATGCAGAAAAATCAGACAATATCAGTACTATAAAGCTGGTATCCAGATCTGAAAATAAAAGCACAACTGATTCAAAAAGTCTTCAAACTTCTGAGATCATACTGCCGGTCACTACTGATACTTCACTGAATGTGTCTTCAACCTGTAGTCAGTCAAGGACCACAAAGTCAGTGATTTCAGAAGAAAAACTCACAGAAGCTTTGAACACTGTGCAAGAAGAGACTTTACATCTCCTGCAAACTGAGGCAAGGGATGGATATTTTGGGGCTGTTGGAGTTTCAGTGGTTGGAGGTGCTCATGTT[G/T]AAGCCACAGATAGTGTGGTTTTAGGAACAAGAGACATTGTGCAGTCAAAACACACAGAGAAATCAGCGCCAACAGAAGCTTCACCAGTCTTGAGAGCTGAATGTATTACACAAATTCCTGCTGTCATTGTAGATGTCGATTCACCAACATTATTATCAGAGAGTTATCAGTCACTGTTGCATACACAATGTACAGGTCCTAAAAGCTCAAAAACAGAAGAGTTTTCCTATACAGATGTCAGAAATCAATGGAGGAGCTCTGCTGGCACAGAGGGACCTGAAAAACAAAAGCCTGAAAGATTGCTTTCAGAAAATGACAATGTGAACTCGAGTTGCTCTGAAATAAAGGAAGCTCTCCATCCCAAAACCTCTGAGATCAGGGAGACTGGCATTGAAAAAAGTGAAAAAGAGAAGCATCATGAAGTCACTGATGCTGAAAGATCAAGTCATATGGACACCTGTTCTGAAGACAATGAATCAGGGATTAAAACACTTAAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10113
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 5074 | 8864 | 41 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21797924)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21826091 |
GRCz11 | 20 | 21725764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGAGCTGCAGATCKGGCAGTGTTAACAGAGCGCTGCTTGTACCTGCAT[G/T]AGGTCTCTCAAGCTCTTTTTTCAAKTCCACTGGRAAAGAAAGAGATCAGA
Long Flanking Sequence:
AAGAGTTTTTGTTCAGAGACTCTAAGAATAATACTTAATATCATGCCAGAAAAGTAACCACATTATTCTCCTGATTTTAAAGGGGTTGTATTGAAAGCAGCACCCTGCAAGCAGAAAAGCTAAACGCATTCCTGAAGAACATGCAGAAGAATAGAGGCATGCTTGAGGATCTTCTACAGACTTGCTCTCAGATCTCAGCCCATCTTGGTGAGGCAGAGGGACATGTGGCCTGTATTGAACCTGTCAGGACCTGTCAGGAAAGATGGCAGACTCTAGAGCAGACCGCTTTCAGGAGTCTGTGGTGCGCTAACATATGCACAACAGAAGCTTCCGCACTCCTTCAAGAGTCCAGAGAGCTGCAGTTTGAAATGGAGCTTCTTGTGAAGTCAGTTTCCTCTGGCCACCTCTCTCAAGGACAGATTGATTGGCAAAATGCAATACGGGACACCATGAGAGCTGCAGATCTGGCAGTGTTAACAGAGCGCTGCTTGTACCTGCAT[G/T]AGGTCTCTCAAGCTCTTTTTTCAAGTCCACTGGGAAAGAAAGAGATCAGAGATGTAGAAGACACAATCCAGGCTCTGAATTCTCAACTTGAACTGACTAAGGAGAAGATTGGCTGCCAGACTCCAAATAGCAGTGATCATTCAGCTGTAGTGAGGATTATTAGGGACTATGTTACATGGGCCAAACAAATGGAAAGCAGAATCAGCAGGAGAAGGAGGATGTCTCTATTTCCAGAAGAGGCAAGTCATCAAGTCAACCACATGAAGAAATTGCAGTCTGAAACATCTCTTAAGAGGTTTCAGTTGGCCTCTGTTTTGAAAGAAATTAGAGAAGAGGTTACTGAGCTTGACGAGGAAGAGTCTAAAGCCATGCTGTCCACCTTCGATTCCTTGGAGGAGCTGTATAATAACACTGCAAAAAAGACTGAATCTGCCCTTGAAGAAATGAATAGAACGTTGCTTATTAGAGATAGACTGTGGAAACAGATCACAGACAGCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32287
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 5667 | 8864 | 42 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21794014)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21822181 |
GRCz11 | 20 | 21721854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCTCCACTGGCTTTAAAAATGACCGAGAGGAGCTCCGCTATATTCAA[C/T]AGATCTTCAGCTCTCTTGCTGAGGGTTTCCAGGCCCGTTTGTCAGAAATT
Long Flanking Sequence:
TATGACAAAAACATTTTACAACACATGCAAAGGTAAAAGAGTTCAGAACTAGACAGTACCCATAACCTTAGCTATTTACCCACCTTTTCACATTCTCAGTATGCCATATCCAACTGTATTTACGTGAGACAGTCCTCGAGGTACATTTTGACAACCATTTGTATCAGTACTGTAGTTACATTCCCAACTATACAGTTATCTCCCAACGTATGCAGTTGAGAAAATTAGTTGATAATAATATCTGTAGGAGGGAAAGTGCCATACAATGCATTTCTGTTTTGGGGAAAAGCATACATCAATTTTTGTAAAACTCAACATTATTAATGCTTTTTCTGATATTTTGTTTGATCCAGGACAAGCTGCTCCAAGCTCAGGAGGCATTAAAGCACTACCACTGGGCTGTTCAGGGTGCAGAGAGCTTCCTTCAGCAGATCAAATCCAGTTTAATGATCTCCTCCACTGGCTTTAAAAATGACCGAGAGGAGCTCCGCTATATTCAA[C/T]AGATCTTCAGCTCTCTTGCTGAGGGTTTCCAGGCCCGTTTGTCAGAAATTGGTGCTTGCGTGCCCCAGCAAACATGCCTCTCCATCCCTCTCACTGAGCAGCTTCATATAGAGGTTTTGAGTTGCTTTTTAGTACAAGATGCCAAATTAGAAGCTCAGGCTCAATTCCAACTGGAGGCCTTACAGAGGTTAGTCCTACTCTTTAAAGTGCATGGTTTATTATTATTATTTTTTAATTGCAGTGTGGTGACGTTTACTTATGATTCATATTGTCGCATTCACAGTGCTTTGTTGTTGACATTTTCATACTAAATTGGAAAATCATTTCGTAATTGCTTTATGTGGGGGACTTACGTTTTTGGACTAACAGGAAAATATACTTTTAATAAGTGGTCAAGCTTTTTCTGAAAAAGCTCTTTTAGTATCTGTCCTTGGAAACATTTACCTCAGCAAAACTACTCTGATACAATTATTCTAAAAGGTTTTATGCCTGTTTGGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17499
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027454 | Essential Splice Site | 5729 | 8864 | 42 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21793826)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21821993 |
GRCz11 | 20 | 21721666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGCCAAATTAGAAGCTCARGCTCAATTCCAACTGGAGGCCTTACAGAG[G/T]TTAGTCCTACTCTWTAAAGTGCATGGTTTATTATTATTATTTTTTAATTG
Long Flanking Sequence:
TATACAGTTATCTCCCAACGTATGCAGTTGAGAAAATTAGTTGATAATAATATCTGTAGGAGGGAAAGTGCCATACAATGCATTTCTGTTTTGGGGAAAAGCATACATCAATTTTTGTAAAACTCAACATTATTAATGCTTTTTCTGATATTTTGTTTGATCCAGGACAAGCTGCTCCAAGCTCAGGAGGCATTAAAGCACTACCACTGGGCTGTTCAGGGTGCAGAGAGCTTCCTTCAGCAGATCAAATCCAGTTTAATGATCTCCTCCACTGGCTTTAAAAATGACCGAGAGGAGCTCCGCTATATTCAACAGATCTTCAGCTCTCTTGCTGAGGGTTTCCAGGCCCGTTTGTCAGAAATTGGTGCTTGCGTGCCCCAGCAAACATGCCTCTCCATCCCTCTCACTGAGCAGCTTCATATAGAGGTTTTGAGTTGCTTTTTAGTACAAGATGCCAAATTAGAAGCTCAGGCTCAATTCCAACTGGAGGCCTTACAGAG[G/T]TTAGTCCTACTCTTTAAAGTGCATGGTTTATTATTATTATTTTTTAATTGCAGTGTGGTGACGTTTACTTATGATTCATATTGTCGCATTCACAGTGCTTTGTTGTTGACATTTTCATACTAAATTGGAAAATCATTTCGTAATTGCTTTATGTGGGGGACTTACGTTTTTGGACTAACAGGAAAATATACTTTTAATAAGTGGTCAAGCTTTTTCTGAAAAAGCTCTTTTAGTATCTGTCCTTGGAAACATTTACCTCAGCAAAACTACTCTGATACAATTATTCTAAAAGGTTTTATGCCTGTTTGGTTAAATTAAATGTACTTTTCTATTTTTTCTGCTCCAATTTAGGCGCATGAGAGACCAAACCGTACACTTGAGTCATCATGAAGAAATGAGCCAGCTTCTCAAAAATGCTGATTCTCAAATCTCTAAATGCTTCAGTCACAAACCCACTGATCCTGAATCATGCCAAGTACATCAGCTGAAAGTGAAGGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23679
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 6326 | 8864 | 53 | 98 |
ENSDART00000131967 | Nonsense | 345 | 426 | 7 | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21781091)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21809258 |
GRCz11 | 20 | 21708931 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGTCTTCCAGCAGGGGCAGAGCAAACTCTCACAGTCTTCAGTCGCTCT[C/T]AAGAGCTCCTGCAACCCATCCAAGAGCTCCAGCAGCTCAGTGTGCAGCAC
Long Flanking Sequence:
AGTTTTTTTAAGGAACTTCATATGCTCACCAAGGCTGCATTTATTTGATCAAAATTAGTCATACTGTGAACTATTTTCATTAAATATTGCACTTATATTTTTCTATATTTTTACTGTTGTTTTATTTTTTATAACTAACTAACTTTTCCACATTTTTAAATTCACTCATTGCTTCCATGTAGGAGATGGATGCCATTGAAGCAGAGGTGAAGACGATGGAGAAAAATGTAACTAAAATCAGAACAATTCTTTCAGCCTCTGACACACAAAACATCTCTCCCGAGGAGCATCTGGAAAACATACAGGTATAACAAACGATTCGTCTCACCCCCTTCTGTTTCAGCTGATCTAGTTTTACATGTCTCTACTCTCCTCTGTTCCAGGTCATTCTGGATAATGTCCAGTCCATGAAGAGGACCATTGATGAGATCGAGAGCTGCAGGCCAGGTCTGGGTCTTCCAGCAGGGGCAGAGCAAACTCTCACAGTCTTCAGTCGCTCT[C/T]AAGAGCTCCTGCAACCCATCCAAGAGCTCCAGCAGCTCAGTGTGCAGCACAGCGCAGCACTAACGGTCTGTTCACTCTCTCTCTCTCTCTCTCTCTCAAGCCTGGTTCATACTTCTGCGTCAAGTGACTGGCGTAACCAATGGCGCATGCAACGTGCGTGGCTGTGCATTTATACTTCTGCGCGTTATCTCTGTTGGTCTGCATTAACACTTCCGAAACACTAGTTGGCAGTGAGGTGTAAATGTTCCTCTGTGTTGAGTTTCTTCGCTGCTGTTTTGCTTTTCCTGTACACTTCCTGAATGTACAAGTGGCTCAAACTCGCTCATTTTGAGGCAGGAGCCGGCGGACGTGCAACTTTAACTATGAGGTAAACACAGAACAAAACTTTCCATCCGGAGCTCCTTCACGGTTCTCCACACTTTTCCATCGCCTGATGGAGCGATTGTAAACAATCGCTCCATCAGGCTCGCACCATTCGTGCGGCTCTCGGTCCCGCCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9101
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 6352 | 8864 | 54 | 98 |
ENSDART00000131967 | Nonsense | 371 | 426 | 8 | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21779715)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21807882 |
GRCz11 | 20 | 21707555 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTACAAGTTTAAAGACTTAATGAAACTTTTTTTTNNCTAGGCCTCTATTGGA[C/T]ARCCAGCTGAATTGATTCTCCCTTCAGACCAACCCTCAGAAGTGCCGATG
Long Flanking Sequence:
TAAAAATACATATTTTAGAAACCAAAAGGACAGTGAAGCTTGATAAATTGATTTGGCACATGCATTTTCAGCAGTTGCAGCATCAAGTAGAGGCATATAAAATGGCCTTTGGACTAGTTAAAGCCATTTCAAAGAACATGATATTAGTTAGTGCAGTAAATTTGTGGAGTTTTTGGTGACCGTGACCAGAGCATAACCTCTTGTCTTTGCTTTCATGTCTGTGGGAATGAAAGAAGACTAGAAAATCCCTGCGTATAAAGCCAACTCAGAGAAGAGATGTGTGGGAACCTTGAATTCTCTGATTGTGCTTAAAAATGAAGTGCTAAAATGGTGCATCACTAAATCATTGCAGGCTTGACTTTATTGGCAAAGAGTAATATCCTGTAAATACACTCTTGCGGATGTTCTCATGATTTTTTTCATGTGACGCTATGACCTTGACTTTGATTTGTACAAGTTTAAAGACTTAATGAAACTTTTTTTTCTAGGCCTCTATTGGA[C/T]AGCCAGCTGAATTGATTCTCCCTTCAGACCAACCCTCAGAAGTGCCGATGCCACAGCTTTATTCTGAAGATGTGAAGGTGAGTCCATCAGTCCAGTCAAAAACACAGCTCAAAGTTATTCCTTCCCCAGCTCAGAATACACCTTGTAGGCCCTTTTTACACCTGATGCTAATAAGATGCGGTTTGACTGATCAGATAATATGTGGATGAGAGTGAGATACTCTGCTGTTTACACCTGCTATAATTCATCTTGTTTGTCCACTTTCAACCACTTTTCTGCAATGAAGAGGTATACGGGTGTGTTTATGCTCTGGCTTTTTCAGATTTTTTTTTTTTTTCAATTTAATATGGTGTAATGAGCTTTATATACTGTCCAGTTAAAAATTTTACATTATGTAAAGACTTTTTTGAACTTTTGGTTTTTGGTATGATTGGCATTTTGGTAAATTATTTTGATTCCCTTTTGCTCATTTTGTTGACTATTAGTCAAATTGCAAATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37014
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 6687 | 8864 | 58 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21774374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21802541 |
GRCz11 | 20 | 21702214 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACAGCCGTTTACCAGAGCAGCACCCCATCTCAGGAACACACACTTCAT[C/T]AGACAACAGCCGTCAGCAAGTCTGAAGATCAGGAGAGTTTGGTCCAGCTT
Long Flanking Sequence:
GTATAAACTTAGAAACTGAGATGTCTGATACAGAATCAGCCAAGCCAGGTATTGATTCAAAAATCACCAAGTTACAAAGTGAAGAAGATCTTCAAAAGATGTCTGAATCTGGGGATGAGAAAGAAGAACCTATGAATGGTGAAATGAGCACAAGAAATTCAATTAAAACTACAGTTCATAATGAAGGTTTAATTTCAAAGACACTCGACACTGACCCAATAAATGTTACTGATGGCGATCAGACCCAGACAGAGGCAAAACCTCCAGACGCTAATGCTTCTCTTGGCATCACAGAATCTGTTTCACAGGAAGATGCAATGCTGGTAATTCTGTCAAACCCAACTGTAAACTTGCATGTATCATCTGATTTAAAGTACAGCAAATTAAAAATATTTGTCTAACTAAATACTACAATCTTGACTCTCCAGGATTTACAGATAGATGTGAATGAGACAGCCGTTTACCAGAGCAGCACCCCATCTCAGGAACACACACTTCAT[C/T]AGACAACAGCCGTCAGCAAGTCTGAAGATCAGGAGAGTTTGGTCCAGCTTCTCTCCTCATTGAAGGAAACATCACAGGATATCAGTTCTTCTGAGGTCAGTTTCAGTCATGAAAAATGCCTTAAGAAACCAATGTGTCTTGATTATTTTTCTTTGTTTATGGCTGTTGCTTAATATTTAAAAATTGTTCTTGAAATAAGTTATTTGTTTTCAGAAAGGCTGCAGATATTACTTGCAAATATTTCACAGTAGTATAACAGCAATATTGTGAAATTTTATTATAATGTAAAGTAATTGTTGTCTAGTTTAATAAACTGTAAAATGATCACATGGTTTAAATTCAATAAAAGCTGTAATATCATGAATTATCAATACATATATCTCATGTCTATTTTTTATTTTATAATGTATTTTAGTATGTAATTTACTTAATTGCAAATATGAAATGTTGTCATCAATGACAAAAATGTAAATGTAAACATCAATATATTGATGTTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43421
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 6763 | 8864 | 60 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21771847)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21800014 |
GRCz11 | 20 | 21699687 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGTTCTGTAAGAATGTGCAGGGCGGCACCTGGATGTTAGTTATTGAC[C/T]AAAAGAAAACAGCGGGACAAAATACCGAGGAGATTCAGAGATGCTGTGAA
Long Flanking Sequence:
CGGTGTTTGATGTAATCTCAACCGAAACACGAAGAGAAGGTAGGACTTAGTGTAGCCCCTTCCCTTTTTAAAAACAGCCAGTAGCGTTTATCACAGCTCAGCTGGTGAGAGTGGTTGAGCTTAAGTGCATCAAATGAAAAGCAAATAAGAAGCATCATGAAGAGGGTGGGGCATGTCAGATACAAGAGAGCATTTGATTGGTTATGATTTGATAAGAAACTGAAGTATGAGGTGACATGAATAAAACTGTTGACCTATTTGGGCGGAAGTGACAAACTACAAGCTTTACATGTTTGTATCAGTTTTATACTTATAAACGCGATTTATATAACTGTTTTGAAGCACACTAGCTTATAGATACCTTAAACTAATAATACTGTTTAAATTTCATGGGACCATTAAGTTCACAATGCTTTTGTGAAACGCAACCTTGGTGTTACTAATCCAAGTGTTTGTTCTGTAAGAATGTGCAGGGCGGCACCTGGATGTTAGTTATTGAC[C/T]AAAAGAAAACAGCGGGACAAAATACCGAGGAGATTCAGAGATGCTGTGAAGCTCTTTTGAAAGGTCTGCAGGGTCTGCTAGATTTGGGCTCTGATCGGCTCCTGCGCAGTCAGGATGAAGTGCCACACAACTACAGCCAACTGCACAATCTACTTGCTGGACACAAGGTACACTGTAGACTGACCTATTTTAAGTATTGTTTGGAAAAAAAGATGCAGAATGCTAATGATGTTTACTCTTGACTGGGAACAGAAATACTTCCAAGATATGCAGCAGAATCTTGTGATGGTAAAGCTGCTATTCCAAAAGCTGCCAGAAGGGGCAGTGCAGGGCCAAGCAGAAGTTGAGGACCTGATATCGGATCTACTGCATCGAGCACAAAGACAAGGCATCCAAATGCAGCAAAGCTCAGAGGTACAGAGATCGTTTAATTAAAGCAAATATTTTATTTCATAAATTGAGTGTATGACTTTTATTGTTTACAGTAATGTTGTTGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43420
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 6975 | 8864 | 63 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21766312)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21794479 |
GRCz11 | 20 | 21694152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACTGGAAACATCTTCATAATCAGCTACAGCAGAAGATACAGTCTACA[C/T]AGAAAATCAGAATGAATTATGAGAGGTATGGGGAAAATGTAGAATCATTT
Long Flanking Sequence:
AATGCAGTTAAATAAAAAAAGATTTACAAACTACAAAATTTCATGTTTTTTTTTTTACTTTATTAATATTTTATTGAATATTTTTCTTTGGCATATTGATTGGGCCGTACTCATTTTTTCACAGTGATATTAAGTTATTTTATTAAATTGCTTCTAGTTTTAATTTTAATTCTAGGCATTGGTGGTACAATAAAAGTCCCAAGTGAAAGCATGTAAATTGCAGTCTTTAATCTGCCTTTTTATTATTATTATTATTATTATTATTATTATAATTTTTACTATTTTCTTTTCTATTTTGTTTGACTTCATCTCTTTATCAGAAGCTGCACAAGATCCTGGAAGACACATGTTCTCAGGTTTGGGAGACTGAAGACTGCCTCAGGTCTCTACAGAAACAAGGTTACTGTTGTGAACGGAAATTCCAGACTGTCTCAAAATCCCCACTGTTGATGCACTGGAAACATCTTCATAATCAGCTACAGCAGAAGATACAGTCTACA[C/T]AGAAAATCAGAATGAATTATGAGAGGTATGGGGAAAATGTAGAATCATTTTAAAAATCTATAATTTCCCTTCACCAAATTATGATTTTATTTGGAGGTTTGAATTCCTCATGGTTTGGAGCAAATCTTGTTACACTGTAAAGCATACCGAGGTGTGTATTTGTGTGTATAGGTTTCAGCGTGACTCAACAGAACTAGAGGAGTGGATGAGATGTGCTCATGAACAGCTTCAGAAGTGGAAGAGTTTCTCTGGTTCAGATACGCCGGAGTCCAGAATGGCTTTTACCCAGCTCATGGTGACTTGATCTCTCTTTTATATTGTCTGCCCACATTCGCCATGCCCAGTGTTGTGACTTTCATTGTGTGTTCAGGAGTTCTTCAAGGATCTGGAGGTTCGTTCTGCACAGAAAGTGTCAGCAGAATCCACAGGCACACAGATCCTTCAGCTAACAAACAGTGAAGCCCCAGATCTGCGGACACGACTGGCTAACCTCCAGGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37013
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 6981 | 8864 | 63 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21766292)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21794459 |
GRCz11 | 20 | 21694132 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCAGCTACAGCAGAAGATACAGTCTACACAGAAAATCAGAATGAATTA[T/A]GAGAGGTATGGGGAAAATGTAGAATCATTTTAAAAATCTATAATTTCCCT
Long Flanking Sequence:
GATTTACAAACTACAAAATTTCATGTTTTTTTTTTTACTTTATTAATATTTTATTGAATATTTTTCTTTGGCATATTGATTGGGCCGTACTCATTTTTTCACAGTGATATTAAGTTATTTTATTAAATTGCTTCTAGTTTTAATTTTAATTCTAGGCATTGGTGGTACAATAAAAGTCCCAAGTGAAAGCATGTAAATTGCAGTCTTTAATCTGCCTTTTTATTATTATTATTATTATTATTATTATTATAATTTTTACTATTTTCTTTTCTATTTTGTTTGACTTCATCTCTTTATCAGAAGCTGCACAAGATCCTGGAAGACACATGTTCTCAGGTTTGGGAGACTGAAGACTGCCTCAGGTCTCTACAGAAACAAGGTTACTGTTGTGAACGGAAATTCCAGACTGTCTCAAAATCCCCACTGTTGATGCACTGGAAACATCTTCATAATCAGCTACAGCAGAAGATACAGTCTACACAGAAAATCAGAATGAATTA[T/A]GAGAGGTATGGGGAAAATGTAGAATCATTTTAAAAATCTATAATTTCCCTTCACCAAATTATGATTTTATTTGGAGGTTTGAATTCCTCATGGTTTGGAGCAAATCTTGTTACACTGTAAAGCATACCGAGGTGTGTATTTGTGTGTATAGGTTTCAGCGTGACTCAACAGAACTAGAGGAGTGGATGAGATGTGCTCATGAACAGCTTCAGAAGTGGAAGAGTTTCTCTGGTTCAGATACGCCGGAGTCCAGAATGGCTTTTACCCAGCTCATGGTGACTTGATCTCTCTTTTATATTGTCTGCCCACATTCGCCATGCCCAGTGTTGTGACTTTCATTGTGTGTTCAGGAGTTCTTCAAGGATCTGGAGGTTCGTTCTGCACAGAAAGTGTCAGCAGAATCCACAGGCACACAGATCCTTCAGCTAACAAACAGTGAAGCCCCAGATCTGCGGACACGACTGGCTAACCTCCAGGAGGAATGGACAAAACTGACCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37012
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Essential Splice Site | 6983 | 8864 | 63 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21766285)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21794452 |
GRCz11 | 20 | 21694125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAGCAGAAGATACAGTCTACACAGAAAATCAGAATGAATTATGAGAGG[T/C]ATGGGGAAAATGTAGAATCATTTTAAAAATCTATAATTTCCCTTCACCAA
Long Flanking Sequence:
AAACTACAAAATTTCATGTTTTTTTTTTTACTTTATTAATATTTTATTGAATATTTTTCTTTGGCATATTGATTGGGCCGTACTCATTTTTTCACAGTGATATTAAGTTATTTTATTAAATTGCTTCTAGTTTTAATTTTAATTCTAGGCATTGGTGGTACAATAAAAGTCCCAAGTGAAAGCATGTAAATTGCAGTCTTTAATCTGCCTTTTTATTATTATTATTATTATTATTATTATTATAATTTTTACTATTTTCTTTTCTATTTTGTTTGACTTCATCTCTTTATCAGAAGCTGCACAAGATCCTGGAAGACACATGTTCTCAGGTTTGGGAGACTGAAGACTGCCTCAGGTCTCTACAGAAACAAGGTTACTGTTGTGAACGGAAATTCCAGACTGTCTCAAAATCCCCACTGTTGATGCACTGGAAACATCTTCATAATCAGCTACAGCAGAAGATACAGTCTACACAGAAAATCAGAATGAATTATGAGAGG[T/C]ATGGGGAAAATGTAGAATCATTTTAAAAATCTATAATTTCCCTTCACCAAATTATGATTTTATTTGGAGGTTTGAATTCCTCATGGTTTGGAGCAAATCTTGTTACACTGTAAAGCATACCGAGGTGTGTATTTGTGTGTATAGGTTTCAGCGTGACTCAACAGAACTAGAGGAGTGGATGAGATGTGCTCATGAACAGCTTCAGAAGTGGAAGAGTTTCTCTGGTTCAGATACGCCGGAGTCCAGAATGGCTTTTACCCAGCTCATGGTGACTTGATCTCTCTTTTATATTGTCTGCCCACATTCGCCATGCCCAGTGTTGTGACTTTCATTGTGTGTTCAGGAGTTCTTCAAGGATCTGGAGGTTCGTTCTGCACAGAAAGTGTCAGCAGAATCCACAGGCACACAGATCCTTCAGCTAACAAACAGTGAAGCCCCAGATCTGCGGACACGACTGGCTAACCTCCAGGAGGAATGGACAAAACTGACCAGCGTGCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23678
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 7083 | 8864 | 65 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21765767)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21793934 |
GRCz11 | 20 | 21693607 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGGAATGGACAAAACTGACCAGCGTGCTGCCCGCTCTTCAACAGACA[C/T]AGCAAGAAGTATTACTAATGTCTCATCTTCACTCCCTCTGTCACTTCATT
Long Flanking Sequence:
TCATTTTAAAAATCTATAATTTCCCTTCACCAAATTATGATTTTATTTGGAGGTTTGAATTCCTCATGGTTTGGAGCAAATCTTGTTACACTGTAAAGCATACCGAGGTGTGTATTTGTGTGTATAGGTTTCAGCGTGACTCAACAGAACTAGAGGAGTGGATGAGATGTGCTCATGAACAGCTTCAGAAGTGGAAGAGTTTCTCTGGTTCAGATACGCCGGAGTCCAGAATGGCTTTTACCCAGCTCATGGTGACTTGATCTCTCTTTTATATTGTCTGCCCACATTCGCCATGCCCAGTGTTGTGACTTTCATTGTGTGTTCAGGAGTTCTTCAAGGATCTGGAGGTTCGTTCTGCACAGAAAGTGTCAGCAGAATCCACAGGCACACAGATCCTTCAGCTAACAAACAGTGAAGCCCCAGATCTGCGGACACGACTGGCTAACCTCCAGGAGGAATGGACAAAACTGACCAGCGTGCTGCCCGCTCTTCAACAGACA[C/T]AGCAAGAAGTATTACTAATGTCTCATCTTCACTCCCTCTGTCACTTCATTTGCTCTTAATAGCTTCATCAAACAGATATTGCTACAGTAAGCGTCTCTTTATCTTCTTAGCTGTTGGAAGGCCAGTCAGACAGTCAGATCTTGGCTGATTTGTCTTCCTGGCTGCAGCATATAGAGAGGCGGCTGGAGGATGAAAGCTCGGGGGTTCATTGTGCCCTGGATTCATCAGAGCTGTCTAGACATTTACAAGCTTTAAAGGTATTGCACCTACGCTTTTAATTCTTTTGATTTGTATAATTTGTGAATATTACAGTCATCTTGTTAGGTTCGTCTGAAGTTTCTTATGCTCTGCTTTAAAAATGCTTGTTCTGCTGCAAAATCTGAATTCTGTTTACTAAATATATATTTGGACTGACTTAATATTAGTTGACCTTAACTAATATGTACTTGCACTGAAATTAGACAGTTAATGGACTTCCTCTGTAAATACATGTTTTTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13943
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Essential Splice Site | 7086 | 8864 | 66 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21765658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21793825 |
GRCz11 | 20 | 21693498 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAGCTTCATCAAACAGATATTGCTAYAGTAAGCGTCTCTTTATCTTCTT[A/G]GCTGTTGGAAGGCCAGTCAGACAGTCAGATCTTGRCTGATTTGTCTTCCT
Long Flanking Sequence:
GTGTATTTGTGTGTATAGGTTTCAGCGTGACTCAACAGAACTAGAGGAGTGGATGAGATGTGCTCATGAACAGCTTCAGAAGTGGAAGAGTTTCTCTGGTTCAGATACGCCGGAGTCCAGAATGGCTTTTACCCAGCTCATGGTGACTTGATCTCTCTTTTATATTGTCTGCCCACATTCGCCATGCCCAGTGTTGTGACTTTCATTGTGTGTTCAGGAGTTCTTCAAGGATCTGGAGGTTCGTTCTGCACAGAAAGTGTCAGCAGAATCCACAGGCACACAGATCCTTCAGCTAACAAACAGTGAAGCCCCAGATCTGCGGACACGACTGGCTAACCTCCAGGAGGAATGGACAAAACTGACCAGCGTGCTGCCCGCTCTTCAACAGACACAGCAAGAAGTATTACTAATGTCTCATCTTCACTCCCTCTGTCACTTCATTTGCTCTTAATAGCTTCATCAAACAGATATTGCTACAGTAAGCGTCTCTTTATCTTCTT[A/G]GCTGTTGGAAGGCCAGTCAGACAGTCAGATCTTGGCTGATTTGTCTTCCTGGCTGCAGCATATAGAGAGGCGGCTGGAGGATGAAAGCTCGGGGGTTCATTGTGCCCTGGATTCATCAGAGCTGTCTAGACATTTACAAGCTTTAAAGGTATTGCACCTACGCTTTTAATTCTTTTGATTTGTATAATTTGTGAATATTACAGTCATCTTGTTAGGTTCGTCTGAAGTTTCTTATGCTCTGCTTTAAAAATGCTTGTTCTGCTGCAAAATCTGAATTCTGTTTACTAAATATATATTTGGACTGACTTAATATTAGTTGACCTTAACTAATATGTACTTGCACTGAAATTAGACAGTTAATGGACTTCCTCTGTAAATACATGTTTTTACATTGTGCTTATTGTTGAATAAATACCTGTAATTACATTTTTAATTACATTGTTGAAACTTTAACCCACACTTCACAATTCACAATATTATAATTTACAAGTTTATATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23677
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 7208 | 8864 | 68 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21763345)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21791512 |
GRCz11 | 20 | 21691185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTGTCTCCAGATACATGATGTGGAGGACCAATGGCAAGCCTGTGGAGAC[A/T]GAGAAAAGCTATTGCGCTGTATACACAGCTGGATTTCTCAGCATATGGAA
Long Flanking Sequence:
ACTCAAATTTGACAAAAATGTCAGATAAAACCTTTAAATTCTAAGGTTGACGAAATGTTTGCTGAGGATCTGTTTACTGATAATGTTTAACTTTAGTTAGTAAGTTCAGTTAATGCACATTATGTTCCACTTGTATTTTGCTGTGTTTGTTATATGTAATGGATCTAATGAAATAACGACTAGTCAGTGTGCATCTCCGATCATCTAGTCCTTTTTTATGTTGTGTTTTTTACTCACAGTTTTAGATTTTGCATTGAGTAATCTACTTAAATTGTGGAAGATTACAAATTTTAATTGTGTTTTCAAGAACATTTAATTTACAGGTTTTCATAAACAATTTTAAAGGTTTTTTTTTTCTTTCTTGCTGTCTGTAAGTTAGCAATCAAAAATGCATGATTATTACATAGATTTAAATTCTAACATATAGCCTCTTACAATGTGATGGTTTCTGTTGTCTCCAGATACATGATGTGGAGGACCAATGGCAAGCCTGTGGAGAC[A/T]GAGAAAAGCTATTGCGCTGTATACACAGCTGGATTTCTCAGCATATGGAATGGGTGAAGAACAGCTGGAGACCAGGGAGCTGCTCACAGATTGAGCAAACATTACAAGAGTGCGAGGTGAGTTCAACCAACCTGAAGATTTTTTTTTTGTCACGATTTTGATAGGTGTGAGAGTGAAATCGAATCAAAGGAGAGCTTTTAAAGTGAGAAACATCAGAAAAGTCACACAGTGCTTTGTTTCAGGGCACAGAGAAGCGGCTGCAGGTGAAGTCCATTGAGCTGAAGGGCTTGGAAGCTCTTCATCTGTTCAAACAGCAGGACAGAGAACATCCTGGAGATCAAGCATTCTCCAGGCAGCTCAATTCAGCCATAGAGGACTGCCAAACTTTGAGCCAACAGGTAAGTTCCTTGAAACTTGTTTTACTGTGTTTTTTTTATTAAATATTTTATTTAACAGGGATGTACTGTATTGTATTGAACAAAGCTGATGGTAAAGACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23676
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 7465 | 8864 | 72 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21758941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21787108 |
GRCz11 | 20 | 21686781 |
KASP Assay ID:
2261-4192.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGATAGAGAAGAAAACACTGTAGAAATGCTCATCAGCAGGATGCAGTA[C/A]ATTAGTGTGAGTACAAACATATTACAGGTGCAAACGTTTTTATGGTATGA
Long Flanking Sequence:
AGAAAAAATCAAGCCCTTTGCATTTAAACTTCTGTCTGATCGCCTTGAGAAGGAGAGAATCCGGTGAGTATTTTTAACCTCTCAGTACTATACTTGACACTTACCTAAAATTGCAGTGTCACCAAATTGTTAATATCAGTATATCTCTGTCTGAAATTGAGTCAGCATCAGTGAGGAAGCAATAGCTGGTAGCGTTTCTTTATAAATTGTCAGATGAATGTTTATTGGATTGATTGATTAGTTCAGCTAATGTTTGCATGTTTACTGAACCTGTGTGGCTGTTCATGTTTATTTGTTTTCAGACGTCATACAGTAACTGAAGACGTTTGTGAAGATTTGCTAAAAGCCCAGAATGCATTGCAGCTCTGGCTGGGATATGAGCATCTCACAGAAGAGTGTCGTGTTCTTTTGAATCAGCATTGGGAGAGACTTGGAGAGCTTATGAATTCATCAGATAGAGAAGAAAACACTGTAGAAATGCTCATCAGCAGGATGCAGTA[C/A]ATTAGTGTGAGTACAAACATATTACAGGTGCAAACGTTTTTATGGTATGATGTGGTCCAAATGTATTGAAATGTATTTTAATATTCTGGCGAAGTCGTGGGACCAAGAATAGTTCGTCCAATCAAAATGCTGGGTCTGAGCATTACAATAGGCTATCCTGCCTGCCTTTCAAAATATGTTATTGCATATCTCCGCTCAACTTGAAAATGGAGAAAGCATTACATCATTGGAGCGTTCACATGTGCGCTTCAGACAGAGAACAGCAGACAAAGTTTGGTGTTGTAAATACTAACTGTACTATAAAGTTGTCTCTCCGGTGAATGTTGAGTGATGTATTTTAGTTATGTTGTCTTGTGCATATTTACGTATTCAGAAGGCGTGGCTTTGAATGGTAATTTGCAAGGTGGGATGTAGGCTTTCATTGCTATCAGGCTGACATTTGAAATTTCCAAGATCTCCTATTGGAGGTCATAATGAAAGTCTATGCTATAATATCATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37011
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 7633 | 8864 | 76 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | None | None | 1000 | None | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21755088)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21783255 |
GRCz11 | 20 | 21682928 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTAGGAAGATGTATGGAGAGCTGCTGCGTGATCAGAACTTCCAGCAG[A/T]AGTGCCAGTGCTGGATGGAGCTCCTGGACAAAATGGAGACTGATTTAGCC
Long Flanking Sequence:
CTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTTTACCTTTCCACCTATCCACCCATCCATCTCTCTATCTATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCACCTCCCTTCTAAAATATCATATTATAATAACAATACATATTATAAAAATACAAATATATCATGACATGTTTTCCCTAGAAAACAGACTTCACTGTAACATTACCTGTATCTAATGCCAAAGCACATCACTGTCTGTAGGAAGATGTATGGAGAGCTGCTGCGTGATCAGAACTTCCAGCAG[A/T]AGTGCCAGTGCTGGATGGAGCTCCTGGACAAAATGGAGACTGATTTAGCCAATCCGACACCTGGAAACTGTTCTTCTGTAAGAGATCTTCTTGCTGCACATCAGGTAGAGCTTATTCTTTAAATTTAAGCTCTTTTGATATTTAGAAATTGCAGGCTTATAATACTAATTGTGTTGTTTCACAATGACCATATAAGCATGATAAATAATAAAAAATATGTTAAAGAAGGTTTATGCTCACCAAAGCTATTTTAATTTTTGTTTAGTATCATAAAATGTTAATACAATTTTAAAAAATACTTAATATTTTATATAAAAATATGACTCTGTTATTTTTATTTAATATTATTTTAGTCTCTCAGTCTCTCGTACAATCCTTTTAAAAATCATTATAGTATGCTGATTTGGTAATCAAACATTGATTATCAGTAATATTGCTGCTTATTACTATTGAAAAGTCTTAAAGTTAATATGTTTCAGAGTGCATAGATTAATCTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11511
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 8058 | 8864 | 84 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | Nonsense | 194 | 1000 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21732607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21760774 |
GRCz11 | 20 | 21660447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTCTRTTTCAGGGKGAAGAAGCTGACCGAGACTTTGGTGACAGTACAR[C/T]AGTTGGATAAGAACATGAATAACCTTCGCTCTTGGCTYACGCGCATTGAG
Long Flanking Sequence:
GAGGGGCACAATGGGGTCAGAGGGACAGGCTGTACTCAGGCACGCTATAATCACAGCCGACCATCTGCAGGTATGGCCAAACAGCGTAACCAGAAGCTGCCCACTGTCACACTTAAATGGTTCAATCTAATCTCACACAAACACCCTTTGTCTGTTTCAGTGTCATCTGACCTGGAGTTATCAGACCTTTTTATTTTTATTTTTTGATGATGTTTTGTAACTTTGACAGAATTTTATTGGGTTCCTGCCAAACTGCACAGTCCCAGATCCCAAATAAAACAATTGCTTGACTGATTTATTAAAAGGGTTAGTGCGTTTTAGTATGGAGAAAACTGCTTGGCATTCATAGACAATCATTTTTTATCTAGTGGAAATATTTTTTTAGGTCTTTTGGACGCATTCGGGTATAATTTATGGTGTTCAATTTTTCAAAGCGAATATGCTGTATCTCTGTCTGTTTCAGGGGGAAGAAGCTGACCGAGACTTTGGTGACAGTACAA[C/T]AGTTGGATAAGAACATGAATAACCTTCGCTCTTGGCTCACGCGCATTGAGGCTGAGCTATCCAAACCAGTTCACTACAGTATCTGCCATAGAGAAGAGATTCAGAAGAGACTGGCAGAGCAACAGGTTGGTAAATTGCAGTGATGTAATCTATTCTAGTATGGACAAATATTAAATGCAAGAGGGGATTTTGTTCTTTGTAGATTAAGAAAAAAAAAATGACATCTTTTTAAAAGCTATAGAAAAATCAACAAACTTAACTAAAATAAAGACATGTTTTGATTAGATTTTGGCATACTTTTTGTACAAAATAACCATGCAAGATGGTAACTCTGATTTTAAATAAATTTTTATTTATTTTATTTTATTTATTTATTTGTATTTTAATATTTATTTAATTATTTTGTTTGTTTATTTATTTTTTAATTTTTTTATTTTTGGGACAATCTGCCAGAAATGTATATTATCTGTGCCTGAAATAAAAACATAAATACAGTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43419
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Essential Splice Site | 8385 | 8864 | 90 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | Essential Splice Site | 521 | 1000 | 10 | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21725326)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21753493 |
GRCz11 | 20 | 21653166 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGATTCAGATAATATGAGTATGAGTAACAATGTTTTTCTTCTGTAACA[G/T]TTGCAGGAGCATCCAGACGTGTATGATGGCGAGCGGTCGAGAGAGACACA
Long Flanking Sequence:
GTTTGGACATCCCCGCTCTAAGGGGCTTCTAAAATGAGTCTATTTCAAAAAAGGTTTTGTTTTTTTTAAATAGAAAAAAAAAGAAAGAGAATAGATGACGGCTTGTATTTAGCAGGAATGCCTTTAATTAAAGTGATTGTAAAGACAAGAATTAGGTTCTAGAAAATTTAGCCAATCTTTTGAACTTATTCCTGTTAATCACAAATCTTTTAATTAAGAAAACTAAAACACAAAGTTGGTAAGAGGCATAAATGTTTCTTCAACAGCAATTCAGCATGTTTCTAAAGGATCATGTATTTCAAAATTTGTTCATACAGAAAAATGATTTCTATATATTGCAATATTTTGCAATATTCTAGTTTTTAGAATATTAAAATGTGTTTTTTTATCAAATTAATAATCTTACGCAAATTCTCTTTGCAGTGACAAAGATGACCAAATAATTTTGCATATGATTCAGATAATATGAGTATGAGTAACAATGTTTTTCTTCTGTAACA[G/T]TTGCAGGAGCATCCAGACGTGTATGATGGCGAGCGGTCGAGAGAGACACAGAGTCCTCCTTCCTCTAGTCAGCCCTCCATGTGCTTGTTATCTCCACCTCAGGAGCGTTCAGGACGTGAAACCCCCGTCAGTGTAGACTCCATTCCTCTGGAGTGGGACCACACTGGGGATGTCGGCGGCTCTTCATCACATGATGAGGAGGAGGAGGATGCTGCCTTCTTCTCAGCCCTGTCAGGTAAATACACTTTTGCTGGTGTCATCTTAAGCTCCCTTCACATTTCATCTCATTTTTTATCTCAGGTTGTTACTTCTCGGGACATCTGTTATTCCATGCTGTAATTTTCCCCATTAGATGAAAGCAAAAGCATACACTTTTTGTGTTTGCCTCCTTAAATGCAAATGAGCTGCTGTTCCGCACCCACATTTTCTGAATAGGGTGTTTCTCCAATGGAGACTCTTAAAAGCACATTTAACACAAAAAAACAGAACCTTTTATTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5949
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 8395 | 8864 | 90 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | Nonsense | 531 | 1000 | 10 | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21725295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21753462 |
GRCz11 | 20 | 21653135 |
KASP Assay ID:
554-3913.1 (used for ordering genotyping assays)
KASP Sequence:
ATGTTTTTCTTCTGTAACAGTTGCAGGAGCATCCAGACGTGTATGATGGC[G/T]AGCGGTCGAGAGAGACACAGAGTCCTCCTTCCTCTAGTCAGCCCTCCATG
Long Flanking Sequence:
AAATGAGTCTATTTCAAAAAAGGTTTTGTTTTTTTTAAATAGAAAAAAAAAGAAAGAGAATAGATGACGGCTTGTATTTAGCAGGAATGCCTTTAATTAAAGTGATTGTAAAGACAAGAATTAGGTTCTAGAAAATTTAGCCAATCTTTTGAACTTATTCCTGTTAATCACAAATCTTTTAATTAAGAAAACTAAAACACAAAGTTGGTAAGAGGCATAAATGTTTCTTCAACAGCAATTCAGCATGTTTCTAAAGGATCATGTATTTCAAAATTTGTTCATACAGAAAAATGATTTCTATATATTGCAATATTTTGCAATATTCTAGTTTTTAGAATATTAAAATGTGTTTTTTTATCAAATTAATAATCTTACGCAAATTCTCTTTGCAGTGACAAAGATGACCAAATAATTTTGCATATGATTCAGATAATATGAGTATGAGTAACAATGTTTTTCTTCTGTAACAGTTGCAGGAGCATCCAGACGTGTATGATGGC[G/T]AGCGGTCGAGAGAGACACAGAGTCCTCCTTCCTCTAGTCAGCCCTCCATGTGCTTGTTATCTCCACCTCAGGAGCGTTCAGGACGTGAAACCCCCGTCAGTGTAGACTCCATTCCTCTGGAGTGGGACCACACTGGGGATGTCGGCGGCTCTTCATCACATGATGAGGAGGAGGAGGATGCTGCCTTCTTCTCAGCCCTGTCAGGTAAATACACTTTTGCTGGTGTCATCTTAAGCTCCCTTCACATTTCATCTCATTTTTTATCTCAGGTTGTTACTTCTCGGGACATCTGTTATTCCATGCTGTAATTTTCCCCATTAGATGAAAGCAAAAGCATACACTTTTTGTGTTTGCCTCCTTAAATGCAAATGAGCTGCTGTTCCGCACCCACATTTTCTGAATAGGGTGTTTCTCCAATGGAGACTCTTAAAAGCACATTTAACACAAAAAAACAGAACCTTTTATTTGTTGTCTTTTCAGTTTCCACTCCTCATATAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15833
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 |
---|---|---|---|---|---|
ENSDART00000027454 | Nonsense | 8497 | 8864 | 92 | 98 |
ENSDART00000131967 | None | None | 426 | None | 10 |
ENSDART00000133286 | Nonsense | 633 | 1000 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 20 (position 21720946)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 21749113 |
GRCz11 | 20 | 21648786 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGMACTTGAGTGAAAGGTGATTGTGATGTGACNNNNGTNNACTGTATGTGAAGGTC[C/T]AGCTGATGTCTGAATGCAGCGGCAKCATCAAGAGTGTGAAGAGGRTTTCT
Long Flanking Sequence:
ACACATATATTGCATGAAATAGTACATCATGAAAATTTACTTGAAAGTCTTGGAAAAATCATGGAAAAGTCATGGAATTTTGGTGGTATGTGTATGAACCATGAAATACAATTATTTGACAACCATGATAAAGCTTAGAAGTTTTGCAGATTCTTAGGTCTAATTTACTACTTTAAAAATGGATGCTGCATAAGGCCAAATTACACTTCACCATCTAAATGAACTTACCTAATTGACCTAAAACTCTCTCTCTCACACACACAGGACAGAATTGGCACTTCCAAAACATGCCTGAAAGGAAATCCTTCCAGCTGGAGTCATCCTCACCTACACACACCAGCACTCCCTTTAAACAAGGCTATGTGAGTATATACCCATTCTTTCTTAACCTAGCGCACCCACAAATCACACACAGTCTTTCTTGTGGAATCAGAAAAGGTAAACACATGTAGCACTTGAGTGAAAGGTGATTGTGATGTGACGTACTGTATGTGAAGGTC[C/T]AGCTGATGTCTGAATGCAGCGGCAGCATCAAGAGTGTGAAGAGGGTTTCTATGATCCTGGATGATGAAGAACAGCAGGAGGAACAAGGACTCACTGGCCTCAACACTGCAGACAAACAGTCAGGTACAGACGCTGACGTCGACAATGACGTCTTGTTTTGAGTGACTCATCTAATCACGTGTACAGGGGACTAGGTCTAGTAAAGCATAAATACTTTTTATCAGCAGAACTACAGCATCAAAACAAAAAAGAACTACAGCATCAGGCTGCTTCATGGTTTTATTGCTAGCTGCATGAGTGGATAGGTAATTAGCTGGATATGTGAGTTGATTGGAGATGAGTGGAGGATGGATGAATGAATGGATTGGTAGTTTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTTAATTCAATGTAGTGGATAGACAAATGTGATTGTGAGAGATGCTTATAGATGAATGGTTGGATCAA
Associated Phenotype:
Not determined