ZMP
birc6
Ensembl ID:
ZFIN ID:
Human Orthologue:
BIRC6
Human Description:
baculoviral IAP repeat-containing 6 [Source:HGNC Symbol;Acc:13516]
Mouse Orthologue:
Birc6
Mouse Description:
baculoviral IAP repeat-containing 6 Gene [Source:MGI Symbol;Acc:MGI:1276108]
Alleles
There are 29 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23063 | Essential Splice Site | Available for shipment | Available now |
sa6471 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23064 | Splice Site, Nonsense | Available for shipment | Available now |
sa42920 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23065 | Nonsense | Available for shipment | Available now |
sa45603 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44872 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10215 | Essential Splice Site | Available for shipment | Available now |
sa17388 | Essential Splice Site | Available for shipment | Available now |
sa23066 | Nonsense | Available for shipment | Available now |
sa36396 | Nonsense | Available for shipment | Available now |
sa23067 | Nonsense | Available for shipment | Available now |
sa36397 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2916 | Nonsense | F2 line generated | Not yet available |
sa13557 | Nonsense | Available for shipment | Available now |
sa13763 | Nonsense | Available for shipment | Available now |
sa39160 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45604 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8438 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17275 | Nonsense | Available for shipment | Available now |
sa36398 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12006 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23063
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Essential Splice Site | 142 | 4870 | 2 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22425705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22575854 |
GRCz11 | 17 | 22595690 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTGTCCAAGCCAGAAGACATGGTCCAGCTGGAGCTGCCCGTCACTGAA[G/A]TAAGATACGTGGCATATTGTGCATATTGATTTATTGTGTATAGCATTGCG
Long Flanking Sequence:
CTGTTAAACATCATTTGGGAAATAAAAAAAAATTATTCACAGGAGGGTGATTAATTTTGATTTGAACTTTATATTGTTTTGAATAATCGGGATTACAGTTATGGCCAAAATAATCGTGATTATGATTTTTCCAATAATCGAGCAGCCCTAATGTGTATCCATTTTTCCTTGAAATAGTTATGAGTTGCTGATGTGGCAATAAAAATAAACAAATAAGTTTGATCTGTATGTTTGTTGAACTAATGTAGAAAAGCTTCAGCCTTATGCATTAATGATCACTCAGCCTCTCTCCTTGTGTGTGTGTGTGTTTTGTGACAGCTAAACCTGGAGGCCGGGTGAGGTGTCAGTACTTCCCAGCTGTGGATAAGGTGCTGTTTGTGGACGATTATGCTGTTGGCTGCAGGAAGGACTTGAATGGGATCCTTCTTTTGGACACGGCTCTCCAGGCCCCCGTGTCCAAGCCAGAAGACATGGTCCAGCTGGAGCTGCCCGTCACTGAA[G/A]TAAGATACGTGGCATATTGTGCATATTGATTTATTGTGTATAGCATTGCGATTGCGAGTTGGCTATGCTTTACCTGACCACTAACAGTAAATGGTTGTAGGTTGACCATCTCAGTACAAAGGTGAGCAATGGTGCATTTTAAGCAGCTTGGAATTATTTTCTTGGGTGCTCTTTTGTTTGATAGGATGATAAATATTTATTTCTGTGAAATCCAAGTATGCATTTTTATAATGTTAAATAGGACTAAATGTGTAATTTGAGTCCAGCACTCCAGATGGTCAGTCTGACTTACAGCTGATAAATGTTTTCAGGGCTTTCATGTCACAGCTGGACTGCACATTGTATTTATTGGTAGGGGTGGGAATCGATATTACAGTGGTTCATCGCTATCACTTTTTGTGGCCTCGCAGTTTTACACATTTTTTTTCATACAATTTGACTTTTTTTAATATTTTAATCTTGACTGGCTGTAGACCACTTTCGATCAATCTCCTCCATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6471
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 491 | 4870 | 10 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22448495)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22598644 |
GRCz11 | 17 | 22618480 |
KASP Assay ID:
554-5426.1 (used for ordering genotyping assays)
KASP Sequence:
AGGAGACGATGGAGGTGAGTTTGGGAGTCACAGCTCTCAGTGTTCTACAA[C/T]AGCCTGAGAAATTGCAGTGGGAGGTGGTGGCYAGTGTTCTTGAGGACACA
Long Flanking Sequence:
TTTGAGGTGAACCCGTATGACCCAGCCATCCTTAGGCAGTTGATCCTGTCTGGGAGCGAACAGCAAAATCTCACAGGCACCGAATTACGCAGACCCACACTCTCATGGCTAGAGGAGGCCACATGCTGCTCTGACTTACCCAAACTAGAGGGGGACAGGTTCTAATCCCACATATTCATAATTTTAGTAAGTCATCTTAAGACTATTGTTGTCTTGATTGATTTTTTTTTGTGTGTGTGTATGTGTGTTTTTGTACATAGTGATGACCAGATAGAGGACTCAGACAGTGAAGAGCATTCCAGATCAGAGTCAGTTACAGGTAAAACATTTATTTTCATGTATTAACAATGTTTATTTATTATTTAGCTGCTATGTTTTGTTTTTTTTGTTTTATTAACATCCTACTAATAGATCTCTCCCCTTCTGTATGTGCAGGCCCATTGGGTCAGAAGGAGACGATGGAGGTGAGTTTGGGAGTCACAGCTCTCAGTGTTCTACAA[C/T]AGCCTGAGAAATTGCAGTGGGAGGTGGTGGCTAGTGTTCTTGAGGACACAGTTAAAGACCTGGAGGAGCTGGGGGCCAATCCTCCACATTCACTGGGCCCCCCTAAAGCAGATAAAGCTAAGGATCGGCCAGCTGAACATCACAACATTCCCTTTCCCTGCCTGCTGGCTGGTGGACTGCTAAGCTATCGGTCAGCGGCTAGTTCTCCACTAGGTCCTCCTCCATCTCGCCGCTCCATGGATAGCCCAGTAAGGACTGCTGCCCCTGAGGGGCTTGCGCCAGACCAGGGGCCTATGGAGATTGAGTCCTGTAACCCTTCAACAGACCTGGGCTCCCCAAACTTACCACCAGCCGCCCCTGTGCATAGGACTATGCCTGTACTGCTCCTGTACAGTATCAAGGAAGCAGATGAGAAGTCTTCAGGGAAGGTGTTCACCCAGATGAACAACCTGATGAGCAAAGGGCTTCATGACGAGGGCTTTACCGTCCCACAGATTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23064
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114100 | Splice Site, Nonsense | 1358 | 4870 | 20 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22456184)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22606333 |
GRCz11 | 17 | 22626169 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCATTGCTCTTTTTCTAAGAGATGTTATGATCTGTTGTCTTTTAGTT[T/A]GAGAGAGGGGAAAGAGGGGCTTTTGACCAAAACCAGAAGACGTCTGACGG
Long Flanking Sequence:
ATGTAAAGTGTGGTATGTAAACAAACATATGAGTGTTTCTAACAAAATGTCTGGTACATCAGTCTCTATTAGTTTGCTACGAGCGAATGATGTGCACAAAGAACGCCCTGTCCCCTTACCGATATTTACTTACAGTAGAAATACATCAACATATCGAAACAAAAGTCTCAGCAACTTCATCTTCATGCAGACTTTTGTTTAAATCTTTCATTGTCTAAATGTGCTTTCTGTCTCTGCTTGTATTTCCCAGAGTGCAACGCTGTGCAATGCTTCAGTTTCCTGAGCTCCACGAAAAGCTGCTAAGAGGTTTGTGTAAGCGTGGAGAAGACAGCCAGAGCTCTGAACACTGTCAGAGTCTCATATTGGACATCCTCTGCTGGCTGGCTGGAGTTTACTCCAATGGACCGTGCAGGTGGGTCTCTGACTCTGTGTTTTAAGTCTCAGGCTTTTATTTCATTGCTCTTTTTCTAAGAGATGTTATGATCTGTTGTCTTTTAGTT[T/A]GAGAGAGGGGAAAGAGGGGCTTTTGACCAAAACCAGAAGACGTCTGACGGACATTATCAGGGCATGCTTCTTTGAGGCCGGGCGCAGTATAGCTCACAAATGCTCTCGCTTTCTTGCACTTTGTATTAGGTGAGTTTGAATTCTGTGTCTTTTTTTCTGTTCTTCAATTTTGGTGGAGAACTATTATACTAGTAAATATGTTATGGTCATTACGTTTAATGGATGAATGTCTTCTGTTTCAGTACTGGTAAAGGAGACCCTGGTCAGCAGGGTTTTGGCCAGGCACTGTTTAAAGCGCTTTTGGATAATATGCCTTATTTGCCTGCTGCTGCCACAGGAGGTGATTTTTAATTTTCCTATTTTAATTTATTTTGTTACTCTTTACTTTTTTTAACACAACTATTCAAATCATGTCTATGTCTTTAAGGAATTTGGAAATTCAGTGATTTAGTAAAATTTCTTATGTTCACCATTCAATAAATAAATAAAAACCACAGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42920
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Essential Splice Site | 1635 | 4870 | 25 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22457858)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22608007 |
GRCz11 | 17 | 22627843 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAAGTTCTCCAGGAGAAGCAGCAACAGCTTCTAAAACTCCAGCAACAG[G/A]TCACATTCTTGCTTAATTGTAATGTTGATTTGTTTTCCATCTAGTTGTGA
Long Flanking Sequence:
CTGGCCTGCTGGAAGTTGAACCTCTGCACTTTACTTGCGTCTCCACTAGTGACGGCACTAGAGTGGAGAGGGATGATGCAAGTATGTTCACCGGTACATATCCCATTTTTCTCTTTCTCTTATCTTGTTTATATTACAACCAACCATGTCATCATGGACCGCACGTTTAAGGTATGGTCAAATTAGCTGAGTTGTTTTCTTTGTACTACAAAACCAAACCACAATTCAGCAAATTTGATTCTTTTCTAAGAAGAACCACATCTTTAGTGATAAAATAGTTTCTATACCCCTGTACTATATATTTTGTTTTAGTGAGCACATTTGGAGTGACGCCTACAGTGACAGGGCTGTCTGCTGGGTCTGTTGGCGAAGCCTCCACTGCTCTGAGCTCGGCTGCACAGGTGGCCCTGCAGTCTCTGTCTCACGCCATGGTGTCCGCCGAACAGCAGCTTCAAGTTCTCCAGGAGAAGCAGCAACAGCTTCTAAAACTCCAGCAACAG[G/A]TCACATTCTTGCTTAATTGTAATGTTGATTTGTTTTCCATCTAGTTGTGAGTTTATTTAATTGGTTGTATTATGAAACAGAAGGCCAAGCTGGAGGCCAAACTTCACCAGACCACCTCAGCAGCAGCCACCGCAGCATCAGGCGTTGTCAACTCTGTGCCATCCAACCCGTCCTCAGCCCCAGGCTTTTTTATCCACCCGTCAGACGTCATCCCACCCACCCCTAAAACCACCCCGCTGTTCATGACACCACCTCTCACCCCGCCCAATGAAGCAGTGTCGGCGGCCATTAGTGTGGAACTGGCTCAGCTTTTCCCAGGATCTGTCATTGATCCTCCACCTGTAAACCTTTCAGCACAGAATAAAAACAACCAGAAAGCGAAACCCGTAAGTCCTGAAAAACCACCAGAAAAAATTCCATTATTTATTTGAGTCTTTTTCTAAAAAAATGATTTTTTTTAAGATGTCGGAAGCTATTTTATTTTTGTGTCAAAGTTGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23065
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 1866 | 4870 | 29 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22460646)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22610795 |
GRCz11 | 17 | 22630631 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGATATGGCAGCACTAATGCCCGGGCTAAAATCCCATTGGGTTTTTATTA[T/A]GGCCACACCTACATCCTGCCATGGGAAAGTGAATTGAAGCTGATGCATGA
Long Flanking Sequence:
GGTACCTAATATCAGGTCTTGTTGTCAATTAGCAGTCTGAAGTCAACTGAAGGGCTTCAGAAATTACAAAAATGGCTTCTAATCAATTTACTGTAGATTAAACAAATGTTTTTCACCTGTAGGTGCAAGGCGGTTTGTGACTCTAGATTTTGGCCGGCCGGTGTTGCTCACGGATGCACTGATCCCCACATGTGCAGACTTGGCCTCACTTTCCATTGACATTTGGACTCTTGGGGAGGAAGTGGATGGGAGGAGACTGGTAGTCGCCACAGATATCAGCACACATTCTCTGATTCTGCATGATTTGCTACCCCCTCCTGTCTGCAGATTCATGAAGGTTTATAAATGCTTATTTTAAAAGAGTGTGAACAGGATTCATAGTGGTCTTTTTAAGAAGCAAGTCACTGTCACTAACTCTCTGTGCCCCTCTCCTAGATCACTGTGATTGGTCGATATGGCAGCACTAATGCCCGGGCTAAAATCCCATTGGGTTTTTATTA[T/A]GGCCACACCTACATCCTGCCATGGGAAAGTGAATTGAAGCTGATGCATGATCCTCTGAGGGGAGAAAGCGAAGCTGCCGGTCAACCGGATCTGGATCAACATTTATCAATGATGGTGGCACTGCAGGAAGACATTCAATGCAGGTCAGTGAAACAGCAAATAAGCATAATTAAATGAGCTCCTGCTGCAGAATACAATCATTTCCAGTTTTTTTTCTTCTCCTTTTTTAAAAAAAAATCTGTATTTTTATTCAAGAATATAATACATTTGTCAAAAATGATAGTAAAGAGAGTGTTAATGAAGCAGTTTTACTTTCACATATAAATGTTCTCATCAAATTCAACAATTTTTTTTAATCAATTTGATTATTATTTTCATATGTAATTTACAGAATCACATAAATGCACAAGTAAACAATATTTTTAGCCACTCTTGCACACTCCCCAACCCTTTCTGCACAGACCTCTTAAATGGACCTTAATGCAACATGAAAAATAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45603
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 1991 | 4870 | 30 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22462189)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22612338 |
GRCz11 | 17 | 22632174 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCACCACGCTGTCCAGAGGCTGCGCGTGTCTCTAGGAGCAACTCGAAAA[C/T]AACTGCCTGAAAATTACGACCCCCGAGAGCTGGTTCAGAACTCTTCTACC
Long Flanking Sequence:
TTGCATAAGCAGTACTCCTATGCAAAGGGGCTTTATAAGACGAGACCCAAATGTAACGTTGATGCTCCTCCATCAAGCACATTTATATGGAAAAGCAGCTCATTGGAATAGAAAAACATGCTCTGTGTGCATGCTTCAAATCCAGCCTTTTAAAATCATTAAAATCTTACCAACATGAAAGTTTTTTTTTTTTTTTTTTTGCTTTGTCCTGGAATTTATTTAGCCCATTTAAGCAGAATTGATTCTAATCTAAGTGCTGATCTTTGTGTAGGTATAATTTGGCCTGTCATCGCCTGGAGACGTTACTTCAGAACATCGACCTGCCACCTCTTAACAGTGCTAATAATGCACAGTATTTCTTGCGTAAGCCTGATAAAGCTGTTGAGGAGGACTCCCGCGTCTTCTCCGCTTACCAAGACTGCATTCAGCTCCAGCTGCAGCTCAACCTGGCCCACCACGCTGTCCAGAGGCTGCGCGTGTCTCTAGGAGCAACTCGAAAA[C/T]AACTGCCTGAAAATTACGACCCCCGAGAGCTGGTTCAGAACTCTTCTACCGAGCAGCTCCGAACCATCATCAGATATCTACTGGACACACTGCTCAGCCTGCTGCACTCCTGTAATGGTGAGGGAGACGGTCAAACATCAGCTCGCTGTCAAAACCAATTCAGCTTAATCTAAACCTTGAATGTGAATATTATATTCTTCTCTTTTGCACTCTCAGGCAACTCGGTGCCCTCAGTGTTGCAGAACACATTTCATGCTCAGGCGTGCGAGGAGCTCTTTAAGCAGCTGTGCATCAGTGGGACGCCTAAGATTCGTCTGCATGCGGGTCTGCTGCTGGTGCAGCTGTGTGGAGGAGAGAGGTGGTGGGGCCAGTTCCTGTCCAACGTCCTGCAAGAGCTCTATAACTCTGAGCAGCTGCTCATCTTCCCTCAGGACAGGTAACACTACGCTTTAAAAAAGATTATTGCTGCCTTAATTCTTTGATGCAAATACTCTTTTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44872
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114100 | Essential Splice Site | 2103 | 4870 | 31 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22462627)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22612776 |
GRCz11 | 17 | 22632612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAAGAGCTCTATAACTCTGAGCAGCTGCTCATCTTCCCTCAGGACAGG[T/G]AACACTACGCTTTAAAAAAGATTATTGCTGCCTTAATTCTTTGATGCAAA
Long Flanking Sequence:
AGCTCAACCTGGCCCACCACGCTGTCCAGAGGCTGCGCGTGTCTCTAGGAGCAACTCGAAAACAACTGCCTGAAAATTACGACCCCCGAGAGCTGGTTCAGAACTCTTCTACCGAGCAGCTCCGAACCATCATCAGATATCTACTGGACACACTGCTCAGCCTGCTGCACTCCTGTAATGGTGAGGGAGACGGTCAAACATCAGCTCGCTGTCAAAACCAATTCAGCTTAATCTAAACCTTGAATGTGAATATTATATTCTTCTCTTTTGCACTCTCAGGCAACTCGGTGCCCTCAGTGTTGCAGAACACATTTCATGCTCAGGCGTGCGAGGAGCTCTTTAAGCAGCTGTGCATCAGTGGGACGCCTAAGATTCGTCTGCATGCGGGTCTGCTGCTGGTGCAGCTGTGTGGAGGAGAGAGGTGGTGGGGCCAGTTCCTGTCCAACGTCCTGCAAGAGCTCTATAACTCTGAGCAGCTGCTCATCTTCCCTCAGGACAGG[T/G]AACACTACGCTTTAAAAAAGATTATTGCTGCCTTAATTCTTTGATGCAAATACTCTTTTCTAGTCATCTCTACTTACACTACACTAAGTTTGGGGACAATAGGATTTATAAATGTTTAAAAATATGCCTCTCCTGCTCACACATTATTTAATCAAAAATACAGTACAAATTGTAAAATTGTGAAAAAAGTTATTGCACTATAAATAATTGTTCAAAAGTAGTTTATAATTGAATTGAATTTAATTTAATTAATCGTTTAATTTTCCAATGATTTTAAAGATGAATTTTCAGCTTCATTACTCTAGTCTTCAGATTCACATGATCCTTCAGAAATCACTCTAATATGAATTATTATTATTATTATTATTATTATTATTATTATTATGTTGCTTATTATTATTATTTCTATAATTATTATTGTTAATATTATTAATTGTAATAGTAATAAAAGTAATAATGACTGAAGTAATAATTCCATTTGAAACTAAATACAATAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10215
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Essential Splice Site | 2229 | 4870 | 34 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22464941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22615090 |
GRCz11 | 17 | 22634926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGKCTGTATTCAYGCAAGATCCGCAAACAGCTAGWCCATCACAAACAGG[T/C]ACACGTGTCTTGCACAAACCTTTTTATTGTGCTAGGGTTTTTCTATACCR
Long Flanking Sequence:
ACTTCCAGAAATTATATTAAGCTTATTTAGTGTTTAAAGAAATGTTCAATCTTATATCCTAAAAGTGTTGTGGTGATTTAAAAAAGAAAAAAAAAAAAGAAAAAAAACTGAATTACTTTTTTTGAAATCTCAAGATTTTGCTGAATAAGACCAGCTTATATATGATAAGAGAAATTTTGGTAACATTTGAAACCTCTATGCTGTCACTTTTGATCAATTTAATGTGTCCTTAATAAATATATGAATTTATATATTTCAAAAAGTCTTACTAGTAACAAATCTTTGAAAAATTGTATGCATGGTATAGAGAGTTTTTTTTTTTTCTTCTGATGATGCTTACTACACTTTTCTCTTTTCTATGACACCAGGGAACCAGTGGAGTTTTATAAATAACAGTCTGCAGTCTCAGAACCCAAGCAGATCTGCTAAAGGCAGCAACAGCAGTTTAGATCGTCTGTATTCACGCAAGATCCGCAAACAGCTAGTCCATCACAAACAGG[T/C]ACACGTGTCTTGCACAAACCTTTTTATTGTGCTAGGGTTTTTCTATACCGTCACATCAACTTGAAGTCTTTTATTGATATAGAGAGGATGTTAATCAATATTTATTTCATTGCAGCAGTTGAATTTATTGAAAGCCAAACAAAAAGCTTTAGTAGAGCAAATCGAGAAGGAGAAAATTCAGAGCAACAAAGGCTCCTCTTACAAGCTGTTGGTGGAACAGGCCAAACTCAAGCAAGCCACTTCCAAGGTGAGTATCTAGTTATTGGCACTTCATTTTTAAGGCAAGAATTTGTGGCAACAAATATGAAAGAACAAATTCGCAATTATTAACATAGCTTTGAGATGGATCATAATGCTAACCTTGTGGTTATGTGTCTTTGGCAGCACTTTAAAGATCTGATCCGTTTGAGGCGGACAGCCGAATGGCCTCGCTCCACTTTGGACTCTGAAGCGTCAGTGGCAAAAGAGACCCCCGAGGTGGAGCTCCTGCCCTTCACGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17388
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Essential Splice Site | 2345 | 4870 | 36 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22465543)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22615692 |
GRCz11 | 17 | 22635528 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCAATGGACTTCACCTGCCACGCAGACCTGCTCCTGTTTGTTTGCAAGG[T/C]GCAAATTRTWTTATGCATYCCTAAGTCGAGGCTGAMATGMAGGGGTGACY
Long Flanking Sequence:
TTATTTCATTGCAGCAGTTGAATTTATTGAAAGCCAAACAAAAAGCTTTAGTAGAGCAAATCGAGAAGGAGAAAATTCAGAGCAACAAAGGCTCCTCTTACAAGCTGTTGGTGGAACAGGCCAAACTCAAGCAAGCCACTTCCAAGGTGAGTATCTAGTTATTGGCACTTCATTTTTAAGGCAAGAATTTGTGGCAACAAATATGAAAGAACAAATTCGCAATTATTAACATAGCTTTGAGATGGATCATAATGCTAACCTTGTGGTTATGTGTCTTTGGCAGCACTTTAAAGATCTGATCCGTTTGAGGCGGACAGCCGAATGGCCTCGCTCCACTTTGGACTCTGAAGCGTCAGTGGCAAAAGAGACCCCCGAGGTGGAGCTCCTGCCCTTCACGCTAGCTCACGAGCGTTGCATCTGTGTGGTCCAGAAACTTGCTCTTTTCCTCCTCTCAATGGACTTCACCTGCCACGCAGACCTGCTCCTGTTTGTTTGCAAGG[T/C]GCAAATTGTATTATGCATCCCTAAGTCGAGGCTGAAATGCAGGGGTGACCGCGCTTTCCCAGTAGCTGGTCCTACATTGTAGAATGCTCTGCCCCTCTGTATTAGATCTATATTATCTCTGTCTGTTTTTAAATCTATGTCGAAAACTTACCTTTTTGATTTGGCATTTTATCAGTGGGAGTTGTTTGTTTTAGCTATAATTTTATACCTTTCTCTTTGTGATTTGTTTTGTGCAGCACATTGGTCAACCTTTGTTTGTTTAATAGTGCTATATAAATAAAATTGACAAATAAAAATATAATATACCGTATTTTCCACACAATAAGACGCAGCGGATTATAGGCTGCAGTTTCAATTCCGGGGTTTATTTCTGTACTTAACCCATACTCAAGGCACACCACATTATAAGGCGCATGCTAAAACTGGCGTTTATTAATTTTTACATAATTTTTTATAATCAATCTGCTCCTACAAATCCATCAAAGTCCTCATCTTATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23066
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 2355 | 4870 | 37 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22467302)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22617451 |
GRCz11 | 17 | 22637287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGAATGTACTCCAACTACCCAGGTCTTGGCCAGGATAGCAAATGCGACA[C/T]GACCCACGATCCACCTGTGTGAAGTAGTTTCCGAGCAGCAGCTGGAACGG
Long Flanking Sequence:
AGTTTTTTTTTATTATTAATGCTTATTAATCAGAGAGATGCAGCATTAAATATAAAGAATCAGTAATACATCATTGGTTCATTCTATGAGCATATAACAAAATCAATTGACATTTTCTTTCTGTCTGACTCAAACAGTACAATTATAAATGTTAGCATCAAAAGTGATATTTAGCACAGAAACACGAATGATCTAAAACATAATAATAAGATAAATAAAAAGATGCGATACAAATAATTATGCAAGTACAAATCATCTTATTATAAATCTTATTATATCGAAAAATTAAATATAATTTATTTGTATAAAATGTTATTGTTATTCATATATTTTTATAGAATCTGAATGTATATATGTTTGACGGGTTTTGTTTGTTAAAAAAAAAAAAAGAAAATTACAAGCTAAAATATGTAGAAGATTGACCCCCTGTTTTGAACCATTTTTAATGTATCGAATGTACTCCAACTACCCAGGTCTTGGCCAGGATAGCAAATGCGACA[C/T]GACCCACGATCCACCTGTGTGAAGTAGTTTCCGAGCAGCAGCTGGAACGGTTGCTTCTGTTATTGGTGGGGACTGACTTCAACCGCGGGGACATTTCGTGGGGTGGAGCCTGGGCTCAGTACTCCCTCACCTGCATGCTGCAGGATATCCTTGCAGGTTTGTGTTTTAGACCCACGGACAGTCATCCACTCATCATTTATTGATTTGTATTTAGCTGACACTGTATGTGTTTTCAGGAGAGCTGCTGTCTCCGGGGTGTGTGGATGGGATGGAGGGTGCGGGGGCTGATGAGGCCGGGGCCGCCTCTTCCTCTGTAGTGGTGGATTCGGATGACTCTCTCCCTCAGCCGACCCCCATCCCGCTGGTAGAGACCATCGATGAGCCTCTTGGACCTGATATCATCGCAGGTACACCCGGGACATCCTCTGTGTTCCAAAGTGCGTTGGTAACCCCGTCCGAATAGCACATCACCCCACATGGACCCCTTCCCTCACCTGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36396
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 2958 | 4870 | 47 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22477066)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22627215 |
GRCz11 | 17 | 22647051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGCAGGTGGAGCTACTGACAGCGTGTCGGATGAAGAAAAAGTGTGT[G/T]GAAGTAAAGAGTGTGGGGCGGCAGGCACAGCTCAGCATCAGGGACCAGCA
Long Flanking Sequence:
TTTTAAAGGTTTCATGACAGTCTTATGAACACCCTTCAAGTAAAATGAAACCGTATTTTATTTTTACCCTCTTCTCTGTTTGAAGGGGTCCATTCCAGTCCGGTCAGGGTCCTTTAGATGCACAGGTGAAGCTTTTGGAGTTCACCCTGGAACAAAACTTTGAAGTTGTTTCTGTGACCACCATCTTGGCCGTCATCGAATCCATCACCTTCCTGGTTCACCATTACATCACCTGCTCTGATAAGGTGGTCTCACGCAGCGGTTCCGACAGCTCTGTAGGGGCTCGTGCCTGTTTCGGGGGCCTTTTCGCTAATATCATCCGTCCCGGTGATGCTAAGGCCGTGTGTGGTGAGACCACACGAGACCAGCTGATGTTTGACCTCCTGAAGCTGGTCAATGCTTTGGTGATGCTGCCTCTGTCAGGTGATAGGGAGTTCAGCGGGAGGCTTCCTCCAGCAGGTGGAGCTACTGACAGCGTGTCGGATGAAGAAAAAGTGTGT[G/T]GAAGTAAAGAGTGTGGGGCGGCAGGCACAGCTCAGCATCAGGGACCAGCAGCAGGAGTGGCAGATCTGGTTTTGGCCAATCAGCAAATTATGAGTCAAATCCTGTCAGCTCTGGGGCAGTGCAACAGCAGTGCCATGGCCATGATAATTGGTACATCACTTTAATTTGAAATTAATAAATGTAAAATTATATTATATTATATTATATTACATTATATTATATAACATTATATATGAGGAGATTATGTGTAGTTAATTCTATAAAGTAATTCATTACAAAAACATTAAGCAGCACAACTGTTTTCAAAATTGACAGAAATGTTTTTAACCACCAAATCTAGATCTGCAGATGTTTTTTTTTTGATTGGTCATTCAATATTGAAAACTAGAGTAATGTCTGTTGACTTTGTTATCAAATAAATATTTTTTATAACGTTTTTAAATATTAATACAAATGATTAAAATTTATTTTGTAATGCTGTACAGTATATTGTATAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23067
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 3279 | 4870 | 52 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22480651)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22630800 |
GRCz11 | 17 | 22650636 |
KASP Assay ID:
2261-0983.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGTTCCAGCTGGTAAAGGCAGAGGTGGCGTCTGCTGTGTGTCTGAGGT[T/A]GCACCGGCCGCGGGACGCTAGCACTCTTGGCCTCTCGCAGATCAAACTAC
Long Flanking Sequence:
CGGTATACATTATTTCAAAATAAATGTAATTGCAATTTTCTCAGCCATACAACTTTTCTATTTTAAAAATAATGCAAACACAATAATAAACATTATTATTATTATTATTCTATTTTTCTTATTCTTAAAATAATAATAAAAATATTAACATCAACAATTGTTTTAAACAGTTTTGAGAGGTTAGATATATACTTAGTCAAATTTTTTATTAAATAATGTTAAGTGCTGGTTTATGGTCTATGGTAGGTCAGAAGAAGAAGGACATTTGTTTTATTCCTCCGCGAAATCTGTCTGTAATGGCTTTTGCCCTGGAATCGGTTAAATTAGTATTTAATGCTACTCTTTCTTTTCCCTAGCATGTCCATCCTCGGTATCTGTGGAGATCAGCGCAGATGGTGTGAACATGCTTCCCTTGTCGACTCCAGTCATCACGAGTGGTCTCACCTACATCAAGTTCCAGCTGGTAAAGGCAGAGGTGGCGTCTGCTGTGTGTCTGAGGT[T/A]GCACCGGCCGCGGGACGCTAGCACTCTTGGCCTCTCGCAGATCAAACTACTGGGCTTGACTGCTTTCGGAAACACTTCCTCTGCCACTGTAAACAATCCATTCCTGCCCTCTGAGGACCAAGTCTCCAAAACCAGGTATCTGTGTTTTACCAATCGGTGTGTTGAGAAGTTTGATTTCTCATTTTAGACCCAAGTGTATAATAATAATTCAAATTTTTTGCCTGTTTTTTTCAGTATTGGCTGGTTACGGTTGCTGCACCATTGCTTGACTCACGTTTCTGATCTGGAGGCCATGATGGCCAGTGCTGCTGCTCCTACAGCAAACCTCCTGCAGACCTGCGCCGCCCTGCTCATGTCTCCATACTGTGGCATGCACTCGCCCAACATTGAGGCTGTGCTGGTGAAGATCGGCCTGCAGTCCACACGCATAGGTCTTAAGCTCATCGACATCTTACTGCGTAACTGTGCGGCTTCTGGAACGGACTTAGCCAGTAAGACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36397
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 3524 | 4870 | 56 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22483359)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22633508 |
GRCz11 | 17 | 22653344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGGCCACCTGAACTATTAATTCTCTTCAATGTCTTGCAGGTTGTTGTA[C/A]AACTGGTCCATGTCTTTGCCCTCTAACATGGTTTTAAAGAAGGCTGTGGA
Long Flanking Sequence:
GTTGGCCCAATCGCTCCGCCCCCTCGGGAATATGGCTTGCTCATGCCCTCCCCATCACACCTGCACTGTGTGGCATCCGTCTTGTGGCACAGTTATGAGCTGCCTGTGGACTACGACTTGCCCGGCCTACTCAACAGAGAGCTTTTTGAGTGAGTCTGCACAGATAAGCACACTCTCTTTTTGCAGTCACGCAGAACAAAATGTTCAAGTAAGAGTTGTGGATGAGTGCTTGTTTATGCCTGAGGTAAGTTTTTAGTGCTCTGCATCTAGAAAAAACGCTGAGGGTGTATATTGAGCTAGTTCTCTTCATCCTCTCTTCAGGTATGAATACTTTATAGGTACAGAGTAGAACAAAGTGAAACAACCTTCGCCATGTACACGGAGCAAATAAAACACCGGCAGCCGTTAATACTAACAGTTCTGAGCATAAGTTAAACATAAGGATGTTTTTTAGGCCACCTGAACTATTAATTCTCTTCAATGTCTTGCAGGTTGTTGTA[C/A]AACTGGTCCATGTCTTTGCCCTCTAACATGGTTTTAAAGAAGGCTGTGGACAGCTTGCTTTGTTCCATGTGCCACATCCACCCCAATTACTTCTCTCTTCTCATGTCCTGGATGGGTATCGTGGCGCCCTCGTCTGCCCAGACCAACGCGCAGCGCCGGATGGCCATGACCGACGACGGCAAGAAGCAGCATGACTTAAACAGCGCCGCCTCCCTCACCGATGACTCCAAACATGCTCGAACACCAGTAACCGTGCCCATCTCCCTCTCAGAGTGCCAGCTGGTGACCCTTGCAGCTGCATCCCAGTCTCCTGGTGCCATTCAGCAGCTGTTAGACTCCGGTCTGCCTTCCTTGCTGGTGCGTAGCTTGGCTGACCTTTGCTGCAACCTGTTGGTCAGCGCGGATCTTCCTTTACCTTCAGGATTCTCCTCACAGACCGAGAGACGGCCGTATTCACATAACCAACACTCACCTTCCTCCACCAACAGGCCGCCTTTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2916
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 3575 | 4870 | 56 | 76 |
ENSDART00000114100 | Nonsense | 3575 | 4870 | 56 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22483510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22633659 |
GRCz11 | 17 | 22653495 |
KASP Assay ID:
554-3056.1 (used for ordering genotyping assays)
KASP Sequence:
TCATGTCCTGGATGGGTATCGTGGCGCCCTCGTCTGCCCAGACCAAYGCG[C/T]AGCGCCGGATGGCCATGACCGAMGACGGCAAGAAGCAGCATGACTTAAAC
Long Flanking Sequence:
GAGTCTGCACAGATAAGCACACTCTCTTTTTGCAGTCACGCAGAACAAAATGTTCAAGTAAGAGTTGTGGATGAGTGCTTGTTTATGCCTGAGGTAAGTTTTTAGTGCTCTGCATCTAGAAAAAACGCTGAGGGTGTATATTGAGCTAGTTCTCTTCATCCTCTCTTCAGGTATGAATACTTTATAGGTACAGAGTAGAACAAAGTGAAACAACCTTCGCCATGTACACGGAGCAAATAAAACACCGGCAGCCGTTAATACTAACAGTTCTGAGCATAAGTTAAACATAAGGATGTTTTTTAGGCCACCTGAACTATTAATTCTCTTCAATGTCTTGCAGGTTGTTGTACAACTGGTCCATGTCTTTGCCCTCTAACATGGTTTTAAAGAAGGCTGTGGACAGCTTGCTTTGTTCCATGTGCCACATCCACCCCAATTACTTCTCTCTTCTCATGTCCTGGATGGGTATCGTGGCGCCCTCGTCTGCCCAGACCAACGCG[C/T]AGCGCCGGATGGCCATGACCGACGACGGCAAGAAGCAGCATGACTTAAACAGCGCCGCCTCCCTCACCGATGACTCCAAACATGCTCGAACACCAGTAACCGTGCCCATCTCCCTCTCAGAGTGCCAGCTGGTGACCCTTGCAGCTGCATCCCAGTCTCCTGGTGCCATTCAGCAGCTGTTAGACTCCGGTCTGCCTTCCTTGCTGGTGCGTAGCTTGGCTGACCTTTGCTGCAACCTGTTGGTCAGCGCGGATCTTCCTTTACCTTCAGGATTCTCCTCACAGACCGAGAGACGGCCGTATTCACATAACCAACACTCACCTTCCTCCACCAACAGGCCGCCTTTGTCTCCTGAGCTCGCGGCTCCGGTTTTGCGCTTTCTTACAGAAGTAGGAAACAGTCACACCATGAAGGACTGGCTGGGTGGCCCGGAGGTAAACCCGCTCTGGACGGCGCTGTTGTTTCTTCTGTGCCACTCGAGTGCTAGTGGGACTGCTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13557
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 3626 | 4870 | 56 | 76 |
ENSDART00000114100 | Nonsense | 3626 | 4870 | 56 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22483663)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22633812 |
GRCz11 | 17 | 22653648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCCATCTCCCTCTCAGAGTGCCAGCTGGTGACCCTTGCAGCYGCATCY[C/T]AGTCTCCTGGTGCCATTCAGCAGCTGYTAGACTCCGGTCTGCCTTCCTTG
Long Flanking Sequence:
CTTCATCCTCTCTTCAGGTATGAATACTTTATAGGTACAGAGTAGAACAAAGTGAAACAACCTTCGCCATGTACACGGAGCAAATAAAACACCGGCAGCCGTTAATACTAACAGTTCTGAGCATAAGTTAAACATAAGGATGTTTTTTAGGCCACCTGAACTATTAATTCTCTTCAATGTCTTGCAGGTTGTTGTACAACTGGTCCATGTCTTTGCCCTCTAACATGGTTTTAAAGAAGGCTGTGGACAGCTTGCTTTGTTCCATGTGCCACATCCACCCCAATTACTTCTCTCTTCTCATGTCCTGGATGGGTATCGTGGCGCCCTCGTCTGCCCAGACCAACGCGCAGCGCCGGATGGCCATGACCGACGACGGCAAGAAGCAGCATGACTTAAACAGCGCCGCCTCCCTCACCGATGACTCCAAACATGCTCGAACACCAGTAACCGTGCCCATCTCCCTCTCAGAGTGCCAGCTGGTGACCCTTGCAGCTGCATCC[C/T]AGTCTCCTGGTGCCATTCAGCAGCTGTTAGACTCCGGTCTGCCTTCCTTGCTGGTGCGTAGCTTGGCTGACCTTTGCTGCAACCTGTTGGTCAGCGCGGATCTTCCTTTACCTTCAGGATTCTCCTCACAGACCGAGAGACGGCCGTATTCACATAACCAACACTCACCTTCCTCCACCAACAGGCCGCCTTTGTCTCCTGAGCTCGCGGCTCCGGTTTTGCGCTTTCTTACAGAAGTAGGAAACAGTCACACCATGAAGGACTGGCTGGGTGGCCCGGAGGTAAACCCGCTCTGGACGGCGCTGTTGTTTCTTCTGTGCCACTCGAGTGCTAGTGGGACTGCTAATGCAAACAGCAGCAGCAGCAGTGTTTGTGGGCATGGAGCATCGCCCAGCACTTCACACGCCAGCGCTGCACCTCACACATCAGGTGCGTCATACTCACTGGCGTCATCAAGCCGCAGTAGTGGACTCACCACACAGCAGAGGACCGCCATCGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13763
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 3626 | 4870 | 56 | 76 |
ENSDART00000114100 | Nonsense | 3626 | 4870 | 56 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22483663)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22633812 |
GRCz11 | 17 | 22653648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCCATCTCCCTCTCAGAGTGCCAGCTGGTGACCCTTGCAGCYGCATCY[C/T]AGTCTCCTGGTGCCATTCAGCAGCTGYTAGACTCCGGTCTGCCTTCCTTG
Long Flanking Sequence:
CTTCATCCTCTCTTCAGGTATGAATACTTTATAGGTACAGAGTAGAACAAAGTGAAACAACCTTCGCCATGTACACGGAGCAAATAAAACACCGGCAGCCGTTAATACTAACAGTTCTGAGCATAAGTTAAACATAAGGATGTTTTTTAGGCCACCTGAACTATTAATTCTCTTCAATGTCTTGCAGGTTGTTGTACAACTGGTCCATGTCTTTGCCCTCTAACATGGTTTTAAAGAAGGCTGTGGACAGCTTGCTTTGTTCCATGTGCCACATCCACCCCAATTACTTCTCTCTTCTCATGTCCTGGATGGGTATCGTGGCGCCCTCGTCTGCCCAGACCAACGCGCAGCGCCGGATGGCCATGACCGACGACGGCAAGAAGCAGCATGACTTAAACAGCGCCGCCTCCCTCACCGATGACTCCAAACATGCTCGAACACCAGTAACCGTGCCCATCTCCCTCTCAGAGTGCCAGCTGGTGACCCTTGCAGCTGCATCC[C/T]AGTCTCCTGGTGCCATTCAGCAGCTGTTAGACTCCGGTCTGCCTTCCTTGCTGGTGCGTAGCTTGGCTGACCTTTGCTGCAACCTGTTGGTCAGCGCGGATCTTCCTTTACCTTCAGGATTCTCCTCACAGACCGAGAGACGGCCGTATTCACATAACCAACACTCACCTTCCTCCACCAACAGGCCGCCTTTGTCTCCTGAGCTCGCGGCTCCGGTTTTGCGCTTTCTTACAGAAGTAGGAAACAGTCACACCATGAAGGACTGGCTGGGTGGCCCGGAGGTAAACCCGCTCTGGACGGCGCTGTTGTTTCTTCTGTGCCACTCGAGTGCTAGTGGGACTGCTAATGCAAACAGCAGCAGCAGCAGTGTTTGTGGGCATGGAGCATCGCCCAGCACTTCACACGCCAGCGCTGCACCTCACACATCAGGTGCGTCATACTCACTGGCGTCATCAAGCCGCAGTAGTGGACTCACCACACAGCAGAGGACCGCCATCGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39160
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 3652 | 4870 | 56 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22483743)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22633892 |
GRCz11 | 17 | 22653728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTCCGGTCTGCCTTCCTTGCTGGTGCGTAGCTTGGCTGACCTTTGCTG[C/A]AACCTGTTGGTCAGCGCGGATCTTCCTTTACCTTCAGGATTCTCCTCACA
Long Flanking Sequence:
CAAATAAAACACCGGCAGCCGTTAATACTAACAGTTCTGAGCATAAGTTAAACATAAGGATGTTTTTTAGGCCACCTGAACTATTAATTCTCTTCAATGTCTTGCAGGTTGTTGTACAACTGGTCCATGTCTTTGCCCTCTAACATGGTTTTAAAGAAGGCTGTGGACAGCTTGCTTTGTTCCATGTGCCACATCCACCCCAATTACTTCTCTCTTCTCATGTCCTGGATGGGTATCGTGGCGCCCTCGTCTGCCCAGACCAACGCGCAGCGCCGGATGGCCATGACCGACGACGGCAAGAAGCAGCATGACTTAAACAGCGCCGCCTCCCTCACCGATGACTCCAAACATGCTCGAACACCAGTAACCGTGCCCATCTCCCTCTCAGAGTGCCAGCTGGTGACCCTTGCAGCTGCATCCCAGTCTCCTGGTGCCATTCAGCAGCTGTTAGACTCCGGTCTGCCTTCCTTGCTGGTGCGTAGCTTGGCTGACCTTTGCTG[C/A]AACCTGTTGGTCAGCGCGGATCTTCCTTTACCTTCAGGATTCTCCTCACAGACCGAGAGACGGCCGTATTCACATAACCAACACTCACCTTCCTCCACCAACAGGCCGCCTTTGTCTCCTGAGCTCGCGGCTCCGGTTTTGCGCTTTCTTACAGAAGTAGGAAACAGTCACACCATGAAGGACTGGCTGGGTGGCCCGGAGGTAAACCCGCTCTGGACGGCGCTGTTGTTTCTTCTGTGCCACTCGAGTGCTAGTGGGACTGCTAATGCAAACAGCAGCAGCAGCAGTGTTTGTGGGCATGGAGCATCGCCCAGCACTTCACACGCCAGCGCTGCACCTCACACATCAGGTGCGTCATACTCACTGGCGTCATCAAGCCGCAGTAGTGGACTCACCACACAGCAGAGGACCGCCATCGAGAATGCCACAGTGGCTTTCTTCCTGCAGTGCATCTCCTGCCATCCAAACAACCAGAGGCTCATGGCACAGGTGTGTTTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45604
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 3885 | 4870 | 59 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22488276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22638425 |
GRCz11 | 17 | 22658261 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGCAAACTGCATCTGCCCATCTCAACTACACTATCAGAAGTATTGGAC[C/T]GAGTCTCAGGTATGGATACACTGCTATTCAAAAGGTTTGGTTAGTAAAGC
Long Flanking Sequence:
AAGGTGTACCAATTAAAAATGGCCTACTGATGTTTTGCTTTTATATTTTTATATAAGGCTATTATTTGTGCATAAGTATATCTAGATAAAGTAATAAACATACAGTTCGTTTGAATAATTTTATAATACCTACTGCTAACTTATGAGTGATATCATCATTAGATGTGGAGGGGGGCCTTAAAATATTTTTATGGGGAAATGGGGGGTCTCAGGCAAAAAAGGTTGGGAACCACTGTATTATGAGACATTAAAAATATCATAATAAGGACACTAAGATATATGTTAAAGTGCAATATCATCCTAATGCAACTTTTTACTGTATAATAGGTTTGCACACTGCTAAGGTGACCCGTCTCTGTTTTTCTTTTTCTCTGCCTCAGCTTTATAAAGGGCGCATTAATGCCACAAGTCATGTGATCCAGCACCCCATGTACGGAGCAGGGCACAAGTTTCGCAAACTGCATCTGCCCATCTCAACTACACTATCAGAAGTATTGGAC[C/T]GAGTCTCAGGTATGGATACACTGCTATTCAAAAGGTTTGGTTAGTAAAGCTTTTATTTTTAAATAAGTTAGCAATTCAGTTGATCAAAAATGACTGTAAAGACATTTATAACATTTATAGACGTTAATATTTGTAAATAAACAATGATTTGATCTTTTATCTTGAAAACAAAAAGGTTTTACACTTATTAATTCACGGTTTTCAGCACTGATAATGTGAATTGTTTCCTGAGTACAAAATCCACACCAATGTTTTTTTTTATATCAAATAAAAACAAATTTATTTGATTTATTAAAAAAATAATTGTAGACAATTGATTTAACATTTTTAGTACCATTGAGATCATTCACATTAGCCATTTAATTCACAAAACATTTTCCCTTGATCAGGTTGAATGAATTTCCATCAGTCATACAGTGAGCTAGTTTTGCATGGAGCCTGCAGTAGTCTATCAGATCTATTAGATTCAGCTTTTGCTACATCTTCAGACTTTCAAGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8438
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 3900 | 4870 | 60 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22489219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22639368 |
GRCz11 | 17 | 22659204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTAACCCTTTAGATACACCKAGCATCACAGCAAAACTGATCAATGAA[C/T]ARAAGGAGGATAAAGAGAAGAAAAACCATGAGGAAAAGGAAAAGATGAAA
Long Flanking Sequence:
AGTAGTCTATCAGATCTATTAGATTCAGCTTTTGCTACATCTTCAGACTTTCAAGGTCTGATGCACAAAGCATGTAGGGCTAAAACTGTCATGTGGCATGGTCATCAGCATGTGTGTGTGATGAATTGCTTGTCGCTTGAGACCTTGAGTGTGGCAGATATAGTCTTAGTTTCCTCTGAAGACTTCAAGATACATCGTACATAAGGTGTCCTGTCTCGGAGCTGTTCTCGTGCTTGCATCACTTCCATAGATGGAAGACCCTCATAGGAAGCACAGCAGGTCGTTATCGTTATGGATTGCTGTTTCTTCATGGGCATATTACATCTTTACTTTCAGATATTCAGATTATCAGTTAAAATGACATGTTGTTCGTTGCATATGTCTCTAAAGGGAAATGTATTTTTCGAGCCTGCAGGCTGACTGCACACATACTGTGAGATAACTTGGTATTTTTTAACCCTTTAGATACACCGAGCATCACAGCAAAACTGATCAATGAA[C/T]AGAAGGAGGATAAAGAGAAGAAAAACCATGAGGAAAAGGAAAAGATGAAAGCTGATAACGGTTTCCAAGACAACTACAGTGTCGTTGTTGCCTCAGGTACTGTTTAACCCTGCATTGAATCACTGAAAATCACCCTGCATTGCATCACTGAAAGTTTCCTATCACTGCATGCCGTTAACAAGAATATGGAAAAATACTAACAGCCTACTAGTGCAACCATCTAACAACCATCAACGAACTACCTAAAAAAAACTCAAGCATTATAACACTGTGCCAGCCACCTGAAACATCTTAGCAACCAGATAACAACCAACAAGATTCCGCTTTCATCGTCTTACAGCAACCCTTGCCACCTATAAAAAACCCAAAACAAATGAACCCAAAATTCATTTAGAGATATCTCTAATTACAATTGTGACTAGTCAAAACTCATTTAGAGATATCTGCAAATATTTTTCAATGGAAGTCAATGGAGGAATATGACTAGTCATAATATATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17275
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Nonsense | 4047 | 4870 | 63 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22498986)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22649135 |
GRCz11 | 17 | 22668971 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGATTGAATGATGCATTTCTGGGCTTCTTTCGTCCTGTAGATCACTGC[G/T]AGATGCTAAGCGGCTGTCCTGACGATGAACCGATGACCCCRGGTGACGAG
Long Flanking Sequence:
TACAGATTATACACGTACAAACAAGTAAAATGGGGAAAAGTCTTGATTAAATCCAAACACACAGGGTGGAAACTGACACATCTCAGCTCACCATTTGTGATCAGATCTTCAAAAGAGCATATTAATACCAGATGTGAATAGGGCCGTTATGTCAGCTGTAAACTCTATAAATCTGCTCCGTGTTTATATTAGAGCACTGTTGTTTCATTACAATTCTGACTGTGCATTCAGAAACACTTAACAGCCAATATCTCCTGCAACTTTCTCCTTATTCCCTCACATCGATCCTCAATCTCAGCAAATGAAAACCTGATTTAGAGGAATAATCTGATTTATGAGAACAGAAATGAGCTCTTGTGCAGTACTGCCCTGCTTTGGACATCGTGGTTTATGATGGGAACAATTGAGACCACTTTATTTACAGCTAGACGTTATGAGATTTTATTGACGCCAGATTGAATGATGCATTTCTGGGCTTCTTTCGTCCTGTAGATCACTGC[G/T]AGATGCTAAGCGGCTGTCCTGACGATGAACCGATGACCCCGGGTGACGAGGGTTTGGATGCTGCGGTGGATGACAGCCTCCTGGAGACCAGTCCTATCCAGTCTCCTTTGCAGGTGTTCGCCGGTATGGGCGGCTTGGCGCTGATCGCGGAGAGACTTCCAATGCTGTACCCCGATGTCATCCAGCAGGTCAGTATATCTGCAAGCTTGCTCTCTGTGCAAAATTATATTCTACCGCGTAGGTAATTTTATGTAGTTTCACTTCATTTCTGCTTCATAAGCCACTCGTTCGCTGACCGTAACCTGAGGTTAGTCAGCATTTCTGTTCATTTGCGTGTCCTCTGAGCCAGTTCGTCCGGATCGTTCTGTGCAGGTCAGTGCCCCAGTGGTGCCATCCACCACACAGGAGAAACCCAAGGACAGCGACCAGTTCGAGTGGGTCACTATTGAACAATCCGGAGAGCTTGTTTATGAGGCGCCCGAGACTATTGCGGCCGAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36398
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Essential Splice Site | 4282 | 4870 | 65 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22503508)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22653657 |
GRCz11 | 17 | 22673493 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGCCATCATGCTCCCAGAGTGCCCAGCGGCAGTGCCAACTCCAGTGAG[G/A]TCAGTGTTAACCCGCACGCTGTTTACCTGTCATTCAGCCCACAAAAATCA
Long Flanking Sequence:
AAATCAAGTTTTTATATAGCACTTTTCTCCAATTATATTATAATCAAGTTCAGAAAAGTTAAGCTTATTAGTTACCTTAATGTTATTAGTTACTAATAACTTTAACTAATTAACTGTTTAGTCAGTGAAACCAAAATAAACTCTTTTTAGGAAACGAAAAGTCAGTGTTTTTGACATTTGTCTTAGAGCAGGAACCCTGGGTTTTTCTTGCTCTAAATGTTAAAGACATTCTCATCTAGAAAGACAATTTCTCATTCTATTCATCTGTCATTCTTCCTCAAGGTCACATCCTACAGTCTCCCTCTGCTAACGTTCTACCCACGTTGCCCTTCCACGTGCTTCGCTCCTTGTTCAGTTCTACTCCCCTCACCACGGATGATGGGCTGCTGCTGAGACGCATGGCACTGGAGATCGGTGCCATCCACCTCATCCTGGCCTGCCTGTCTGCCCTCAGCCATCATGCTCCCAGAGTGCCCAGCGGCAGTGCCAACTCCAGTGAG[G/A]TCAGTGTTAACCCGCACGCTGTTTACCTGTCATTCAGCCCACAAAAATCAGCATGTTCGTGACAGCAATGAAAACATTAGCATGTGAACTTGCATGTTAAAACACTCAGTGTTTAGCAAACCAAATAATGACTGAATTCACAGAGTTTGGAGAAGTTTGGAAGGAAAATTATTTGCATATATTTTAAAATGTATTCCTGTGTTGGCAGAGCTGAATTTTTAGCAGCCATTACTAAAAGGAAACAAACAGTAACAAACTGTATCTTGTTATCTTGTATTCAGAGCGAGTTGTCTGTTATTTGGAAAAAAAAATTATGTAAAGCTAAATTATTTTATAAAGACTGACCTGAGTAGTTTGCAGAGTTATTAAAAGAGCATTACAGATGGTGTGAAATGAGATCAGTCCACTAGTAAGTCTTGTTATCTAATGGGGTATATGCACATAGTCAGCCAGCCCAACAACTTCCGATAAACTGTCTTCCCATTACAAAACCGCCCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12006
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 |
---|---|---|---|---|---|
ENSDART00000114100 | Essential Splice Site | 4393 | 4870 | 67 | 76 |
Genomic Location (Zv9):
Chromosome 17 (position 22509489)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 22659638 |
GRCz11 | 17 | 22679474 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTCCTGTCTAATCCCTGCCATGWCTTCATACTTGCGCAATGACTCAGG[T/C]AAGACACGTGTCACATGTGAAATGYATTCAGTGCTTGACTTCTTGCAGAA
Long Flanking Sequence:
TGGTCCGTTTCACACAACTTGATCTTAGTACTGCTTGTGAACAGCATCCACATTGCCAAATCTACAGCTTAGTTTGTGTTTGTGCTGCAGCCGCAGGTCTCCAGTGGGCATGTTGGTGGTACCACAGAGGAACAGCAGCTGTATTGGGCCAAAGGAACAGGCTTTGGGACTGGCTCAACAGCATCAGGCTGGGATGTAGAGCAGGCTCTGACCAAACAACGCCTGGAGGAAGAGCACGTCACCTGCCTCTTACAGGTGTGTGTCTGTTAAAATATATCAATTAAGGTTAAAATTTGCACATGCTTGAATGTGTGATGATATGTTCTGTGTCAGGTTTTGGCAAGCTATATCAACCCATCAGGCTGCGTGGGATCTGGTGAGACCCTCACAGGAGAGGTCAGAGGTCACAGCAGCTCACTGCTGCCATCTGTCCTGCAGGAACTGCTCAGCCAGTCCTGTCTAATCCCTGCCATGTCTTCATACTTGCGCAATGACTCAGG[T/C]AAGACACGTGTCACATGTGAAATGTATTCAGTGCTTGACTTCTTGCAGAACTGCACTTACAAGGTGGCTTAGGAAGATTTCTACATGGCGCTTTAAATTTGTGGTTTTGTCTTTGGAGAAATGTGTTTTTCATCTCTGGTTTGTAGCTATGTCTGTGCAATGTTAGCATCATGGTGTTATGTGTGTTAGTGTTATTATTATGAAGAACCCTTTTCTAGTTTTAACTTTGTATCTAAAGTTTGTATCTCAGTTAATATGAACTCATAAAACTCAGTACTTCCATTGTAATTAGAGCCATGAACAAACACTGCTTTGTTGGTTTAGGGAGCCAGACATTGGTGTGTGTCTGTTGTGCATTCAATGTGTGTGTGTGTGTGTGTGTGTACACACTGTGAGTGTTTATTTCTCTCCGGCTTAATTAAATAAGCGCAGATAAAACGATGAGTGTAGTAATTAGCTCTAGATATCAGCTGGAGGTTTCAACCCTACATTGGCATGGT
Associated Phenotype:
Not determined