ZMP
syne2b
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens SYNE1, spectrin repeat containing, nuclear envelope 1 (SYNE1) [So
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 48 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42265 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42264 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22358 | Nonsense | Available for shipment | Available now |
sa31955 | Essential Splice Site | Available for shipment | Available now |
sa28173 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8900 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42263 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31954 | Nonsense | Available for shipment | Available now |
sa42262 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22357 | Nonsense | Available for shipment | Available now |
sa16388 | Nonsense | Available for shipment | Available now |
sa42261 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa28172 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11835 | Essential Splice Site | Available for shipment | Available now |
sa13694 | Essential Splice Site | Available for shipment | Available now |
sa42260 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31953 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16245 | Nonsense | Available for shipment | Available now |
sa35561 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35560 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22356 | Nonsense | Available for shipment | Available now |
sa42259 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2693 | Essential Splice Site | F2 line generated | Not yet available |
sa8449 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa19067 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9847 | Nonsense | Available for shipment | Available now |
sa38966 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42258 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16713 | Nonsense | Available for shipment | Available now |
sa42257 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7376 | Missense | Mutation detected in F1 DNA | Not yet available |
sa11394 | Essential Splice Site | Available for shipment | Available now |
sa31952 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38965 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22355 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6326 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8857 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22354 | Nonsense | Available for shipment | Available now |
sa22353 | Nonsense | Available for shipment | Available now |
sa9190 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42265
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 36 | 9778 | 3 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | Nonsense | 8 | 281 | 1 | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37652055)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37128867 |
GRCz11 | 13 | 37254757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGTTTTCACTCTCTGCTCTTCCCTCAGTGGAGCAGGAACAAATTCAG[A/T]AGAGAACCTTCACCAACTGGATTAATGCCCAGCTGTCTAAGGTGAGGGTC
Long Flanking Sequence:
GGCTTTTAATAATGTATTAATAAATATTGAGCTCTGATTAAGTACACTGTAAAACCCAAAAAGTTAAGATAACTCAAACCATTTGAGGAAACCGATTGCAACAAACCATTTAAGTTCAGAAACGAATCCTAATGAGTACTGTTAACACAATCCATTTGAGTAATGAAGCAATTTGAGCACAGTAAAACCTAGTAAAAACCAGTCTTTTCTAAACCAGTCTATTCTAAAACCCTAGTAAACCAGTTTATTCATAGACTGAGCAAATTCAGTTAAATGCAGCTCACAGAGATTCAGTTTGAACAATATTATGATTATATAATCTAATATATTATATAATTATATAATCTAATATATAATATATAATCTAATATATAATCATTATATAATCATTATATTGTATAATTAACAATATAAGGATTATTCGCTCATTATGACTGTATGAACTGGGTTTCATGTTTTCACTCTCTGCTCTTCCCTCAGTGGAGCAGGAACAAATTCAG[A/T]AGAGAACCTTCACCAACTGGATTAATGCCCAGCTGTCTAAGGTGAGGGTCAAAGTTCAACCGCTCCTAAACCTGATTTAGAAACCCTACAGCCCTGTTAGAGTGTGTTATGTAATCGCCATGAACTTCATTTGCTATATTTTGAGTTATTTGTTCTGACTGACAAATAACACTTTTTAAAATGCATTTAAACTACAGATTAATGACACACATGGAAATGCTTGTTGGCCGAGGTCATTCCTGACCATTCTCCAATAGCGCAGGGGGAATGAGGGGTGGGCAGGGGGTAAATATAATCTCCTCAAACATGAGCCAGAAAGATAGACAGCAACAGGAGTTGTTCAGCGCACACATTCACCAGCACACATATTCACACCCACAGCTACTTATAAAGTGAGCAAATGACAAGACATGACTGGGACGGGTGTGTATTGTGAAGTAAAGCACGTCAGGGCGTTATTATTTTGGATAGCTTCATATGTTTGTCTCTTCCTCCACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42264
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 131 | 9778 | 6 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | Nonsense | 102 | 281 | 4 | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37647123)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37123935 |
GRCz11 | 13 | 37249825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTCGGATATCATGGATGGCAAACCATCCATCATTTTGGGTCTGGTCT[G/A]GACAATTATCATGCACATTCATGTAAGTTTACTCAATATTAATATTAAGA
Long Flanking Sequence:
ATATTAATAAAGTAAACTTATTTTCTAATAATAAAATACAACCTTTATTTCAGAGCCGAGAGAAAAGAAGAGGGACATTTCAGCACAGATCTAACATTGAGAAAGCTCTAGCGTTCCTTAAGAAGAAATCGGTAAGATGCACCAGCTATTGAAACTCAGGAAAAAAGTAACAATACATTTCAAAGGATGTTTACAGTCTTCTGTTTTTCCTCCCAAATTAAAAGAGCTCAGTTTGTAAGGGAGAGAACTTAAATATAATTGTGTGCATTCCATTTTAATTGCAAAAATATGTTTATGAAATCCTTTTTTATTGAAAAATCAATTATATTAGTTTGTTCAGGCTTGGGGTGTTTTCTGTTTAGTGTGGATAAATATATAATAATAAATGTTGAAATTAGGTGTAAACATCATTGTCCCATATATACTGTAGATCAAACTTGTCAACATCAATGTCTCGGATATCATGGATGGCAAACCATCCATCATTTTGGGTCTGGTCT[G/A]GACAATTATCATGCACATTCATGTAAGTTTACTCAATATTAATATTAAGATTTCATTATTTATAAATACAAACACTCATGGTGAGTAATTGTCAGTTTTGGTGTTTGATTTTTCTGCTGTGTCTTCTATATTGTTTAGATTGAAGAATTGGCCAGCACATTGTCCTTCAGCTCCCGTCAGTCTTCTCTGGAGTCGCTGGCGAGTTTGGACACTCGTTCGACCAACAGCAGTGCCCGCAGCAGTCCAGTGCCACCCCGTGGTTCACCCTTACATGCCCGTTTTCGCGTATCAGCCAAGAAAGCCCTGCTGCTGTGGGTCAGAGAGCAGTGCCAGCGGTGAGGAACAATCTGCTTCAATAAATTGATGGGAACGGACAAATTCTGAACCTGTACTGTGAAACCTATCATCTCATGTTTGTTTTTTCTCAGGGCTGGATGTACTCTGAATGTGAAGGATTTCAAGGTGAGCTGGAGGAGTGGAGTTGTGTTTTTGGCGATACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22358
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 242 | 9778 | 8 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | Nonsense | 213 | 281 | 6 | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37646582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37123394 |
GRCz11 | 13 | 37249284 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCGATACTTCATGCTCTAAGGCCAAATATAGTTGACCTAACCAGAGCT[C/T]GAACAAGAACAAACAGACAAAACCTGGAGGAAGCCTTCCACATTGCTGAG
Long Flanking Sequence:
AATATTAAGATTTCATTATTTATAAATACAAACACTCATGGTGAGTAATTGTCAGTTTTGGTGTTTGATTTTTCTGCTGTGTCTTCTATATTGTTTAGATTGAAGAATTGGCCAGCACATTGTCCTTCAGCTCCCGTCAGTCTTCTCTGGAGTCGCTGGCGAGTTTGGACACTCGTTCGACCAACAGCAGTGCCCGCAGCAGTCCAGTGCCACCCCGTGGTTCACCCTTACATGCCCGTTTTCGCGTATCAGCCAAGAAAGCCCTGCTGCTGTGGGTCAGAGAGCAGTGCCAGCGGTGAGGAACAATCTGCTTCAATAAATTGATGGGAACGGACAAATTCTGAACCTGTACTGTGAAACCTATCATCTCATGTTTGTTTTTTCTCAGGGCTGGATGTACTCTGAATGTGAAGGATTTCAAGGTGAGCTGGAGGAGTGGAGTTGTGTTTTTGGCGATACTTCATGCTCTAAGGCCAAATATAGTTGACCTAACCAGAGCT[C/T]GAACAAGAACAAACAGACAAAACCTGGAGGAAGCCTTCCACATTGCTGAGAGAGAACTTCATATACCCAGACTGCTAGATCCAGCAGGTAAGTCTGTTAGGCCTTGAAAATGTATGCTTTGTATATGCAGTATATCAATCAAACAGCAGTTGTATATTTGTATTTCAGATGTTGATGTTAGAGATCCTGATGAAAAGTCTATCATGACTTACGTTGCTCAGTTCCTGCAGTATTCTAAAGATGCTTCAGTTTCTGATGAAGAAATGCAGGTTAGATACACACACACGTTTTATTGGTGGTTTACGAAGACTTTGCATAGGCATAATGTATTTTATGCCATAAAAACATCTTGTTATATGGCCTTACCTCACCCCTACCCCTAAACCTAAAATGACAGGAAACCTGAGGCAAAATTTGAATGTGAAAAGACACCATTAAGTATTTAAGCATTTTGAATTATGAGGACACAAGGCATGTCCTCGTAAATCACCTTAATGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31955
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 270 | 9778 | 8 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | Essential Splice Site | 241 | 281 | 6 | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37646494)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37123306 |
GRCz11 | 13 | 37249196 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACATTGCTGAGAGAGAACTTCATATACCCAGACTGCTAGATCCAGCAG[G/A]TAAGTCTGTTAGGCCTTGAAAATGTATGCTTTGTATATGCAGTATATCAA
Long Flanking Sequence:
TATTGTTTAGATTGAAGAATTGGCCAGCACATTGTCCTTCAGCTCCCGTCAGTCTTCTCTGGAGTCGCTGGCGAGTTTGGACACTCGTTCGACCAACAGCAGTGCCCGCAGCAGTCCAGTGCCACCCCGTGGTTCACCCTTACATGCCCGTTTTCGCGTATCAGCCAAGAAAGCCCTGCTGCTGTGGGTCAGAGAGCAGTGCCAGCGGTGAGGAACAATCTGCTTCAATAAATTGATGGGAACGGACAAATTCTGAACCTGTACTGTGAAACCTATCATCTCATGTTTGTTTTTTCTCAGGGCTGGATGTACTCTGAATGTGAAGGATTTCAAGGTGAGCTGGAGGAGTGGAGTTGTGTTTTTGGCGATACTTCATGCTCTAAGGCCAAATATAGTTGACCTAACCAGAGCTCGAACAAGAACAAACAGACAAAACCTGGAGGAAGCCTTCCACATTGCTGAGAGAGAACTTCATATACCCAGACTGCTAGATCCAGCAG[G/A]TAAGTCTGTTAGGCCTTGAAAATGTATGCTTTGTATATGCAGTATATCAATCAAACAGCAGTTGTATATTTGTATTTCAGATGTTGATGTTAGAGATCCTGATGAAAAGTCTATCATGACTTACGTTGCTCAGTTCCTGCAGTATTCTAAAGATGCTTCAGTTTCTGATGAAGAAATGCAGGTTAGATACACACACACGTTTTATTGGTGGTTTACGAAGACTTTGCATAGGCATAATGTATTTTATGCCATAAAAACATCTTGTTATATGGCCTTACCTCACCCCTACCCCTAAACCTAAAATGACAGGAAACCTGAGGCAAAATTTGAATGTGAAAAGACACCATTAAGTATTTAAGCATTTTGAATTATGAGGACACAAGGCATGTCCTCGTAAATCACCTTAATGGAGTACAACTAGGTAATACCTTGGTCATTATACAAATTTCTGTCCTTGTAAACCACCAAAACCAGTACACACACACAGACACTGACACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28173
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 382 | 9778 | 12 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37640495)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37117307 |
GRCz11 | 13 | 37243197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTACATTTGTTTCAGGTTTTTCATACCTTTATTGTGTCATTTAATGAA[C/T]AACGCCGGCCCGTGATGCCACTTTTAACAGCAATGAAGAGGACACCCCAA
Long Flanking Sequence:
TACTTATTTATTTTTATAATTTTTATAATTATTAATAGTTTTTTTATTTTATTAATTCATTTATTTAACTTAATTTAGCTTTATTTTAATGAGTTTAGTTTTGTTTAGTTTTTTTATTATTATTTTTATTTAATTTTTATTTAATTTAATTTTATTCATTTATTTTATTATTTGTTTTTATTTGATTTTATTTAGTTTTATTTTATTATTATTTATTTTTTATTTCATTATGATTTAATTAATTTTAATAGTTTTATTTATTTTTATTTTTATTCATTTATTTATTTTTTATATATATATTTAATCTTGTTTACCAATGCTTTGCTTCTGAATTTTGTTATATAATCACATTTTTATACCTGTTATGTCATATTGACAGTGATGAGAATGAAATGTACACATTTGCATTGGTTTTGTTGTACGCGATGATTTATTTTTGCATTAATGTTTATTTACATTTGTTTCAGGTTTTTCATACCTTTATTGTGTCATTTAATGAA[C/T]AACGCCGGCCCGTGATGCCACTTTTAACAGCAATGAAGAGGACACCCCAACTCAGTGCTGAGCAGAAAGCTCTCAGAAGATCATGGGACACTCTCGCTGAAAAGGTCAGAGGTCAAAACAAAAATGCATGCACTTAGCATTTAGAGAACAGAAATGCATAGACATCTTATGCTAATTTGTACTGATGTGTGCATCTATGGTAGCTGCGTGAGTACAAAACAGAGCTGGACCTGACTCTCCCATCACCGCTGGACACTGTGGGCCGCTGGTTGTTGCGTATTGAAGAGGTTTTATCTGCTGAAGAGACAGAGCCAATGGATCATGCACGAGCAGCCGAGGAGGCCCGGGAGAAACTGGAGATATTGAAGGTTTGACTTGCTTCTTTTCATTCATTTTGTCAGCCCTATAGAGCTGTTCAGTCACGAAAATGCAAGTAGCATCATGTTTCTGCCTCATTTTTGTAGGTGTGTTTGGAAGAGATGCCTCATCATATCAAGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8900
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 461 | 9778 | 13 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37640159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37116971 |
GRCz11 | 13 | 37242861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGTTTTATCTGCTGAAGAGACAGAGCCAATGGATCATGCACGAGCAGCC[G/T]AGGAGGCCCGGGAGAAACTGGAGATATTGAAGGTTTGWCTTGCTTCTTTT
Long Flanking Sequence:
GTTATATAATCACATTTTTATACCTGTTATGTCATATTGACAGTGATGAGAATGAAATGTACACATTTGCATTGGTTTTGTTGTACGCGATGATTTATTTTTGCATTAATGTTTATTTACATTTGTTTCAGGTTTTTCATACCTTTATTGTGTCATTTAATGAACAACGCCGGCCCGTGATGCCACTTTTAACAGCAATGAAGAGGACACCCCAACTCAGTGCTGAGCAGAAAGCTCTCAGAAGATCATGGGACACTCTCGCTGAAAAGGTCAGAGGTCAAAACAAAAATGCATGCACTTAGCATTTAGAGAACAGAAATGCATAGACATCTTATGCTAATTTGTACTGATGTGTGCATCTATGGTAGCTGCGTGAGTACAAAACAGAGCTGGACCTGACTCTCCCATCACCGCTGGACACTGTGGGCCGCTGGTTGTTGCGTATTGAAGAGGTTTTATCTGCTGAAGAGACAGAGCCAATGGATCATGCACGAGCAGCC[G/T]AGGAGGCCCGGGAGAAACTGGAGATATTGAAGGTTTGACTTGCTTCTTTTCATTCATTTTGTCAGCCCTATAGAGCTGTTCAGTCACGAAAATGCAAGTAGCATCATGTTTCTGCCTCATTTTTGTAGGTGTGTTTGGAAGAGATGCCTCATCATATCAAGAGGTTTAATACGTTTCAAAACACTAATGAGTTTGGAGAGACTCTGGTGCCGACAGACAAGATGGAAGAGATGAAGCGAAGGTATATTTGAAGGTCAAACAATCATTAGTCTAGTGTTCCCACACTTTTGGAAAGTACTGTAAAGTACCTGAATTTCAGACATGTGGATTCAAGGCCTGGAAAGTACTTAAAAACAAACACCCTAGCAAACAATTTTGTGTTTAAAAGATGTCTAATTGACATATAAATGTAGACAGCTTGGCTAAAACAAGTCTAAACTTGGGCTGTCAGTGACAATCTAATAGACATCTACGAATAGCCCAAAACTAGACTAGTTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42263
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 765 | 9778 | 19 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37635356)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37112168 |
GRCz11 | 13 | 37238058 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTGTAGAGGTGGTTTCTGGATCACTTCGTACCTACACTAAGAGACTA[C/T]AGGTACACAGTATTTGCATATACACCTAATTGCATTCATACACACATAAA
Long Flanking Sequence:
TTTTTAAATAAGTAGTTTGAACAAGCCGGAAACATCATTTTTTGGAGTGTAGCTAGGCAAAGCTTACATATTTTAATAGCTGCTTGTGTGTTCACTGGATTGTAAACCTGATGATTTTCTTAGGTGACCTCATCAGTGATGTCAGAATGGAGTTCTCGCCAAGCTCACCTGAACGATGTGGCCAGCTACCTGATAGAGGTCACAGACCCGCAGACTAGCCGCGCTATTTCAGATGAACTCTGCAGGATCAACCTCCTCTGGGCTGACTTTGCTAAAACATCTCAGTTTGTGAGTCACCTATCATGTTCAAACTTGAATATAGATGAACTCAGATGATTTAATGCATCTTGCATATTGCATTTCAGTATTTAGCTGAGGAGCCCCGTGCTGCCCCTTCCAGCCCTCAGACAGTTCAAGCACTGATGAGAGAGGCCACTCAGTTACTGAAAGAACCTGTAGAGGTGGTTTCTGGATCACTTCGTACCTACACTAAGAGACTA[C/T]AGGTACACAGTATTTGCATATACACCTAATTGCATTCATACACACATAAAAATAGACAATATATATTTCATGTCTTGATAATATGCCTATTCACCTTATTCTTTGCCGACGAGCAGGCGCAGCCATTTGAATCTTTTTGGCACGAGACTTCCGGTCTTATTCACTTCAATTCATTTTTAGAGTTTAAAAACTGCTCATTACGCTGCTTGATGTTGCAAACTGATATTTTCTTATTATATGATTCTACTTGGTCTGTATAGTAATGCAAACATTTGTTTGTAGAGCAAGTAGTTTGACCGTTTTCTACCGTTTATTATTCCTTGTCATTTCTCCCATAGATGACTAAATCAGAAGTTTTAAAACAATCACAAAAACAGGAGCACTTCCGCATTTTAGAATAAGGTCAATACAGAATGTACGGCCACAACATTTTTTTTTTTAAATTTAATTAATTTTATTGATTAACATGCAAATGTTTAGATGTTTTATGTACAATACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31954
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 1010 | 9778 | 23 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37632201)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37109013 |
GRCz11 | 13 | 37234903 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTATGATTGTTGTACAAGACTATGAAGCGGAGAAAGGTAGCCCACAAT[C/A]ACAAATACACCCCTGTGAGCAGGAAAAAGACTGTCAGTCCATTGAGCTTA
Long Flanking Sequence:
GCTGCTGTTGAAAAGTCACAGGTCTGTCAATTATTTATAGATGAAAATGGTTGCATCAAATAAAGAAAATGTACAACGCTGAAACTACCAAAAACTAATCACTAAGTAATTAGCAATCAGGATGTATTATCTAAGCATAACTAACCTTGTTTTAGAATTGTGTGCAAATGCATTATAATTTTTAAATTATGTTAAATTTTACCAGGAAGCTGTAGGGATGCTCAGCTCTTTGGGGTCTTGCAGAGACAGAAGCCCTTCCAGAGACCAGCCCCCTTCAAAGATATTTGTCCTGTATCAAGAGGCCGAGAAAGAGTCCCAAACCTCTCAATCGGGAGCCACTAGCCAACCAGAAACCCAGCCCACAGTTAGGGCAAAAGTCCCAATATCTTCTCAGATGCCCTCAGAGGTACCTTCTGTAGTCCTCAAGACCCAGCAGTGTAGTCAGCCTGTACCTATGATTGTTGTACAAGACTATGAAGCGGAGAAAGGTAGCCCACAAT[C/A]ACAAATACACCCCTGTGAGCAGGAAAAAGACTGTCAGTCCATTGAGCTTAAGTCACAAAAAGTTGTCGAAGCTCAAGCAAAAAGTCACATAGTCAAAGAACATTGTGTAGAAAGTCAGACAACACAACAGCTGGCAGAAAACCAGAGACAGGTGCAAGCTCCAATACCCAGCCAACCTTCACAAAATCAACAAAAAGTAGCATCTCAAGGTCATCATGAACAACAACTAACAACACAGGCACATGTGCAGATCCAACAACAAGATAAAACTCAATCTTCAAAACAGCAAATGGTTCAAGGATTAATGTCAACACAGCCACAACTTCAGGACCAATTAGAAGCACAACCACAGAAAGACATTACAGGTCAAAATCAAGCTCCAAAGCAGAAGAGGAAATCTAAAAAGTCCCAGGCAAATCTGCAGAACAGGCCTTGGCTACAACAGAGGAGTCAATTGGAAAACGTTACCCCCAAAACAGCTCAAGAGGTCCCACAGTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42262
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 1021 | 9778 | 23 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37632167)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37108979 |
GRCz11 | 13 | 37234869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGTAGCCCACAATCACAAATACACCCCTGTGAGCAGGAAAAAGACTG[T/A]CAGTCCATTGAGCTTAAGTCACAAAAAGTTGTCGAAGCTCAAGCAAAAAG
Long Flanking Sequence:
TTATAGATGAAAATGGTTGCATCAAATAAAGAAAATGTACAACGCTGAAACTACCAAAAACTAATCACTAAGTAATTAGCAATCAGGATGTATTATCTAAGCATAACTAACCTTGTTTTAGAATTGTGTGCAAATGCATTATAATTTTTAAATTATGTTAAATTTTACCAGGAAGCTGTAGGGATGCTCAGCTCTTTGGGGTCTTGCAGAGACAGAAGCCCTTCCAGAGACCAGCCCCCTTCAAAGATATTTGTCCTGTATCAAGAGGCCGAGAAAGAGTCCCAAACCTCTCAATCGGGAGCCACTAGCCAACCAGAAACCCAGCCCACAGTTAGGGCAAAAGTCCCAATATCTTCTCAGATGCCCTCAGAGGTACCTTCTGTAGTCCTCAAGACCCAGCAGTGTAGTCAGCCTGTACCTATGATTGTTGTACAAGACTATGAAGCGGAGAAAGGTAGCCCACAATCACAAATACACCCCTGTGAGCAGGAAAAAGACTG[T/A]CAGTCCATTGAGCTTAAGTCACAAAAAGTTGTCGAAGCTCAAGCAAAAAGTCACATAGTCAAAGAACATTGTGTAGAAAGTCAGACAACACAACAGCTGGCAGAAAACCAGAGACAGGTGCAAGCTCCAATACCCAGCCAACCTTCACAAAATCAACAAAAAGTAGCATCTCAAGGTCATCATGAACAACAACTAACAACACAGGCACATGTGCAGATCCAACAACAAGATAAAACTCAATCTTCAAAACAGCAAATGGTTCAAGGATTAATGTCAACACAGCCACAACTTCAGGACCAATTAGAAGCACAACCACAGAAAGACATTACAGGTCAAAATCAAGCTCCAAAGCAGAAGAGGAAATCTAAAAAGTCCCAGGCAAATCTGCAGAACAGGCCTTGGCTACAACAGAGGAGTCAATTGGAAAACGTTACCCCCAAAACAGCTCAAGAGGTCCCACAGTCTCAGCCAAAACCAGTGTACAAAGGCCAAATAAGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22357
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 1362 | 9778 | 23 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37631146)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37107958 |
GRCz11 | 13 | 37233848 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAACCACAAAGATTTACAGTGGCCCAAGCAATGCCCCAAGGTATTTCC[A/T]GACCAGTCCAGCAGTACCCAACACCTCCCATGCAACCACAAATGATTATG
Long Flanking Sequence:
TAGTTGCTGTTAGCCCTACAGAAGCTCAGGGACCTCCTCAAAGCAGTGTGACAGCACAGCCAAAATATGTTGTTGAGAGTGATGAGAAGTGCCTGAAGCAAAATCAACCTGTTGCACAGGAGAAGGTGACACAAAGACTAGCTCAAACTGAGCCAGTAGTACCCGCACAACCAATGACACAAAAACAACCACAACAGTCAATGACTGTTACAAATCATCAAGTTCTAAGCCAACCTCAACCTGCTATATTAACTCAAGCCCAAGCAGCTTTAAAAACCGCACATGCTGCACCTATTCAACAACAAAAACAACCTCACATGGTGAAATCACAGCAACCTGATGTGATGATCCCAAAACAAGCACAACCTCAATTCATGACTCCCATGCAGCCACAAGTTATGCCCCAATGGCAGCCTCAACAGACCATCCTTCAGTCTCACCCTGCAGTACCACAACCACAAAGATTTACAGTGGCCCAAGCAATGCCCCAAGGTATTTCC[A/T]GACCAGTCCAGCAGTACCCAACACCTCCCATGCAACCACAAATGATTATGCCGAGGCAACAGTCACCACATGGAGCAGTGCAAACTCAGTCACAAATACTCCACAGTCCGACGGTACTTGCCCCTCAATCCAAAGGTGCATCCCCCATACAACCCAGAATCATCTCTATGCCTCAGTCTCAGATGCCTGTTCAAACTCAGACCCAACCTCAGCTGAAAGCACAGGGAAGTGCTCCACTTATGACTCAACCTGAAGGGCAACCACTGTGGTGTCCACCCCGAGATGCCACCCAAAATTACCCCAAAATTCAAGGACCAGTTTCTGCCCAAATGCAGCCTCTGGCTCATTTCCAAACTCATCCCCAACCTCAAAGCTTCCCTCCAGCCCAACCTCAGCAATGGTCACCAACAAGACCAGGCATTGTAGCCCAGACCTATCCCACTGTTCCAGGTCAGGCAGTACAACCCCAACCTCAATTATCTGTTTATCCTAAAACCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16388
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 1452 | 9778 | 23 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37630874)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37107686 |
GRCz11 | 13 | 37233576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGGAAGTGCTCCACTTATGACTCAACCTGAAGGGCAACCACTGYGGTG[T/A]CCACCCMGAGATGCCACCCAAAATTAYCCYAAAATTCAAGGACCAGTTTC
Long Flanking Sequence:
AAAACCGCACATGCTGCACCTATTCAACAACAAAAACAACCTCACATGGTGAAATCACAGCAACCTGATGTGATGATCCCAAAACAAGCACAACCTCAATTCATGACTCCCATGCAGCCACAAGTTATGCCCCAATGGCAGCCTCAACAGACCATCCTTCAGTCTCACCCTGCAGTACCACAACCACAAAGATTTACAGTGGCCCAAGCAATGCCCCAAGGTATTTCCAGACCAGTCCAGCAGTACCCAACACCTCCCATGCAACCACAAATGATTATGCCGAGGCAACAGTCACCACATGGAGCAGTGCAAACTCAGTCACAAATACTCCACAGTCCGACGGTACTTGCCCCTCAATCCAAAGGTGCATCCCCCATACAACCCAGAATCATCTCTATGCCTCAGTCTCAGATGCCTGTTCAAACTCAGACCCAACCTCAGCTGAAAGCACAGGGAAGTGCTCCACTTATGACTCAACCTGAAGGGCAACCACTGTGGTG[T/A]CCACCCCGAGATGCCACCCAAAATTACCCCAAAATTCAAGGACCAGTTTCTGCCCAAATGCAGCCTCTGGCTCATTTCCAAACTCATCCCCAACCTCAAAGCTTCCCTCCAGCCCAACCTCAGCAATGGTCACCAACAAGACCAGGCATTGTAGCCCAGACCTATCCCACTGTTCCAGGTCAGGCAGTACAACCCCAACCTCAATTATCTGTTTATCCTAAAACCCAGCCACAACCACAGCCTCAGCAATGGCTCTCTCCAAGACCTGAATCACCTTGGGGTCAATCACAGATAAGACCTCAAGGTCCAGTTCAGCCTTGGAGGCCAGTCAGTCCAGAGAGTGTCAGCCCAGTATACCCCAGGGCTGAAACTCAAGGGCAAGGACTACATCCTCAGTCCCAATATCAACCCCTACCAAGGCCACAAAGCCCTCAACGGCAGTGGGGTCCAGTCAGGACAGAACATCAGTTTCAAGTTTCTTCCCAGACTACATTACATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42261
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 1524 | 9778 | 23 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37630658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37107470 |
GRCz11 | 13 | 37233360 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCACTGTTCCAGGTCAGGCAGTACAACCCCAACCTCAATTATCTGTTTA[T/A]CCTAAAACCCAGCCACAACCACAGCCTCAGCAATGGCTCTCTCCAAGACC
Long Flanking Sequence:
CAAGGTATTTCCAGACCAGTCCAGCAGTACCCAACACCTCCCATGCAACCACAAATGATTATGCCGAGGCAACAGTCACCACATGGAGCAGTGCAAACTCAGTCACAAATACTCCACAGTCCGACGGTACTTGCCCCTCAATCCAAAGGTGCATCCCCCATACAACCCAGAATCATCTCTATGCCTCAGTCTCAGATGCCTGTTCAAACTCAGACCCAACCTCAGCTGAAAGCACAGGGAAGTGCTCCACTTATGACTCAACCTGAAGGGCAACCACTGTGGTGTCCACCCCGAGATGCCACCCAAAATTACCCCAAAATTCAAGGACCAGTTTCTGCCCAAATGCAGCCTCTGGCTCATTTCCAAACTCATCCCCAACCTCAAAGCTTCCCTCCAGCCCAACCTCAGCAATGGTCACCAACAAGACCAGGCATTGTAGCCCAGACCTATCCCACTGTTCCAGGTCAGGCAGTACAACCCCAACCTCAATTATCTGTTTA[T/A]CCTAAAACCCAGCCACAACCACAGCCTCAGCAATGGCTCTCTCCAAGACCTGAATCACCTTGGGGTCAATCACAGATAAGACCTCAAGGTCCAGTTCAGCCTTGGAGGCCAGTCAGTCCAGAGAGTGTCAGCCCAGTATACCCCAGGGCTGAAACTCAAGGGCAAGGACTACATCCTCAGTCCCAATATCAACCCCTACCAAGGCCACAAAGCCCTCAACGGCAGTGGGGTCCAGTCAGGACAGAACATCAGTTTCAAGTTTCTTCCCAGACTACATTACATGGAGTTCCCCATCCAATTGCTCCATGGAATCAGCCAACTGTTAAAGCTCCCATAAGACCTCAGAGTCCACAACAGCCCCAGCAAAGCCAGCAACAGTGGGGTCCATCCAGGACAGACGCCCCATCTGAATCCCTCATCCAAAGCCAAGCTTTCCAGGGAGAATTTCAGCCCCAAGATCTGACAAAGCCACAATTGCCAGTACAGGAACCACCCCAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28172
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 1877 | 9778 | 26 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37626985)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37103797 |
GRCz11 | 13 | 37229687 |
KASP Assay ID:
2260-6787.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCTTTTTATTAACCAATAGTTCACAAACTGAGCAAGCAAAAGAGCCA[C/T]AAACTCAGAAAGCACCGACAATCCCACCACCTGTTGAGAAGCCCAAAGAG
Long Flanking Sequence:
TCATTTAACAGACTCTTTTATTGAAAGTGACTTACAAACGAGGATAAACGAAGCACTTTAATCAACAGAGAGTAGCATTATATAAATGCTATGACAAGTAATTAAAATGAGGAGAAAGTGTCACTTACAGGTGGTTTGTAAACGCTTGAGAAATCCCAAATGTTTTCAAAAAGCATGGAGTGTTGATAAATAGTCTGATGTAAATGGACAGAGTGTGTCTCGCAAGTCACAAAAGATGACAATTTAAAGAAAGCTAGAAACCTGGAACCGCTGACTTCCATGGTATTTGCTCTTCCTACTATGGACGGCAATGGTTACAGTTTTTTAGCTTTCATCAAAATATATTGTTTCAAGATCAATAGAATAAAGAAACTCATAATGGCTTTGAACCACTTAATGATGAGTTAATAGTTAGTGCGTTCTCCTTTTTCGGTAAACTAACCTTTAAATGTTTCTTTTTATTAACCAATAGTTCACAAACTGAGCAAGCAAAAGAGCCA[C/T]AAACTCAGAAAGCACCGACAATCCCACCACCTGTTGAGAAGCCCAAAGAGGTTAATATCCCTGAGGTAAAACTTTATGAATATTTTATATCACCTGTATATTATGTATTTTAGAACCTATTAAATTTACAAACAGAAAAGTTACCTTTTGTTATTGTATCTACTGTAGATAAGCATGCAGTGAACTGACTGTTTTACTAGGACTGAATGAAAGATGTTGAGCACTTGTGATGTTGTTTTAGGGTGTTATACCAGTTAGCCCCCAGCGACCGAGAACTGTGGAGAAGAGAGAGATAGTGAAACAAACGAGTACAGAAGAGGACAGGTATGGATTTAAAAAGAAAACAGCTTTATATGTTACTATATTCAGTACGATTTAATTTTGTGTGTGGATCTTATGGTCTACCTCTTTTTTCCTTGCACCACTCAGGTACCGTAGCTCCAGATTCGCATTACAGGGTCAGCTAAATAGAAATGAACAATGCATGCTGGGAGATCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11835
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 1926 | 9778 | 27 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37626660)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37103472 |
GRCz11 | 13 | 37229362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGYGGAGAAGAGAGAGATAGTGAAACAAACGAGTACAGAAGAGGACAG[G/A]TATGGATTTAAAAAGAAAWCAGCTTTATATGTTACTATATTCAGTACGAT
Long Flanking Sequence:
TAGCTTTCATCAAAATATATTGTTTCAAGATCAATAGAATAAAGAAACTCATAATGGCTTTGAACCACTTAATGATGAGTTAATAGTTAGTGCGTTCTCCTTTTTCGGTAAACTAACCTTTAAATGTTTCTTTTTATTAACCAATAGTTCACAAACTGAGCAAGCAAAAGAGCCACAAACTCAGAAAGCACCGACAATCCCACCACCTGTTGAGAAGCCCAAAGAGGTTAATATCCCTGAGGTAAAACTTTATGAATATTTTATATCACCTGTATATTATGTATTTTAGAACCTATTAAATTTACAAACAGAAAAGTTACCTTTTGTTATTGTATCTACTGTAGATAAGCATGCAGTGAACTGACTGTTTTACTAGGACTGAATGAAAGATGTTGAGCACTTGTGATGTTGTTTTAGGGTGTTATACCAGTTAGCCCCCAGCGACCGAGAACTGTGGAGAAGAGAGAGATAGTGAAACAAACGAGTACAGAAGAGGACAG[G/A]TATGGATTTAAAAAGAAAACAGCTTTATATGTTACTATATTCAGTACGATTTAATTTTGTGTGTGGATCTTATGGTCTACCTCTTTTTTCCTTGCACCACTCAGGTACCGTAGCTCCAGATTCGCATTACAGGGTCAGCTAAATAGAAATGAACAATGCATGCTGGGAGATCATCCCTCAGAATCAGTCACTCCTACAGACCTGCAGAAACGACTGAGAGAATTAAAGGTAATAGTTTTAAGTTAGTCATTTCAGAATAATACTTTAGAATAATGGTCCATTAGTGAATGTTAGTTACTTTATTTACTAACATTTAGTATGAACAATCTTACTAACAGTAACTAATGCATCATTAAATTCCAATGTTATGCTTGTTAACATTAATTAATGCACTCCGAGTTAACATGAACTAACGTTATTTAACTTAAATATCATGATGAATACAGATATTCAGAATTAACAGAGAATACAGATGAATAAATCCCATAATAAACAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13694
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 1926 | 9778 | 27 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37626660)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37103472 |
GRCz11 | 13 | 37229362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGYGGAGAAGAGAGAGATAGTGAAACAAACGAGTACAGAAGAGGACAG[G/A]TATGGATTTAAAAAGAAAWCAGCTTTATATGTTACTATATTCAGTACGAT
Long Flanking Sequence:
TAGCTTTCATCAAAATATATTGTTTCAAGATCAATAGAATAAAGAAACTCATAATGGCTTTGAACCACTTAATGATGAGTTAATAGTTAGTGCGTTCTCCTTTTTCGGTAAACTAACCTTTAAATGTTTCTTTTTATTAACCAATAGTTCACAAACTGAGCAAGCAAAAGAGCCACAAACTCAGAAAGCACCGACAATCCCACCACCTGTTGAGAAGCCCAAAGAGGTTAATATCCCTGAGGTAAAACTTTATGAATATTTTATATCACCTGTATATTATGTATTTTAGAACCTATTAAATTTACAAACAGAAAAGTTACCTTTTGTTATTGTATCTACTGTAGATAAGCATGCAGTGAACTGACTGTTTTACTAGGACTGAATGAAAGATGTTGAGCACTTGTGATGTTGTTTTAGGGTGTTATACCAGTTAGCCCCCAGCGACCGAGAACTGTGGAGAAGAGAGAGATAGTGAAACAAACGAGTACAGAAGAGGACAG[G/A]TATGGATTTAAAAAGAAAACAGCTTTATATGTTACTATATTCAGTACGATTTAATTTTGTGTGTGGATCTTATGGTCTACCTCTTTTTTCCTTGCACCACTCAGGTACCGTAGCTCCAGATTCGCATTACAGGGTCAGCTAAATAGAAATGAACAATGCATGCTGGGAGATCATCCCTCAGAATCAGTCACTCCTACAGACCTGCAGAAACGACTGAGAGAATTAAAGGTAATAGTTTTAAGTTAGTCATTTCAGAATAATACTTTAGAATAATGGTCCATTAGTGAATGTTAGTTACTTTATTTACTAACATTTAGTATGAACAATCTTACTAACAGTAACTAATGCATCATTAAATTCCAATGTTATGCTTGTTAACATTAATTAATGCACTCCGAGTTAACATGAACTAACGTTATTTAACTTAAATATCATGATGAATACAGATATTCAGAATTAACAGAGAATACAGATGAATAAATCCCATAATAAACAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42260
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 1967 | 9778 | None | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 37626430)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37103242 |
GRCz11 | 13 | 37229132 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAATCAGTCACTCCTACAGACCTGCAGAAACGACTGAGAGAATTAAAGG[T/A]AATAGTTTTAAGTTAGTCATTTCAGAATAATACTTTAGAATAATGGTCCA
Long Flanking Sequence:
ATATCCCTGAGGTAAAACTTTATGAATATTTTATATCACCTGTATATTATGTATTTTAGAACCTATTAAATTTACAAACAGAAAAGTTACCTTTTGTTATTGTATCTACTGTAGATAAGCATGCAGTGAACTGACTGTTTTACTAGGACTGAATGAAAGATGTTGAGCACTTGTGATGTTGTTTTAGGGTGTTATACCAGTTAGCCCCCAGCGACCGAGAACTGTGGAGAAGAGAGAGATAGTGAAACAAACGAGTACAGAAGAGGACAGGTATGGATTTAAAAAGAAAACAGCTTTATATGTTACTATATTCAGTACGATTTAATTTTGTGTGTGGATCTTATGGTCTACCTCTTTTTTCCTTGCACCACTCAGGTACCGTAGCTCCAGATTCGCATTACAGGGTCAGCTAAATAGAAATGAACAATGCATGCTGGGAGATCATCCCTCAGAATCAGTCACTCCTACAGACCTGCAGAAACGACTGAGAGAATTAAAGG[T/A]AATAGTTTTAAGTTAGTCATTTCAGAATAATACTTTAGAATAATGGTCCATTAGTGAATGTTAGTTACTTTATTTACTAACATTTAGTATGAACAATCTTACTAACAGTAACTAATGCATCATTAAATTCCAATGTTATGCTTGTTAACATTAATTAATGCACTCCGAGTTAACATGAACTAACGTTATTTAACTTAAATATCATGATGAATACAGATATTCAGAATTAACAGAGAATACAGATGAATAAATCCCATAATAAACAACATAGGCTAATTCTGAAAACATAGCCCTATGAACGTTCCTAGAGATCGCAAATTATGTAGCCAGAGGTACGTATGGCAGCATTTCGTCTTTAAAAGGAATGCTACAGGCGATGTGATGCTGTTCCTTTCGGGATTACTAGCTGACCGCTTACCTCCATGAGGATGGCTTTACCGCTATTACCAGTGAATTTGTCCAGTTGTGTGCTGTGTACGTCGGAGGGTTTCAGATGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31953
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 2329 | 9778 | 33 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37619322)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37096134 |
GRCz11 | 13 | 37222024 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCATGTTTTTGTGTATTTCACAGATTAGAACAATGCACTGTTCTCATG[G/T]AACTGCTGAAGAAGTTTCAGAACTGCCGCACTTACCTGACCAACACACTC
Long Flanking Sequence:
TTTTGATCTTTGAAATGCAACTAAATTCAAATTATAAACGAAACCTGAGAGAAGGAAACCAATGAAAATTTATACGAAAAAACTTTGCTATTTAAAAATAGTTGTAAAAAGAAAAGTCACTATAGGTTAAATGATGGATATATGCTGAACACATTTTATAATTTTTTTTATTCATCCATAAACATTGATTAAAGCACATACGTAACGTACATAGATCATATTAAATATGGTACAATAAAAAGCACCAAAAGGTGAAAAACTTCAAACGTTTTATTGTAATGAACCTTCAGTGGATAAAAACTTTATTGAAAATTATATCAATTCATGTTTTGAAGATATGTGAAGGTTTTAAGTGTCTGTGTTGTCATTTTTGGGTGCACTAACTGGTTCTTCGTTTGTACAAAGGAACTTACTGTGATGGGCAGAACCTCAGAGTTTGTAAACTGATATGTGCATGTTTTTGTGTATTTCACAGATTAGAACAATGCACTGTTCTCATG[G/T]AACTGCTGAAGAAGTTTCAGAACTGCCGCACTTACCTGACCAACACACTCCAGAGGGCAGAGCAAACAAGCAGCGAGCAGGCATCATACATGGGCAAAGACAACCTGCAACGCCTCCTAGCTAAAGTATGCCAACACTAATCACAAATAAATGCTAATGTATTCATTTCTTATGGGGACACACCATCAAGTATCTTTCACAGAAGTTTTTTTTTTCACCACCAGGGGTCAGTCAGTGCTCACTTTTTGAACTCAGAATTGTTGATGGTTTTATTTTTAAAGTTCATACTATAATTAAACTTTTCATTAGCACTAAACTTGAGTTTTCAACATCTACATGTATAGACAGATCTTTTATTAGTCTGAACAAGGTTTCTTTCTCCATTGTTCTGACTAAACAGCTGCATTCATTTCTGTAGTGCTTTTTAGATGCTTGTTATCATCTGCAATACCCACATAGACATCTGACACAGAAATATGCAAATAAATATATATTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16245
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 2783 | 9778 | 41 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37611451)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37088263 |
GRCz11 | 13 | 37214153 |
KASP Assay ID:
2260-6784.1 (used for ordering genotyping assays)
KASP Sequence:
AGGACTGGCTTCAGCAGAGGGAACAAGTGCCAGAACAGAGAGAAAAACTA[C/T]GACAAATCCAAGAGGAGTTTCTTAAAGAAAGGTAACACTTGCTTTTCTAA
Long Flanking Sequence:
AAGCTTTGTTCTCCACGTGGCATCAGGAACAGGAAGGAGAACTGGCCACACTGAGAGCACACTGTCAGGGACGCCATAAACAGCTAGATGACATCCTCTACAACCTCAACAGGTACACAGACTGAGCTCTTGTCATAGATTTTTGCTGTTGCTGTTGATTGAGCCAATTATTTAAATTAATGTTTTTAATCCAATTCGTCTTTTTTTCTATAGCGCTTTTACAATGTAGATTGTGTCAAAGCTGCTTAACATAGAAAGAGAAGAGAGAATAAAAAGCCATAACAATATTTTAGATGGGAACATTCCAGGCAGACTGGGGAGTAGTGGTGGAATGCTGGTGTAGTTCTAGTTAGATTAAACTGTTTTAGTTCAATTTAATGACACTATTGAAGTTCAGTTCAGTTGTGTGTCTTTATGTGTTTAGCTTGCAAGAGGAACACAATCATTTAAAGGACTGGCTTCAGCAGAGGGAACAAGTGCCAGAACAGAGAGAAAAACTA[C/T]GACAAATCCAAGAGGAGTTTCTTAAAGAAAGGTAACACTTGCTTTTCTAAATGTAAAGTTTGTTTTAAACATTTTTTGTTTTTTCAAACAATAATTTCAGTAATTAAATAACACATTCACAGCATATTTACTTGGTATTCCTAATTATAATTTTATACATAATAATAATAAGAGCAATACGATACTATTATTATATATACACTCACTGGCCACTTTATTAGGTACACCTTACTAGTTAGACCTACTTTTGCCTTCAGAACTGCCTTAATTCTTTATGGCATAGATTCAACAAGGTACTGGAAATATTAATCAGCAAATTTGCTCCATATTCACATGATAGCATCACGCAGTTGCTGCACATCCATGATGCAAATCTCCCTTTCCACCACATCCCAGAGGTGTTCTATTGGTTTGAGATCTGGTGACTGTGGAGGCCATTTGACTACAGTGAACTCATTATCATGTTCAAGAAACCAGTCTGAGATAATTCGTGCTTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35561
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 2857 | 9778 | 42 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37609577)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37086389 |
GRCz11 | 13 | 37212279 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCACAAGACCCTTGATGCCCAGATTGAAACATTCCAAACTAATGCAGAA[C/T]AGATCAGAGCCTGGATCAGAGATTTAAAGCAAGGACTCGAACACTTGAGC
Long Flanking Sequence:
TATTAGTCTCTGATTTTATTTAATTTGAGATTTATATGGTAAAATTATGAAAAATGTTTGAAAAGAAAATGATCCTGCCACAAAATGTTTGAATTTATGTATGTGGACAACATTTATGGCCAACCAAAGCTTAAAGAAGATGAAACCATAAGATCTCGAGCCACTCATGTAAATGAACACAATGTCACACTTTATTGGACTGAAATACATTTTGATACTTTGCATGATTTCAGTTTATGTTGTGCAATTGTTCAGCCTTTTTTATTTCACATAAACCTGTATAACACTTACTTTCACCCTCAATCCACAGCGGTCGTGTAGAGGCATTCAATGACCTGTTATCCACAGTAAGGATGCGTGGCCTGAGAGGAGACCCTTTCCTTAAAGACAGCGAGACCCTAATTGACCAATACCACAGCCTGGGGGTTATTTTAGAAAATCAAGCCCAAGACCACAAGACCCTTGATGCCCAGATTGAAACATTCCAAACTAATGCAGAA[C/T]AGATCAGAGCCTGGATCAGAGATTTAAAGCAAGGACTCGAACACTTGAGCACTGACACACCAATGCAAGAAAAAGATATGAAGGCTCAGGTGGGTTCCCATACATTGTCATACTTCGAAATAATCCAAAAAAGATATAAATAGTGATTACTTAATTTTTTAAAACTTGTATATATTTATTTTTTGCTTGATTTTCTGGTAAACACAAAGAATATCTTTACAAACATCCTTAATGTATTTAGGATAATATGAATGTTTATCTGTTTTTTTGTTTTAAGGCTGTTCTTAATCAAAGCTCTGATGGTGACGCTAAACTGGTGGCTCTGAAAGGTGAGGGTGTTGCTTTATGTACACATGAGATTTTGGAGGAGACCAGAAGACAAGAACTTGTTCACACACTTAAAAACATCGAGGATGAATGGAAAAGAGTTCTGGATTTGGCCCAACTCCTAAAACATCAGGCAGAACTCCAAGACACTCTTCACAGGGAACTAGAAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35560
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 2931 | 9778 | 43 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37609167)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37085979 |
GRCz11 | 13 | 37211869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGGAGGAGACCAGAAGACAAGAACTTGTTCACACACTTAAAAACATC[G/T]AGGATGAATGGAAAAGAGTTCTGGATTTGGCCCAACTCCTAAAACATCAG
Long Flanking Sequence:
TACCACAGCCTGGGGGTTATTTTAGAAAATCAAGCCCAAGACCACAAGACCCTTGATGCCCAGATTGAAACATTCCAAACTAATGCAGAACAGATCAGAGCCTGGATCAGAGATTTAAAGCAAGGACTCGAACACTTGAGCACTGACACACCAATGCAAGAAAAAGATATGAAGGCTCAGGTGGGTTCCCATACATTGTCATACTTCGAAATAATCCAAAAAAGATATAAATAGTGATTACTTAATTTTTTAAAACTTGTATATATTTATTTTTTGCTTGATTTTCTGGTAAACACAAAGAATATCTTTACAAACATCCTTAATGTATTTAGGATAATATGAATGTTTATCTGTTTTTTTGTTTTAAGGCTGTTCTTAATCAAAGCTCTGATGGTGACGCTAAACTGGTGGCTCTGAAAGGTGAGGGTGTTGCTTTATGTACACATGAGATTTTGGAGGAGACCAGAAGACAAGAACTTGTTCACACACTTAAAAACATC[G/T]AGGATGAATGGAAAAGAGTTCTGGATTTGGCCCAACTCCTAAAACATCAGGCAGAACTCCAAGACACTCTTCACAGGGAACTAGAAAATCTACAGGCCCAAGAAGAGAGTACCCAATCCTGGGTGAGAGAGCAGCTGCAGATGCTACGCTCCTTGGAGAAGGAACTTCAACCCCAGGAAAAACTCAACAAATTACTGGTAAGCACAAAGAAAAATTATATTTTGACTGCAAAACCCTTTTTAGAACTCTCTAGTAATTCTTACCTTGGTTGATTGGTTTATAACATGTATATATTCTCTAGGCTGTCTTAGACCTTGCTGATGAAGCTGATTCCAGATTGGCCAGTTTACAGAGGCAAGGACAGAGTTTATGTTCTTATAAAGAGCTTGACACTGAGAGGAGGAGTCACATTGACCAAACCCATAGAGCAATAGAGGAGGAGTGGAGGAAAGTGCTGCAACTTGCTCAGGAGCTTAAGAACCAGGTCAAGCATGAGGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22356
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 3017 | 9778 | 44 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37608805)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37085617 |
GRCz11 | 13 | 37211507 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTTGCTGATGAAGCTGATTCCAGATTGGCCAGTTTACAGAGGCAAGGA[C/T]AGAGTTTATGTTCTTATAAAGAGCTTGACACTGAGAGGAGGAGTCACATT
Long Flanking Sequence:
TTTAAGGCTGTTCTTAATCAAAGCTCTGATGGTGACGCTAAACTGGTGGCTCTGAAAGGTGAGGGTGTTGCTTTATGTACACATGAGATTTTGGAGGAGACCAGAAGACAAGAACTTGTTCACACACTTAAAAACATCGAGGATGAATGGAAAAGAGTTCTGGATTTGGCCCAACTCCTAAAACATCAGGCAGAACTCCAAGACACTCTTCACAGGGAACTAGAAAATCTACAGGCCCAAGAAGAGAGTACCCAATCCTGGGTGAGAGAGCAGCTGCAGATGCTACGCTCCTTGGAGAAGGAACTTCAACCCCAGGAAAAACTCAACAAATTACTGGTAAGCACAAAGAAAAATTATATTTTGACTGCAAAACCCTTTTTAGAACTCTCTAGTAATTCTTACCTTGGTTGATTGGTTTATAACATGTATATATTCTCTAGGCTGTCTTAGACCTTGCTGATGAAGCTGATTCCAGATTGGCCAGTTTACAGAGGCAAGGA[C/T]AGAGTTTATGTTCTTATAAAGAGCTTGACACTGAGAGGAGGAGTCACATTGACCAAACCCATAGAGCAATAGAGGAGGAGTGGAGGAAAGTGCTGCAACTTGCTCAGGAGCTTAAGAACCAGGTCAAGCATGAGGAATCTCTCAACAGAGAGTTACAAAGCTTTTGTGATCAGGGAGAAGAGACTCAATCCTGGGTTAGACAGCTCAGAGAGACCTTGGAGACCCTTCATATGACATCTTCTATTCAAGAGAAGCTCAGTGGTGTTGAGGTAATGGAGAGTATTTTAGGGCAATTTATTGCTTGTTAAAGAAACAAGGCAATGTTTCCTGAAACAGTAAATATACACTGAAAACCAGTAAAAAATGTAAACAAAAGCATGATATCTTGGTTTTGTGTTTTTTTTAGGCAGTACTTGCTCATAGATCTGAGGGGGACTATAAACTTAGTGACCTAAAGATGAAGGGAGAGAGTCTATGTTCCTATGAAGATCTACAGGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42259
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 3216 | 9778 | 45 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37608068)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37084880 |
GRCz11 | 13 | 37210770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTGCTAGGTGAAGATACTCAAATTCAGGAGAAAATGAATGGAGCTCAG[G/A]TATAGTAAGAGCCAAAGAGTGATATTCTAGTTCACTTACCAAATATCCAC
Long Flanking Sequence:
TCTTCTATTCAAGAGAAGCTCAGTGGTGTTGAGGTAATGGAGAGTATTTTAGGGCAATTTATTGCTTGTTAAAGAAACAAGGCAATGTTTCCTGAAACAGTAAATATACACTGAAAACCAGTAAAAAATGTAAACAAAAGCATGATATCTTGGTTTTGTGTTTTTTTTAGGCAGTACTTGCTCATAGATCTGAGGGGGACTATAAACTTAGTGACCTAAAGATGAAGGGAGAGAGTCTATGTTCCTATGAAGATCTACAGGAGGGTAAACGCCAGACAATCCAACAGACATTACAAGAAGTAATGCAAGAGTGGACAGAAGTTTTGTTAAATGCTCAGGAGTTGAAGAACCAATCAGAACTTGAGGAGTCTCTTTGTAAGGACCTTCTGGATCTTCAAGAACAGGAGGAGAGCATTCAATCTTGGATCAATGAGCAGCATCTTAAGATCAAATTGCTAGGTGAAGATACTCAAATTCAGGAGAAAATGAATGGAGCTCAG[G/A]TATAGTAAGAGCCAAAGAGTGATATTCTAGTTCACTTACCAAATATCCACAAACATTCTGACTTACTCGCTGGCCTAAAATGTTTGTTTACTCTAGGGCATCCTGAACTCAGAATCAGAAGGAGATTATAAAATAGCCACCCTGAGAAGAAAAGTGGACGGTTTGTGCTCTCGAGAAAACCTGAGCGAGGACAGAAAACAGGAAGTCCAGCTAAACTTGAGGTCAGTTGAAGAGGAATGGAAGAAGGTCTTGGCTGGTGCTCAGCAACTAAAGAACCAGGCTGAGCTCCAGGATTCTCTTGCAAGGGAGCTTCAGACTTTTTATGCCCAGGAGGAGAGCACCTGGTCCTGGGTGAGGAACCAGAAGGATGTCCTGTACTCACTGGGGGAAAACACTCATGGTACACAAGACCAGCTTGAAGAGAGACTAAGCAGAGCACAAGTAAGTATTAATATAGGCTCAGCAGTGGAAGTCATCACAGTTGGGTAAACTTGGAGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2693
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 3331 | 9778 | 46 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 37607625)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37084437 |
GRCz11 | 13 | 37210327 |
KASP Assay ID:
554-2892.1 (used for ordering genotyping assays)
KASP Sequence:
CACTCATGGTACACAAGACCAGCTTGAAGAGAGACTAAGCAGAGCACAAG[T/G]AAGTATTAATATAGGCTCAGCAGTGGAAGTCATCACAGTTGGGTAAACTT
Long Flanking Sequence:
AAGATCAAATTGCTAGGTGAAGATACTCAAATTCAGGAGAAAATGAATGGAGCTCAGGTATAGTAAGAGCCAAAGAGTGATATTCTAGTTCACTTACCAAATATCCACAAACATTCTGACTTACTCGCTGGCCTAAAATGTTTGTTTACTCTAGGGCATCCTGAACTCAGAATCAGAAGGAGATTATAAAATAGCCACCCTGAGAAGAAAAGTGGACGGTTTGTGCTCTCGAGAAAACCTGAGCGAGGACAGAAAACAGGAAGTCCAGCTAAACTTGAGGTCAGTTGAAGAGGAATGGAAGAAGGTCTTGGCTGGTGCTCAGCAACTAAAGAACCAGGCTGAGCTCCAGGATTCTCTTGCAAGGGAGCTTCAGACTTTTTATGCCCAGGAGGAGAGCACCTGGTCCTGGGTGAGGAACCAGAAGGATGTCCTGTACTCACTGGGGGAAAACACTCATGGTACACAAGACCAGCTTGAAGAGAGACTAAGCAGAGCACAAG[T/G]AAGTATTAATATAGGCTCAGCAGTGGAAGTCATCACAGTTGGGTAAACTTGGAGAGCAGTGAATGGGAGTTCTTTTTTCGCTTTCTAATTTGTTTACATAATAAAAGATTTAAAATACTGATAACTATATAATTATATCAATAGCTAAATTCTCATTTAAAATTACATTGCATTGTACGTGATCAAAATTTTCAGCTTATGCTAATTCTGAAAACGTAACCCTATATTAGTTTTTGAAGATCGGGAATTATGTAGCCAGAAGTACGTATGGCTGCATTTAGTTTTTAAAACGAACACTACCAGGCAGAATGACGTCGTTCCTTTTCAGGCGCACAGTACTAGCCAACCAGTTTGTCCAGTTAGCTTGCAATGTACGATGGTGAACTTGAGATGCAGAGAGGAGCTGACCATGACAACAGTGTTTGAGTACAGTGAAGAACGGTTCCAGAAAGCAGGTAAAACAAAACAGACGCCGAAAAATTTAATAAACAAGTAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8449
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 3496 | 9778 | 48 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37605655)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37082467 |
GRCz11 | 13 | 37208357 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGGGCCACTATGGAGGAGKKCATACCTGTCTTAATCAAAGAACTTACA[G/A]TAAGACATTTTTAGAGGAGTGCTGTGTTAATYATTTCTTACTAATTATGA
Long Flanking Sequence:
CAGGCTACTTTTTAGTTACTTTCAGATTACTTTTGAACTAATTAGTTTATCACATCAGTTGGGATTATTTTGTGCAATATTTATCTAAAAAATAAAAGAAATACATTCCATTCCTTATTAATATTTTTAAACAATCTTATTTATAATAATAATAGTAATAATAATACATTATCTTATTCCTCAGTCTTCTGAAAGGTTTAGTAGAGCGGCTGGTATCCTGTCAGTGTCAGAAGGAACAGCTTCAGTCTCGTCTGGAGCAAGTCAAAGAGCAGATATCTGCTCTTCCAAGGCGCTTCCCCTGGCCTGGTTTAGGGGATCGAAGACACACAGTGGAGCAAGCAAAGAGTCTGCTGGACCGCACCAGAGCCCTGAACCCATCTCTGTCTGCTGTCCGAGCACTCGGGAGGGAAATGAGCCAGCTGACCCGTGACTCCAACTGGATTGATCCATCATGGGCCACTATGGAGGAGTGCATACCTGTCTTAATCAAAGAACTTACA[G/A]TAAGACATTTTTAGAGGAGTGCTGTGTTAATTATTTCTTACTAATTATGACTAATAAATAGAAACCTGATTTACGTGTATGACCAATTTTTTGTTTGTGTGCTTGTGTAGGAGTTTTGTGTAAACCTTGAAGAGGAAATCCGGAGGGAGCGAGTTTGTGCTCAGTTGGTTGAGCAACACACCATGGCTCAGGATTGGCTGAGAGAGCAGGTCAAATGTTTTGGTGCTCTGCCCACTGAACGCCATGGGTTACAGGGCTCCATTAACACTCTTAAGGTCTGATTAAATTCTTATAATATATCTGGACTCTCACTTTTACACACAGTTGTAACAGTTTTACACAGTTTGCTAAGTTATACACTATAATACTCAGCTTGGAATAAAATTATCATGTTAATCTTTTAAAAATCTACTTTCCAGGCTCTTCTTCAGACTGTAGACAGGGAAAAGAGAGAAATGAAAGAGCTGAATGCTGTTAAAGATTCTCTGATGGACCTTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19067
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 3786 | 9778 | 53 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
ENSDART00000075522 | Nonsense | 3786 | 9778 | 53 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37603919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37080731 |
GRCz11 | 13 | 37206621 |
KASP Assay ID:
2260-6779.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTAAAAGCCTACAGGTGGCACTGTCTCATAAAGAACTGCTGAGGGACTG[T/A]CTAGGCCCTGACTTGGCTGGAAAGCTTGAAAGAGATGGCCTAAAAACACT
Long Flanking Sequence:
AGGTAAGTGTGTTAAAGCAGGATTGGAACTAAACTGTGCAAGGCTGCAGCTCCAGGAATTGGCTTTGACACCTGTGATGTATCACAATTATAGTGTAATGCTGCTTTAATTTAGAGTTAAATATTTATTGGAAAATTATTGATTTCCTTCAGTCTGCGATCGAAACTATCAGAGAGGCAGAATGACTGCGCAGACAGCACTGTGCAGTGTGTGAGACAGGCCTTACAAAACATTCAGTCATGGAACCAGATGGCAAATGCAAATCCTCCAACCAGCTCAGCCACATCCATGCAGGTGTGTTTGTGTCTTAATTTGCATGCAGTATATGAATACATAACAACACAACACACCTGCCTTATACATATATATATTTGATAGTAAGGTTGTTGTCACCTTGTGAACTGTAACATTTTTACTTCTTAGACTGCAATTGAGGAAGGAGCAAAACTGCGTAAAAGCCTACAGGTGGCACTGTCTCATAAAGAACTGCTGAGGGACTG[T/A]CTAGGCCCTGACTTGGCTGGAAAGCTTGAAAGAGATGGCCTAAAAACACTAAGTGAAGCAGACGCTTACATGAATGACATCAAACAGGAACTTAGGGTAAGTACATCTCATTTCTGTAGGATGATGTGATGACTGAACAAAATTTCTAGTGAGGTAAACAGAGGAGTTTGTGTTTCAGAATCTTCAGGAGAAGGTTGAGCAGGAGGCTCTGAGGTTGTCATTAGAGGCTCAAAACATTCAGGTTCACTCACAGGTACACATTTTAAAAAATGAAAGTGTATTTCTAGACTTTTAAAGTATTATTATGTGCAGCACTAATGTATGTTAAAAACAATTTGAAGGTTTCAACTGTGACACCATCAACAAAGGAGTCTGATCAATTGGAATTAGTTTCTTTTTCATCTTTTATTAATGAAAGCTGCAAAACAACGGATTACAGCGAACAGGCTAAGGTACAGCTATCTGAAAGCCTTGACAGCAATATACCTACATGTGTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9847
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 3786 | 9778 | 53 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
ENSDART00000075522 | Nonsense | 3786 | 9778 | 53 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37603919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37080731 |
GRCz11 | 13 | 37206621 |
KASP Assay ID:
2260-6779.1 (used for ordering genotyping assays)
KASP Sequence:
CGTAAAAGCCTRCAGGTGGCACTGTCTCATAAAGAACTGCTGAGGGACTG[T/A]CTAGGCCCTGACTTGGCTGGAAAGCTTGAAAGAGATGGCCTAAAAACACT
Long Flanking Sequence:
AGGTAAGTGTGTTAAAGCAGGATTGGAACTAAACTGTGCAAGGCTGCAGCTCCAGGAATTGGCTTTGACACCTGTGATGTATCACAATTATAGTGTAATGCTGCTTTAATTTAGAGTTAAATATTTATTGGAAAATTATTGATTTCCTTCAGTCTGCGATCGAAACTATCAGAGAGGCAGAATGACTGCGCAGACAGCACTGTGCAGTGTGTGAGACAGGCCTTACAAAACATTCAGTCATGGAACCAGATGGCAAATGCAAATCCTCCAACCAGCTCAGCCACATCCATGCAGGTGTGTTTGTGTCTTAATTTGCATGCAGTATATGAATACATAACAACACAACACACCTGCCTTATACATATATATATTTGATAGTAAGGTTGTTGTCACCTTGTGAACTGTAACATTTTTACTTCTTAGACTGCAATTGAGGAAGGAGCAAAACTGCGTAAAAGCCTACAGGTGGCACTGTCTCATAAAGAACTGCTGAGGGACTG[T/A]CTAGGCCCTGACTTGGCTGGAAAGCTTGAAAGAGATGGCCTAAAAACACTAAGTGAAGCAGACGCTTACATGAATGACATCAAACAGGAACTTAGGGTAAGTACATCTCATTTCTGTAGGATGATGTGATGACTGAACAAAATTTCTAGTGAGGTAAACAGAGGAGTTTGTGTTTCAGAATCTTCAGGAGAAGGTTGAGCAGGAGGCTCTGAGGTTGTCATTAGAGGCTCAAAACATTCAGGTTCACTCACAGGTACACATTTTAAAAAATGAAAGTGTATTTCTAGACTTTTAAAGTATTATTATGTGCAGCACTAATGTATGTTAAAAACAATTTGAAGGTTTCAACTGTGACACCATCAACAAAGGAGTCTGATCAATTGGAATTAGTTTCTTTTTCATCTTTTATTAATGAAAGCTGCAAAACAACGGATTACAGCGAACAGGCTAAGGTACAGCTATCTGAAAGCCTTGACAGCAATATACCTACATGTGTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38966
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 3986 | 9778 | 55 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37603150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37079962 |
GRCz11 | 13 | 37205852 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGCAGATAAAGAGATGCCCACTTCCTCATGCGCAGCTCCTGATAGCT[T/A]GGAAACCACAGTTCAAGACACAGACATTTGGAGCCGTGGAATTACAAGTC
Long Flanking Sequence:
AATGAAAGTGTATTTCTAGACTTTTAAAGTATTATTATGTGCAGCACTAATGTATGTTAAAAACAATTTGAAGGTTTCAACTGTGACACCATCAACAAAGGAGTCTGATCAATTGGAATTAGTTTCTTTTTCATCTTTTATTAATGAAAGCTGCAAAACAACGGATTACAGCGAACAGGCTAAGGTACAGCTATCTGAAAGCCTTGACAGCAATATACCTACATGTGTTATATCAGAAACTACAACAGAAGCAGAAGTTCATACTGCAAGAATATCACCACCAATAATAGAGAAAGATGTTAAAACATCTATACCACAGATTGCCACAGAGCTGCTATCTGAATCAGACACAAATGTTTATGAATCGGATGTTCCTGCTAGCAGCTATGGAGCTAATGAAGGTGAAAATGAGAAATTAATTTCTGTTGCTTTGGAAACAAAGGCTGATGAGAATGCAGATAAAGAGATGCCCACTTCCTCATGCGCAGCTCCTGATAGCT[T/A]GGAAACCACAGTTCAAGACACAGACATTTGGAGCCGTGGAATTACAAGTCTGAGTGCAAATGGACAAGAAAGTCAGATGTCTTTTGAAGTTGTGGGTTCAGACTTTTTTGCTGAAAGAGTGGAGGGTGAGAGCATCCAAGCAGTGATTGCAGAGCCGAATAAAGAGGAAGAAGGCTCATATATTTCACATTCTTTAGAAGAACCTGTTAGAGATAGTGTAGCGCAAACCAAAAAGGTTGCTTCGCTCATTTTAGATGAAGATACTGTATGCATACAGAGTTTAGACATACCTCCAGACAGTAATATTGCGAGGACAGACTCTGCTAGTGCCATGGTAAATGAGAAGACAGTGAGTCTTCAAACTATGGGAAAACAAGATGAAGAATCTTTGGCCCCTATAGAAGCTGAAATTTCTGAAAGGGCAATAGAAGCAATCCCCTTGCCATATTTTCCTAATGAGGCTGGTGTCATCAGTTTATCAGAAATTAGTTCTACAGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42258
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 4335 | 9778 | 55 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37602104)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37078916 |
GRCz11 | 13 | 37204806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATAAAGAACGATTTATAGAAACTGATTCTAAACTTAAACCTTCAGTC[A/T]AACAACCAAATGAGGGAGAAACTGAGGTTCAAACAAACAAGGTGGATATC
Long Flanking Sequence:
CACCTGCTGAAACACAAGATAGCGGAGATGCTGCTTCAAGAGGTATTGGAACATTTTCCTCAGACAATGGACCAAATGCTACAATTGCTGACAGTGAGGGCAGCTGGACTACAAATAATGGCCCCCGTGAAATCCAGCGTCGATATATTATTCTAGACTTGCCTGAGGGGGTGGAAATGCAGAGACATCACGCTCATGAAGGTACATCTTTAAGTGGATCCAGCGAGACACAGATTCAGGGATCAGGACATTCAGTAGCAGAAAGAATGGAGACAGAAGATGAGGCAGAATCTGCTGAAACTGAAACAGGTGCTTTAGTCAGCACAAACACAGTTTTGGAAGCACCAGAACAACATAAAACAATTGAAGCAGACCAAAACCTATCAACAAGGCAAGTTGAAGAAGATATGCATGTAATTCTAGATAAAGACACAAGAAAGACCCCATCAATGGATAAAGAACGATTTATAGAAACTGATTCTAAACTTAAACCTTCAGTC[A/T]AACAACCAAATGAGGGAGAAACTGAGGTTCAAACAAACAAGGTGGATATCTCCGTAACACCTGAAATGAAACCTGAAGGTAATAAGGCCATTGATGTCATTTTAGAAGCAGACACAATGGCTTCATCAGGTGGTAAAGCAAAATCCACAGTTATTGAACCTAAACTAACACCTCTGTTTCAGCAACTGACTGACAGGGACACTGAGATACAGTCCAAAAGAATGAATGTCATAATGACACCAGAAGAGACAAACAAGGCCCCATTAGTTGATGAAGCACAAATCATGGAATCGATACCTAAACTGATGCCTCCTGTCAAACGACAGGATAGTAAAACTGATGTCCAGTCAAACAAGATAAATGCATCAATGCAAGAGGAAAAAGCTGAAAATGAAAAAGGGATGGAAGTCATAAAACAAGAGACCTCATCAGGTGTAAAAGCACAGTCCATAAAAGTTAAACCTACAGTCATGCAATGGAATGATCAGGAAACTGAGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16713
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 4380 | 9778 | 55 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37601969)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37078781 |
GRCz11 | 13 | 37204671 |
KASP Assay ID:
2260-6777.1 (used for ordering genotyping assays)
KASP Sequence:
AGGCCATTGATGTCATTTTAGRAGCAGASACAATGGCTTCATCAGGTGGT[A/T]AAGCAAAATCCACAGTWATTGAACCTAAACTRACACCTCTGTTTCAGCAA
Long Flanking Sequence:
AGCGTCGATATATTATTCTAGACTTGCCTGAGGGGGTGGAAATGCAGAGACATCACGCTCATGAAGGTACATCTTTAAGTGGATCCAGCGAGACACAGATTCAGGGATCAGGACATTCAGTAGCAGAAAGAATGGAGACAGAAGATGAGGCAGAATCTGCTGAAACTGAAACAGGTGCTTTAGTCAGCACAAACACAGTTTTGGAAGCACCAGAACAACATAAAACAATTGAAGCAGACCAAAACCTATCAACAAGGCAAGTTGAAGAAGATATGCATGTAATTCTAGATAAAGACACAAGAAAGACCCCATCAATGGATAAAGAACGATTTATAGAAACTGATTCTAAACTTAAACCTTCAGTCAAACAACCAAATGAGGGAGAAACTGAGGTTCAAACAAACAAGGTGGATATCTCCGTAACACCTGAAATGAAACCTGAAGGTAATAAGGCCATTGATGTCATTTTAGAAGCAGACACAATGGCTTCATCAGGTGGT[A/T]AAGCAAAATCCACAGTTATTGAACCTAAACTAACACCTCTGTTTCAGCAACTGACTGACAGGGACACTGAGATACAGTCCAAAAGAATGAATGTCATAATGACACCAGAAGAGACAAACAAGGCCCCATTAGTTGATGAAGCACAAATCATGGAATCGATACCTAAACTGATGCCTCCTGTCAAACGACAGGATAGTAAAACTGATGTCCAGTCAAACAAGATAAATGCATCAATGCAAGAGGAAAAAGCTGAAAATGAAAAAGGGATGGAAGTCATAAAACAAGAGACCTCATCAGGTGTAAAAGCACAGTCCATAAAAGTTAAACCTACAGTCATGCAATGGAATGATCAGGAAACTGAGATCCAGTCAAAACAGTTGTATGTTTCACAAGATGGAAAGGCTAAAGATGAACAAACTATTCAGATTGCTGAGGAAAAAGATATGTATATGACTCCATTATGTGAAAAGACTCATTCCATAGAAGCCGAACCTAGACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42257
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 4451 | 9778 | 55 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37601755)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37078567 |
GRCz11 | 13 | 37204457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACTGATGCCTCCTGTCAAACGACAGGATAGTAAAACTGATGTCCAGT[C/A]AAACAAGATAAATGCATCAATGCAAGAGGAAAAAGCTGAAAATGAAAAAG
Long Flanking Sequence:
ACAACATAAAACAATTGAAGCAGACCAAAACCTATCAACAAGGCAAGTTGAAGAAGATATGCATGTAATTCTAGATAAAGACACAAGAAAGACCCCATCAATGGATAAAGAACGATTTATAGAAACTGATTCTAAACTTAAACCTTCAGTCAAACAACCAAATGAGGGAGAAACTGAGGTTCAAACAAACAAGGTGGATATCTCCGTAACACCTGAAATGAAACCTGAAGGTAATAAGGCCATTGATGTCATTTTAGAAGCAGACACAATGGCTTCATCAGGTGGTAAAGCAAAATCCACAGTTATTGAACCTAAACTAACACCTCTGTTTCAGCAACTGACTGACAGGGACACTGAGATACAGTCCAAAAGAATGAATGTCATAATGACACCAGAAGAGACAAACAAGGCCCCATTAGTTGATGAAGCACAAATCATGGAATCGATACCTAAACTGATGCCTCCTGTCAAACGACAGGATAGTAAAACTGATGTCCAGT[C/A]AAACAAGATAAATGCATCAATGCAAGAGGAAAAAGCTGAAAATGAAAAAGGGATGGAAGTCATAAAACAAGAGACCTCATCAGGTGTAAAAGCACAGTCCATAAAAGTTAAACCTACAGTCATGCAATGGAATGATCAGGAAACTGAGATCCAGTCAAAACAGTTGTATGTTTCACAAGATGGAAAGGCTAAAGATGAACAAACTATTCAGATTGCTGAGGAAAAAGATATGTATATGACTCCATTATGTGAAAAGACTCATTCCATAGAAGCCGAACCTAGACCAACTCCACCAGTAAGACGGAAGAATGACAATAAGGTTGATGCCCAGTCTTACAAGATGAATATCTCAACAACATCAGAGGATAGACCTGAAAATGTAGAGACCATGGCTCCATCAGATACTAAAACAAAAGCTTTAAAAGCAGAATCTGAACCAACACCACCAGTCAGGCAAAGGAATGAGGGGAAAACTGATGTCAAGGAACAATTCTCAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7376
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Missense | 6573 | 9778 | 68 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37581515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37058327 |
GRCz11 | 13 | 37184217 |
KASP Assay ID:
554-4076.1 (used for ordering genotyping assays)
KASP Sequence:
TGAATTGTGTATGTGTGATATACTGTACCTGCTGTAGGTGCGAGACTGGC[T/A]GCAGGAGCATGAKGACATGGTGAARGGCTCACAGAGCTGGATCTCAGAGG
Long Flanking Sequence:
TCTGTGGAAAATCAGCGGAATTCTGCGCGCGCAGATTCCGTGTGGCCCTAGACATGTCTTGATTGTTGATCAACAAGAGATGATGATTATTGGGTTAAACTTTCAGAATATGACTCCATTTAAGGGTATATTTCAACACTTTGGAAATGGACAGCGACTCCTAACGAGCACTTAGAACAAGTTCTTTTGGGGAAATGCACACAAAGTTTCAATGAGTGTTCAGATGCTCTTAAGAGCCAATATGCATTGTTATTGAGAAACCCAGCCCACGTCATGTAATTTTGATGCATCAAACAAAATAATTCATTTTCCTATGTGTAAGTTGGATTTCTTGCCCAAAGATTTTATAACTTCCAGAAATGATTGTAACTGGTTGGACTGGTTGGAAAGAAGTTGAAGATTAAAGTTGGAATTCAAGTAAAACAGGAGAATAGAAAATTAATTCCTAATTGAATTGTGTATGTGTGATATACTGTACCTGCTGTAGGTGCGAGACTGGC[T/A]GCAGGAGCATGATGACATGGTGAAGGGCTCACAGAGCTGGATCTCAGAGGCTCAGTCTTGGCTTACGACACCTTGCACATACACTACGGCCAGATGCCTGGACAGTCATGTGAATGCACTGCAGGTACTGTATTATTCTCAAACACATCATTATTTAGCTGATAATCACTTATTAGAGAGTAAGAAAACCAGAATCTTCGCATTAGCTATTCTTACATTCCCAAGAAATTATCTTGAAACGTGAATATACAGTAGAATAGTTTGTGTCCCATGTGTTCAAGTGAATACAAATGCCATTTCTTGGGGAACTAGCATGGCAAATCAATAATAATAAATATTAAATTTCTCCATAATAACTTTGCTGTGCCCCTGCCAGACGTCATATTCAATAGCAATTTATATGAAAAATATGTCTCTGTTGTAGTTTATGCTTGTATCCTTTTATCTGATACATAATTATCAAACTTGAATGGATACATACGTTTTAATGCACATTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11394
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 7162 | 9778 | 79 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37555972)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37032784 |
GRCz11 | 13 | 37158674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGGTGACGGTCCAGTTACAGCTGCAGGACAGACACAGCAACCATCAGG[T/C]ACACACGCACACTCTAATGCACAAAAYTTACTTCGCTTGCAAGAGMAGTT
Long Flanking Sequence:
TAAAAAAAAATTTTAAAAAGTAAAAACCACTGCTGTTGGATGTTCAAGTCAACAAACACTAATCGATCTCAATCTAAAGTCTGTCTGTTGGATTATTAATGAGATTTTTGTTCATATTTGTTTTTCTAAGACTGAGTCTTGGTTGAATGGAGCAGCATCTGTCAGCATCTTTAGTGCTTATTACTTTCCATTGTATCCTATTGTACCATGAACACCAGTAAGCATTTCTGTTTGCTTGACTGTATTCCTGCTGATTGCATTGGTTGTGTTGGAGTGATGCAGAGATGTTGTAGTTAGATGTTAATTGTGTGTTTGTTTTTTTTCATGAATCTAGACGACTCTGGTGGAGATCGAGCAGAGGATCTCCAGTCTTCCTCCATGTGGACTGAAAGAACAGGAGCAACACGAGGCTGAATCACTCAACACCAAACTCCAGCTCCTGAAGAACAGACTGGTGACGGTCCAGTTACAGCTGCAGGACAGACACAGCAACCATCAGG[T/C]ACACACGCACACTCTAATGCACAAAACTTACTTCGCTTGCAAGAGCAGTTCCTATACAATATGTTTCAGTAACAATTCATGCTACCTTTGTATATATACATATATATACAATTGAAGTTTAAGTTTAACGGAGATAAGATTTTTTCCGACACATTTCTAATATAATAAAAACATAATGCAATTCTAAGTATAATTGTTTGAGCTTTGACATGATGACAGTAAATAATATTTTACTAGATATTTTTCAAGACACTTCTATACAGCTTAAAATGACATTTAAAGGCTTAACAAGGTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCTATTTATTGTATAACTATGGTTTGTTCTGACTATTGAAAAAATAGCTTAAAGGGGCTAATAATTTTGTTCTTTAAATGGTGTTTAAAAAATGAGTAACTGCTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTGTCAGACTTATTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31952
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 7369 | 9778 | 85 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37547071)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37023883 |
GRCz11 | 13 | 37149773 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTTATTCATTCATTTATTCATACATTACTCTGGTTTTCTTTGAATTTC[A/G]GAGTTTATCTGTAGAGCTGATCTCCTTAGAGTCCACATTGAGCTCTCAGG
Long Flanking Sequence:
TTAGTTCTCTTTTTTTTCTTTAATTATACTTTTCAAAATAAATCCTCATTTCACTTAACAAGTTTACTATGATAATAAAGCTGGTTAACAAGTTTTTATTGTTTAATGAAGGAATTATAATGCGTTGTTTCATTATTTTACCTTCATTTACAAGTAGCAGAGTATTTACACAACTATTGTATTTTTCTATTTTGTACCTTTGTGCCCCCTGATGGCATAGTCGCAAACTGCGGTTATACCTAAAAACGTGTTAGTGCAGTGGCAGTGCCATTCACGTCGGTAATGCTCCTTTTAAAGTGTCACCCACTGTACATGAAACACAGTGATTACATATTGCTTTTTAAGTCAAATAGCATATCAAATATCGCATTATTTAGCATGCTATCACATATCGCGTTTTCCTTCAGTATCACACAGTCCTAGACTGATTTATCTGTCAGTCTGTTTACCACTTTATTCATTCATTTATTCATACATTACTCTGGTTTTCTTTGAATTTC[A/G]GAGTTTATCTGTAGAGCTGATCTCCTTAGAGTCCACATTGAGCTCTCAGGGGTCAGAGATCATGAAGTTATTAGTTTCAAGTTCATCGGTATCAGAGACATCCACCTGTTTTGATCTGCTGATGCAGCATGTGTGTGACATTCAGAAGACTCTGGCTGAGAAACAGGAGCAGCTACAGGAGAGAATAAAACACACAACTCAGCATCAGGTCAGATTTCTGTCTGCTTCAGTTTATTTCTTACCCATACAAACTAATGAGATTGATGTGCAGTTATGTAAAAAATGTTTGAAATTCTTGTAGCTTACAAGTTACTAGACATGCTAAAATTCAGGAAGTTGATTCTCATGTGTTAAAAGTGCTAATATTTCAGCAGTTTTAGCAGGCTTTAACACCCCAAACCCTCAATGCCTCATCCTAATAACTGTCATGAGCACTCAAACTTGTTTGGTTTGAAAAACACCATAAAACTTGTCTTCAGTCTCATGTTTAAAGGGATAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38965
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 7523 | 9778 | 88 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37543607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37020419 |
GRCz11 | 13 | 37146309 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGACACTTTGTGTAGGAGGTGTTGGAGAGTGTTTGGAGTGATCTAGAG[C/T]AGCGCTGTGGAGCTCTGCAGTGGACACTTGATCAGCAGCAGATGAGCCGA
Long Flanking Sequence:
TGTACTGCATGTCTTTGGACTGTGGTAGAAACCGGAGCACCCGGAGGAAACCCACGCAAATGCAGGGAAAAGATGCAAAACCCACACAGAAACGCTAACTGACTCAGCCGAGGCTCGAACCAGCGACCTTCTTGCTGTGACGCGACAGCACTACCTACTGCGCCACTGAGTCGTCCCTTATTTGGTCATTTATTTATTTATTTATAATTTTTTTTATTTATTTTTTACTTAAAATAATAAATAAATAAATAATACATCTGATTTCAAAGTTGATAATAATTGAACAACATCTACTTGAACCACAAACCATCATGTCATCTTTTGTACGGTACTGTGGTAATCTAAAAACTCAGCTTTGCCTTCAGAGAAATAAAGAACATTTTAAAATATATTAAAATAGAATGTAGTTATGTGAAATAATGTCTTTTTGATTGTGTATATTCTAATATAATGGACACTTTGTGTAGGAGGTGTTGGAGAGTGTTTGGAGTGATCTAGAG[C/T]AGCGCTGTGGAGCTCTGCAGTGGACACTTGATCAGCAGCAGATGAGCCGAAAAATACTGAAGGCTCTGCAGATGCTATTGAATCTTGGAAAAGAGAAACTCACCAGCATGCCTCAAATAGAGCTTGGAAATACAGCACAACTACAGACACAACTCAACACACACACGGTAAAGCCTATCACTTTAAATGCACACATACAGCCCTTAAAACAGCAAATCAACACTATCATTAAAGTGTCTGTGATCTCTCATTCATCTCTTTGTAAATATAGTCGTTTTTCCAATCTCTGAGTGGCCACCTGAGGAGACTTCAGCAACTGAGTGTACGGATGCCACACAGCGCCTCCTCTGGCTGGGAGACTGAAGTGTCTGAGATTGAATGTCAAGTTTCCAGTGTTTTACAGCAGGCTCAGGCTGTGGGTACATTGCTGCACTCAGCACTGCAGGTACGAGAGCAAGGGGATTCTTCTATAAGCACTTCTGATGCACAGTCTATGCGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22355
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 8345 | 9778 | 101 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37533742)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37010554 |
GRCz11 | 13 | 37136444 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATCTTATTGTCTTTGTTTAGGTGTTACAGAAAGGCTCAGAGATGCTA[C/T]AGACTGATGTGAATGAAATGCTTGAAGCCTCTAAAGATGTGATTGAACAG
Long Flanking Sequence:
TAGTTGTATTATTTTTTCATCTTAAGCTCTATTATTGGGCATCACACAGGACTGGGTTGAATACATGACATGCTTTAGAGATGTTTTGATGGAGTACATGTTAGTGTCAGAGTAATTCCATCTATATGTAAGAATGAACTGTATCTTAAATCAGTCCTGTCTGCTGCTATCAGGCTTTTCAGTGTGCAAAAATTATTATGGAATTTGTTGCTTAATGTGCAATATACCTGTATCACAAGCCTATTATCATGAAATATTTAATTTTTTATAATTTTATTCCTAATATAATATATTAAAATATATAATATAATATAATATATAATAAAATAATAAAATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATAATATATTTTGGGTCTCAGTATATCACACATCTTATTGTCTTTGTTTAGGTGTTACAGAAAGGCTCAGAGATGCTA[C/T]AGACTGATGTGAATGAAATGCTTGAAGCCTCTAAAGATGTGATTGAACAGATGAATGAAGAAGATGCTGTTTTCATCCGATCTGAATGCCGTTTGATCACACGTGGTTACCTGCAGTTAAAACAGACTCTTACAGGACGAATTGAACACATGCAGGTAAGACTCAAATGCAGGACTTTCTTATCTAGTGAAAGTACCGGAACAAATTTTATTAAAATACACATTCTGGCGTTATTTATTTACTCCCTCTCATATCAGTCCGAACACTCTCTTGTACGTTTTTTCATGAGAAACATTTGGCTGAAAAAGCTCTAGAATACACTTTAAATATGAAATTTTTAATAATTTTTATACTTATTTTAACCTGTTTCAAATAAGTATAAAATATTTTATATTTTATATTTAAAGGATATTACAGTAGGTCCAATAGATATTTGCATTCATTTGTTCCAACTGCAGTTGAGTTTATTAATAAGCTTTTTGTCGTATTTTGGTTATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6326
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 8386 | 9778 | 101 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | None | None | 1153 | None | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37533619)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 37010431 |
GRCz11 | 13 | 37136321 |
KASP Assay ID:
554-4614.1 (used for ordering genotyping assays)
KASP Sequence:
TCATCCGATCTGAATGCCGTTTGATCACACGTGGTTACCTGCARTTAAAA[C/T]AGACTCTTACAGGACGAATTGAACACATGCAGGTAAGACTCAAATGCAGG
Long Flanking Sequence:
ATATGTAAGAATGAACTGTATCTTAAATCAGTCCTGTCTGCTGCTATCAGGCTTTTCAGTGTGCAAAAATTATTATGGAATTTGTTGCTTAATGTGCAATATACCTGTATCACAAGCCTATTATCATGAAATATTTAATTTTTTATAATTTTATTCCTAATATAATATATTAAAATATATAATATAATATAATATATAATAAAATAATAAAATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATAATATATTTTGGGTCTCAGTATATCACACATCTTATTGTCTTTGTTTAGGTGTTACAGAAAGGCTCAGAGATGCTACAGACTGATGTGAATGAAATGCTTGAAGCCTCTAAAGATGTGATTGAACAGATGAATGAAGAAGATGCTGTTTTCATCCGATCTGAATGCCGTTTGATCACACGTGGTTACCTGCAGTTAAAA[C/T]AGACTCTTACAGGACGAATTGAACACATGCAGGTAAGACTCAAATGCAGGACTTTCTTATCTAGTGAAAGTACCGGAACAAATTTTATTAAAATACACATTCTGGCGTTATTTATTTACTCCCTCTCATATCAGTCCGAACACTCTCTTGTACGTTTTTTCATGAGAAACATTTGGCTGAAAAAGCTCTAGAATACACTTTAAATATGAAATTTTTAATAATTTTTATACTTATTTTAACCTGTTTCAAATAAGTATAAAATATTTTATATTTTATATTTAAAGGATATTACAGTAGGTCCAATAGATATTTGCATTCATTTGTTCCAACTGCAGTTGAGTTTATTAATAAGCTTTTTGTCGTATTTTGGTTATGAATATTGGATACTCCTGCAGTTTGAACATGTTTTGATTGGTAACACATTATATACCATTTTATTTGATTACAATTCATTTGAATGTTTATTATTAACTTTAGTTTATTTATTGCTGTGAACCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8857
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 9050 | 9778 | 114 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | Nonsense | 397 | 1153 | 8 | 22 |
ENSDART00000135935 | None | None | 207 | None | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | None | None | 252 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37503082)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36979894 |
GRCz11 | 13 | 37105784 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCGCCTAWGGTGCAAGTTCCTGGACGATTATGCWCGTTTTGAAGAGTG[G/A]CTGAACACAGCAGAAAGAACAGCTGCCAACCCCGCCACCAAAGATGTGCT
Long Flanking Sequence:
TATTAAACAGATTCTATCAACACATTTTATTGCACCTTTAATAAATACTGTAACAAATCTTTTGCTCATTGTATGTTAAAGTTTGTTGCTGCATAAACTAATGGAACCATATCAACTTACAGTTTTTTGGTATCTTCCAGAGTGTGATTGTGTTTGTGTCCTTCAGGACTTGCAGAGAGATATTGAACAGCACACAGAGGGTGTAGCGTCTGTTCTGACACTGTGTGACGTTTTGCTGCATGATGCGGACGCTTGTGGGAGTGATGGAGAGAACGACTCCATTCAGCAGACCACACTCAGCCTGGACCGCCGCTGGAGGAATATATGTGCCATGTCTATGGAGAGGAGAATGAGGTCAAAATCCACATATTTGACTGCATCTGTGTCTAAGTTCTATTAGTTTTTCTAACACCTGTACTCTATACTGTCCCCTGCAGGATTGAGGAGACATGGCGCCTATGGTGCAAGTTCCTGGACGATTATGCTCGTTTTGAAGAGTG[G/A]CTGAACACAGCAGAAAGAACAGCTGCCAACCCCGCCACCAAAGATGTGCTCTACACCTGTGCTAAAGAGGAACTCAAAAAGTTTGAGGTTTGATTCTTTTTAGTTCATCGTAGTGCAGTATATGAAATAACAGCAGAAGTACTATAGATAGTTCAGATGTAAATTTTGTATTTTGATTACCTGATGAATAGATTAACTGTTTTTTAAACATGCGCACATGCAGGCATTTCAGCGTCAGGTCCACGAGCGATTGACACAACTGGAACTGGTGAATAAACAATATCGGCGTCTGGCGCGAGAGAACCGGACTGATGGAGCCAGTAAACTGAAGCTGATGGTGCATGAGGGAAACCAGCGCTGGGATACACTACAGAAGAGAGTGGCCGCTGTGCTTCGCAGGTTAAAGGTCAGAAAATTACATCTGTTCATATGTCACAACATTAAGACCATCCTTTATTAAGAAGCCATTTATGTGAGATTGAAAGCTGGAGTAAGGATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22354
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 9301 | 9778 | 118 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | Nonsense | 648 | 1153 | 12 | 22 |
ENSDART00000135935 | Nonsense | 64 | 207 | 2 | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | Nonsense | 33 | 252 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37499725)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36976537 |
GRCz11 | 13 | 37102427 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTGCCATGGGCTGTGATGTGTCGTTAACTGTACGTCAGGCTGTTTCA[C/T]AGCTATTACCGCCTGCTTTGGAGCGCTCAGGCCGTGAGACGCCTGTCAGT
Long Flanking Sequence:
TATAAATGAAAATAGAAGTTATATATACAAACATAAAAAAAACATAGAAGTATTCCTAAAAAAATGCCTGGTGCATTATGACAGGAAGAGTGATGTCCTACGGGTGGTTTGTCAAGCCCACTCACCTACATGGAGCACACTCATGCATCCTACAGTTAGGTGATGCATTGTATATATGTTTACTAAAGAAAACTAGATCTTTAATTTAGTTTTGAACAGAGAGAATGTGTCTGAGCCTCAGAAGCTATCAGGAAGGCTATTCCAGAGTTTAGGAGCCGTATATAAGAAAGCTCGACCTCCTTTAGTGGACTTTGAATACTGATTTACCTCTTTAATCTCTTGGTTTTTTACAGGTTCTTGAAGAGGAGCGTGAGTTCTCGGACAGAGACACAGATCCGGAGGACTCTGCTGATTTCGGTGGGGTGTGGGAGAGGGAAAGAGAGGAAGAGGAGGCTGCCATGGGCTGTGATGTGTCGTTAACTGTACGTCAGGCTGTTTCA[C/T]AGCTATTACCGCCTGCTTTGGAGCGCTCAGGCCGTGAGACGCCTGTCAGTGTGGATTCAATTCCGCTGGAGTGGGATCACACTGTGGATGTGGGAGGATCTTCTTCTCCGGAGGAGGATGAGGAGTTGACCTACTACAGCGCTCTGTCAGGTAACGCTTTACTGACTGATCTCTGACAATACTTTTCTTAGATCTCTCTGCGTGATGTATGAATAATACTGCATTTTAGAATACATTTTCACCTCTTGTGAAATTTGAATTCTTTAAAAATATTTCCCAAGTGCTGTTTAACAGAGAATATTTGTTCAACACATTATTAAACACAATAGTTTTAATAACTTATTTCTAATAGCTACTTTCTTTTGTTTTTTAATTTGATGACAGTATTTTAGTAGTTATTTTGCAAGGTACTAGCATTCAGCTTAAAGTGTTGCACTCACTTTTGGGGTTTACACTTACTTGAATTTAAATAGTAATTGTTCTTGAGCCCAGTGAGCTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22353
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Nonsense | 9396 | 9778 | 120 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | Nonsense | 766 | 1153 | 15 | 22 |
ENSDART00000135935 | Nonsense | 159 | 207 | 4 | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | Nonsense | 128 | 252 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37490962)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36967774 |
GRCz11 | 13 | 37093664 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACTACTCCACACAGACAGTATAATGTTGTACTTTGTCTCTCCAGGAT[A/T]AACTGATGTCCGAGTGTGCGGGCAGTATAGACAGTATAAAGCGAGTCAAG
Long Flanking Sequence:
TTTTTGTTTGAAAATGTAGTCCATGCCTATTTTCTAACCCTAAACCCAACCAAAACTGTAAATTATTCCCAAGATCAGAAGTGAATAATAGTTGGATAACAATTGTGTAGAAGTGTATAAACCTAACTATAAGCCTAAACTTAACATAAATGGTAAACATATCCCTTAATTCTGATTGGCTGATTGGAATGTTGTTCCAGGATCAACATAGATCTTAAACCAGGAACTTGTCCTACTTGGTGAAATCTGTTTGGCTAAAGTCAACAAATCACTTTAACAGCAACAGGTTTACTCATTTTTTTCAAGTACAGTCAACAAATCACTTTTTTCCAGTGTACATTATTGTTTCTTTCCATTTATTTGCACTACATATTCATTAATGATGTCAAAAACTATCCTCAAATGCAGTTAACCATTTGTGTACAATCTCCCAATTTTTATGCTGGGTAAAGCACTACTCCACACAGACAGTATAATGTTGTACTTTGTCTCTCCAGGAT[A/T]AACTGATGTCCGAGTGTGCGGGCAGTATAGACAGTATAAAGCGAGTCAAGCTGATTCTGAATGAGGATGAACAGCTGGAGGATCAGGGTCTGACGGGCTTCAGTGCAGCAGATAACACAGGTACTGCTGATTACATCAAGCACACACACACACACACACACACATAAGCAAACACACACCTTTACAGAGATTTATGGGCTAATTTTTTAAAGATGGTCTGTGTTCAGGTGTGATCGAGCGGTGGGAGCTGCTTCAGGTGCAGTCGTCTCGCGTCCCGCAGGATCTTCAGCACTGGCACAGACTGAACTCTGACCTCTCTGACATTATGGTATGGCTGAACGCTGTGATGCCTGAACTGGAGACATTGCAGACTCTAGAGGCCAAAATCACCATCAGAGACATGGAGAGCAAGATCCACAAACTGAAGGTATATCAAGACATTAAAGTTCATTAAGCAAAAAGAAGCCATTCAGGCTCAGCTATTGTATTGAGTGCTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9190
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 |
---|---|---|---|---|---|
ENSDART00000075522 | Essential Splice Site | 9436 | 9778 | 120 | 127 |
ENSDART00000133242 | None | None | 273 | None | 5 |
ENSDART00000135510 | Essential Splice Site | 806 | 1153 | 15 | 22 |
ENSDART00000135935 | Essential Splice Site | 199 | 207 | 4 | 5 |
ENSDART00000136750 | None | None | 168 | None | 4 |
ENSDART00000139734 | None | None | 281 | None | 7 |
ENSDART00000147884 | Essential Splice Site | 168 | 252 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 37490840)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 36967652 |
GRCz11 | 13 | 37093542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCTGGAGGATCAGGGTCTGACGGGCTTCAGTGCAGCAGATAAYACAGG[T/C]ACTGCTGATTACATCAAGCACACNNNNNNNCACANNNNNNNNNNNGCAAA
Long Flanking Sequence:
CTAACTATAAGCCTAAACTTAACATAAATGGTAAACATATCCCTTAATTCTGATTGGCTGATTGGAATGTTGTTCCAGGATCAACATAGATCTTAAACCAGGAACTTGTCCTACTTGGTGAAATCTGTTTGGCTAAAGTCAACAAATCACTTTAACAGCAACAGGTTTACTCATTTTTTTCAAGTACAGTCAACAAATCACTTTTTTCCAGTGTACATTATTGTTTCTTTCCATTTATTTGCACTACATATTCATTAATGATGTCAAAAACTATCCTCAAATGCAGTTAACCATTTGTGTACAATCTCCCAATTTTTATGCTGGGTAAAGCACTACTCCACACAGACAGTATAATGTTGTACTTTGTCTCTCCAGGATAAACTGATGTCCGAGTGTGCGGGCAGTATAGACAGTATAAAGCGAGTCAAGCTGATTCTGAATGAGGATGAACAGCTGGAGGATCAGGGTCTGACGGGCTTCAGTGCAGCAGATAACACAGG[T/C]ACTGCTGATTACATCAAGCACACACACACACACACACACACATAAGCAAACACACACCTTTACAGAGATTTATGGGCTAATTTTTTAAAGATGGTCTGTGTTCAGGTGTGATCGAGCGGTGGGAGCTGCTTCAGGTGCAGTCGTCTCGCGTCCCGCAGGATCTTCAGCACTGGCACAGACTGAACTCTGACCTCTCTGACATTATGGTATGGCTGAACGCTGTGATGCCTGAACTGGAGACATTGCAGACTCTAGAGGCCAAAATCACCATCAGAGACATGGAGAGCAAGATCCACAAACTGAAGGTATATCAAGACATTAAAGTTCATTAAGCAAAAAGAAGCCATTCAGGCTCAGCTATTGTATTGAGTGCTTTTCGATTTTGTCCAGGCCAGATTTATTAGGTTGCCTTTTATTAATGCTTCTGTTAAACCACAATTTAAAAAGCAATATCAGATTTTTTTTAGTTTGTTGTCATTTTTAATTAATCTTTACTTTTT
Associated Phenotype:
Not determined