Busch Lab

ZMP

BSN (2 of 2)

Ensembl ID:
ENSDARG00000079822
Description:
bassoon (presynaptic cytomatrix protein) [Source:HGNC Symbol;Acc:1117]
Human Orthologue:
BSN
Human Description:
bassoon (presynaptic cytomatrix protein) [Source:HGNC Symbol;Acc:1117]
Mouse Orthologue:
Bsn
Mouse Description:
bassoon Gene [Source:MGI Symbol;Acc:MGI:1277955]

Alleles

There are 26 alleles of this gene:

Allele Name Consequence Status Availability
sa21405 Nonsense Available for shipment Available now
sa16623 Nonsense Available for shipment Available now
sa14012 Nonsense Available for shipment Available now
sa41317 Essential Splice Site, Missense Mutation detected in F1 DNA Not yet available
sa41316 Essential Splice Site, Splice Site Mutation detected in F1 DNA Not yet available
sa13749 Nonsense Available for shipment Available now
sa8919 Nonsense Mutation detected in F1 DNA Not yet available
sa11540 Nonsense Available for shipment Available now
sa9997 Nonsense Available for shipment Available now
sa34527 Nonsense Mutation detected in F1 DNA Not yet available
sa21404 Nonsense Available for shipment Available now
sa45341 Nonsense Mutation detected in F1 DNA Not yet available
sa21403 Nonsense Available for shipment Available now
sa2454 Nonsense F2 line generated Not yet available
sa7284 Nonsense Mutation detected in F1 DNA Not yet available
sa21402 Nonsense Available for shipment Available now
sa25413 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa7165 Nonsense Mutation detected in F1 DNA Not yet available
sa41315 Nonsense Mutation detected in F1 DNA Not yet available
sa30911 Nonsense Mutation detected in F1 DNA Not yet available
sa34526 Nonsense Mutation detected in F1 DNA Not yet available
sa11595 Nonsense Available for shipment Available now
sa44694 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21405
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 20 3782 1 18
ENSDART00000114444 None None 3719 None 19
ENSDART00000122421 None None 3727 None 19
Genomic Location (Zv9):
Chromosome 8 (position 55824557)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53943145
GRCz11 8 53811639
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGGAGGTCCACCAACAAGTCCAAAACTAGGCTATGGAGCTGGTAGTGAT[C/T]GAGGGCCGGGTGCTGACTTTGGCACGGGTGGAATGCAAACAAGTGCAAAC
Long Flanking Sequence:
AGCACCCAGAGAAAACCCACGCGAAGGCAGGGAGAACATGCAAACTCCACACAGAAACACCAACTGAGCTGAGGTTCGAACCAGCGACCTTCTTGCTGTGGGGCGACAGCACTACCTACTGCGCCACGGCCTCGCCTTCCACTGCATTATGTGATTACCATTTTAAAATGTTTAAAAATTCAGTGTTTGTCCACTGGGGGGCGATCTGTGTAATCCAATAAAACCCAGATGAATCATGCAAGCTCACTGAGATCACCACCTAAGTGGCAAACAGGTTTCTTAGGTGTTTAATCTGATTGCAGATCATATATATTAGTTTGTAGACTTTCTAATGACACATTTATGAAATGAAAAGGAATAATAGTTAGGAGTCTCTTGTTTAAAAAATCCCCACTGGCAATACTCATGTGTTCTCATCTTCTTGTTTTGTCTTATTTAGGTTGGCTGGAGCGGGAGGTCCACCAACAAGTCCAAAACTAGGCTATGGAGCTGGTAGTGAT[C/T]GAGGGCCGGGTGCTGACTTTGGCACGGGTGGAATGCAAACAAGTGCAAACCCTTACAAAAAGCAAATCCATGATGGACCCAGACATTCCCAGACTACGCCTACGCATCAGTCTCAAATTCAAGCTTCAGCAGGGGGCATGGGAGCCAACCAGAGCCCGGGCCAGCACGCCTCCAGACGCAACCTCCAAGTGGACTTCAGCAGTAGCAGCAGAACGGGACGCTCCCCGTCAGCGTCTCCTGACAGAACTAGTGCACCGACTTCACCATACTCCGTACCCCAGATCGCACCGATGCCTAGCAGTAAACTCTGTCCAGTCTGCAATACAACAGAGCTGACCAATTTTGACGGGTCGCCGAACTTCAACAAGTGCACACAGTGCCACACTACAGTGTGCAACCAGTGCGGCTTCAACCCCAACCCACACCTTACAGGGGTAAGACTTCTGCAGAAATGGGATCTATTTATCAACATCTGTATGACTTGGCATGATGTGAATTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16623
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 45 3782 1 18
ENSDART00000114444 Nonsense 16 3719 1 19
ENSDART00000122421 None None 3727 None 19
ENSDART00000111967 Nonsense 45 3782 1 18
ENSDART00000114444 Nonsense 16 3719 1 19
ENSDART00000122421 None None 3727 None 19
Genomic Location (Zv9):
Chromosome 8 (position 55824482)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53943220
GRCz11 8 53811564
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGTGGAATGCAAACAAGTGCAAACCCTTACAAAAAGCAAATCCATGAT[G/T]GACCMAGACATTCCCAGACTACRCCTACGCATCAGTCTCAAATTCAAGCT
Long Flanking Sequence:
TCGAACCAGCGACCTTCTTGCTGTGGGGCGACAGCACTACCTACTGCGCCACGGCCTCGCCTTCCACTGCATTATGTGATTACCATTTTAAAATGTTTAAAAATTCAGTGTTTGTCCACTGGGGGGCGATCTGTGTAATCCAATAAAACCCAGATGAATCATGCAAGCTCACTGAGATCACCACCTAAGTGGCAAACAGGTTTCTTAGGTGTTTAATCTGATTGCAGATCATATATATTAGTTTGTAGACTTTCTAATGACACATTTATGAAATGAAAAGGAATAATAGTTAGGAGTCTCTTGTTTAAAAAATCCCCACTGGCAATACTCATGTGTTCTCATCTTCTTGTTTTGTCTTATTTAGGTTGGCTGGAGCGGGAGGTCCACCAACAAGTCCAAAACTAGGCTATGGAGCTGGTAGTGATCGAGGGCCGGGTGCTGACTTTGGCACGGGTGGAATGCAAACAAGTGCAAACCCTTACAAAAAGCAAATCCATGAT[G/T]GACCCAGACATTCCCAGACTACGCCTACGCATCAGTCTCAAATTCAAGCTTCAGCAGGGGGCATGGGAGCCAACCAGAGCCCGGGCCAGCACGCCTCCAGACGCAACCTCCAAGTGGACTTCAGCAGTAGCAGCAGAACGGGACGCTCCCCGTCAGCGTCTCCTGACAGAACTAGTGCACCGACTTCACCATACTCCGTACCCCAGATCGCACCGATGCCTAGCAGTAAACTCTGTCCAGTCTGCAATACAACAGAGCTGACCAATTTTGACGGGTCGCCGAACTTCAACAAGTGCACACAGTGCCACACTACAGTGTGCAACCAGTGCGGCTTCAACCCCAACCCACACCTTACAGGGGTAAGACTTCTGCAGAAATGGGATCTATTTATCAACATCTGTATGACTTGGCATGATGTGAATTTGCCTTGGCAGTAGATATTCGATCATTGTTGCAGATATAGAATGCCAGTCAGAGCTCGGTAGATCATTTAGGAGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14012
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 45 3782 1 18
ENSDART00000114444 Nonsense 16 3719 1 19
ENSDART00000122421 None None 3727 None 19
ENSDART00000111967 Nonsense 45 3782 1 18
ENSDART00000114444 Nonsense 16 3719 1 19
ENSDART00000122421 None None 3727 None 19
Genomic Location (Zv9):
Chromosome 8 (position 55824482)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53943220
GRCz11 8 53811564
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGTGGAATGCAAACAAGTGCAAACCCTTACAAAAAGCAAATCCATGAT[G/T]GACCMAGACATTCCCAGACTACGCCTACGCATCAGTCTCAAATTCAAGCT
Long Flanking Sequence:
TCGAACCAGCGACCTTCTTGCTGTGGGGCGACAGCACTACCTACTGCGCCACGGCCTCGCCTTCCACTGCATTATGTGATTACCATTTTAAAATGTTTAAAAATTCAGTGTTTGTCCACTGGGGGGCGATCTGTGTAATCCAATAAAACCCAGATGAATCATGCAAGCTCACTGAGATCACCACCTAAGTGGCAAACAGGTTTCTTAGGTGTTTAATCTGATTGCAGATCATATATATTAGTTTGTAGACTTTCTAATGACACATTTATGAAATGAAAAGGAATAATAGTTAGGAGTCTCTTGTTTAAAAAATCCCCACTGGCAATACTCATGTGTTCTCATCTTCTTGTTTTGTCTTATTTAGGTTGGCTGGAGCGGGAGGTCCACCAACAAGTCCAAAACTAGGCTATGGAGCTGGTAGTGATCGAGGGCCGGGTGCTGACTTTGGCACGGGTGGAATGCAAACAAGTGCAAACCCTTACAAAAAGCAAATCCATGAT[G/T]GACCCAGACATTCCCAGACTACGCCTACGCATCAGTCTCAAATTCAAGCTTCAGCAGGGGGCATGGGAGCCAACCAGAGCCCGGGCCAGCACGCCTCCAGACGCAACCTCCAAGTGGACTTCAGCAGTAGCAGCAGAACGGGACGCTCCCCGTCAGCGTCTCCTGACAGAACTAGTGCACCGACTTCACCATACTCCGTACCCCAGATCGCACCGATGCCTAGCAGTAAACTCTGTCCAGTCTGCAATACAACAGAGCTGACCAATTTTGACGGGTCGCCGAACTTCAACAAGTGCACACAGTGCCACACTACAGTGTGCAACCAGTGCGGCTTCAACCCCAACCCACACCTTACAGGGGTAAGACTTCTGCAGAAATGGGATCTATTTATCAACATCTGTATGACTTGGCATGATGTGAATTTGCCTTGGCAGTAGATATTCGATCATTGTTGCAGATATAGAATGCCAGTCAGAGCTCGGTAGATCATTTAGGAGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41317
Status:
Mutation detected in F1 DNA
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, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Essential Splice Site 288 3782 2 18
ENSDART00000114444 None None 3719 None 19
ENSDART00000122421 Missense 212 3727 2 19
Genomic Location (Zv9):
Chromosome 8 (position 55821007)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53946695
GRCz11 8 53808089
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTGGCCCTACTGGACCTAGCCAGACTGGATTTTACAGCGGGCCACAA[A/G]CTGGACTCCAAACACAAAAAGAGCCACCACAAGCAGGACATTTACAATCA
Long Flanking Sequence:
GCCTGAACTCTGCACATTGTGCGATTTATGAAATGCCTAATCTTTAGTCCGTAGCCAATTAGTTTTAGCCAAAGGCAATCAGAATGATGTATATCTGTCTCTGAGTACTGCCTTTATTTCATTAACAGGTCAAGGAGTGGCTCTGTCTAAACTGCCAAATGCAGCGGGCTTTGGGAATGGACATGACAACACCACGGTCCAAGAGTCAGCAGCAGATACATTCTCCCTCTCATCAACCCAAGCCTGACCCAATACCCAAGACCCAGCCCTCAGCGCAACCCACACCACAGATACAACCCCAAATGCAGACACAGATGAAAATTCAGCCACAACCACATCCACAACCTCAGCCACATCAGCAGCCTCAGCCACATCCACAGCCACATCCACATCCACAACCTCAGCCACATCCACAGCCTCAACCTCATGCTGTTTCTGGGATCCAAAGACAGACTGGCCCTACTGGACCTAGCCAGACTGGATTTTACAGCGGGCCACAA[A/G]CTGGACTCCAAACACAAAAAGAGCCACCACAAGCAGGACATTTACAATCAGGTTACCAGTCAGAGCCCCAAAGGCAAGTACTGGGACCAAAAAGTCCAGAAAGGGGGCCCCAAATAGGACGTATTCCTCATCCGGGTGCGGTGCCTTTACCTGGTTTAGCAAAGGCACAGTCACAGTCGGATCTCGGACGTGGATCTCCGGTGCGGATTGGAAGTCAACCGGATCGAACTCGAAGTGCTGGAAGCTCCCCAGCTCATCATGCACCATCCCATGATCCACCTCAGGATGGTCTAACTAAGCTGTTCGGTTTTGGGGCTTCCTTACTAAACCAGGCGAGCACTCTTATTTCTGTCGATCCTCTTACTGGATCCTCACAGCCGTCGCCTGCGCGGAACCAGAGTGCGCAGGGGACAAAGGTGATCTTTAGTGATGCTAATTCTGGAGCTAGTGCAAAAACCACAGCAGGACCTCCTGGGGCTTTCAAAACAGGTCCAGGAGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41316
Status:
Mutation detected in F1 DNA
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, Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Splice Site None 3782 None 18
ENSDART00000114444 None None 3719 None 19
ENSDART00000122421 Essential Splice Site 537 3727 6 19
Genomic Location (Zv9):
Chromosome 8 (position 55815883)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53951819
GRCz11 8 53802965
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATTAGCATGTTTGGATTGAAGGAAATGTTTTTGAAACTTGTTATTGG[T/C]TAGCATTTTTAAACTTAAAGCAAAACCCTGTGTGTTAAGACTTTAATGCG
Long Flanking Sequence:
GAATGGCTCTGTCTGAACTGTCAGACTCAGAGACTAATGTCTGGTGGACTCGATCCTGTTCCAGTCGCACCATCATCTCCCAGTCGCCAACCGTTGGGTTCTCCGCGCCATCAGCAAATTTCCAGCAAGCAGCAAGGGACACCACAGCAGAAACCCCCAGTTTCCCAACAAAGTGCATTTTCAAGTGATATGAAGACATCTACTGCGCTAACCACAACCACCACACCTCCTGTGTCCATCACTGCTGCGTTTGCCGGTGGAGAAGAGAGAAAAGAATACACACCCAAGCTGGACAAAGAGCTTGAGGATAAAGAAAATACACTGGCTCAGAAGAGAGGAACAGCCGAGTCCATTCAGATGATTTCTAAAGACGAAAAGAAAGAATTGCAGAGCATCACTAAATACTATGAGGTAAGCGTGTTTGGGTTACAGTCATTCTCCATTGTTTTATAAATTAGCATGTTTGGATTGAAGGAAATGTTTTTGAAACTTGTTATTGG[T/C]TAGCATTTTTAAACTTAAAGCAAAACCCTGTGTGTTAAGACTTTAATGCGTATATAAAGGCCACTTTATTAGGTACACCTTACTAGTACCGGGTTGGACCCTTTTTGCCTTCAGAACTGCTTTAATCCACGGTGTCAGAGATTCAGCAAGCTACTGGAAATACTCCTCAGAGATTTTGCTCCATATTGTCATGATAGCATCACACAGTTGCTGCAGATTTGTCAGCTGCACATCCATGATGCCAATCTCCCGTTCCACCACATCCCAAAGCTGCTCTATTGGATTGAGGTCTGGTGACTGTGGAGGCCATTTGAGTACAGTGAACTCATCGTCATGTTCAAGAAACCAGTCTGAGATGATTGAGCTTTATGACATGCTGCATTATCCTGCTGGAAGTAGTGCTCATAAAGGCATGGGCGTGGTCCAGAACATAGATTTACAGTCGGTTTTCATCGCCCCTAGTTCTTTGACTGACTCAGTATGTTTCAGCCATAATTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13749
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 1077 3782 8 18
ENSDART00000114444 Nonsense 1021 3719 9 19
ENSDART00000122421 Nonsense 1006 3727 9 19
Genomic Location (Zv9):
Chromosome 8 (position 55812197)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53955505
GRCz11 8 53799279
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCAAGCTGTACAAATCTGGTAGTGAGTACAACCTGCCCACCTTTATGT[C/A]ACYTTATTCTCCTACTGAAAAGCCAGAAACTACATCATCTACTGCTGCTG
Long Flanking Sequence:
CACCTCTGGAATATCCCCTACCTCCATATCCTCAATGGAAGATGATAGTGACAGTAGTCCTAGTCGGAGGCAGCGACTGGAGGAGGCGAAGCAGCAGAGGAAAGCGAGGCATCGCTCCCATGGCCCTCTCCTACCCACCATCGAGGATTCATCAGAAGAAGACGAATTGAGAGAGGAAGAAGAACTCCTAAGGGAGCAGGAAAAGATGAGAGAAGTCGAGCAACAGAGAATACGAAGCACAGTCCGGAAAACAAAACGCGATAAAGAAGAGTTAAGAGCACAAAGACGAAGAGAACGATCGAAGACTCCACCTAGTAATCTATCACCCATCGAGGATGCTTCTCCGACCGAGGAGTTGAGGCAGGCAGCTGAGATGGAGGAACTCCACCGGTCCTCCTGTTCAGAGTATTCTCCTTCAGCTGACTCAGATGCTGAGGGCTATGAAATTTCAACCAAGCTGTACAAATCTGGTAGTGAGTACAACCTGCCCACCTTTATGT[C/A]ACTTTATTCTCCTACTGAAAAGCCAGAAACTACATCATCTACTGCTGCTGTAACTACCTCCTCGAGTGGCAAGAAATTAAAAAGCGCAGAAGAAGTCTACGAGGAGATGATGAGGAAAGCGGAGATGTTGCAGAAGCAGCAAAAGCAGCAGACACAGCAGCAATCAAGCTCAAGTTTGATTTTACAGCAGTACAGCTCTGCCACCTATCAAGAGTCAGACATTAGAAATAGACAAGATATTGAAGATGAATATGATTATAATGAGCAAGATGATATGCATTACGAGAATGAGGAGACGGTTGATATTTATGAAGAGATCCGTCAGACCTCACAAAACATCTCAAAGCAGCTCGATGACCAAATGGAGATGGATGTTTCCTACAATGAAAAGCAGTTACTAGATACAGGCTCAGCTTTTGCTAAGTTGCTGGAACAAAGCAATGCTTTACTGACTCCTGGAACAAGCCCCACCCAGCTCTCAGCACCTGTATCGTTTTCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8919
Status:
Mutation detected in F1 DNA
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
ENSDART00000111967 Nonsense 1222 3782 8 18
ENSDART00000114444 Nonsense 1166 3719 9 19
ENSDART00000122421 Nonsense 1151 3727 9 19
Genomic Location (Zv9):
Chromosome 8 (position 55811763)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53955939
GRCz11 8 53798845
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGAAAAGCAGTTACKAGATACAGGCTCAGCYTTTGCTAAGTTGCTGGAA[C/T]AAAGCAATGCTTTACTGACTCCTGGAACAAGCCCCACCCAGCTCTCAGCA
Long Flanking Sequence:
AGGGCTATGAAATTTCAACCAAGCTGTACAAATCTGGTAGTGAGTACAACCTGCCCACCTTTATGTCACTTTATTCTCCTACTGAAAAGCCAGAAACTACATCATCTACTGCTGCTGTAACTACCTCCTCGAGTGGCAAGAAATTAAAAAGCGCAGAAGAAGTCTACGAGGAGATGATGAGGAAAGCGGAGATGTTGCAGAAGCAGCAAAAGCAGCAGACACAGCAGCAATCAAGCTCAAGTTTGATTTTACAGCAGTACAGCTCTGCCACCTATCAAGAGTCAGACATTAGAAATAGACAAGATATTGAAGATGAATATGATTATAATGAGCAAGATGATATGCATTACGAGAATGAGGAGACGGTTGATATTTATGAAGAGATCCGTCAGACCTCACAAAACATCTCAAAGCAGCTCGATGACCAAATGGAGATGGATGTTTCCTACAATGAAAAGCAGTTACTAGATACAGGCTCAGCTTTTGCTAAGTTGCTGGAA[C/T]AAAGCAATGCTTTACTGACTCCTGGAACAAGCCCCACCCAGCTCTCAGCACCTGTATCGTTTTCTGAAACCGGGACAGGAGGACGGATACCCGATGTCAGAGTGACTCAACATTTCTCAAAAGATGGCCCCAAAGACAGACTTAGAAATCAAACTGGTAAAAATGGAATTACACCAACGGTTGCTGCCACGACTATTGCTGCGTATGGAGTATATGCCAGGGAAACGGTCACTGTCTCTCAAACTACTGCCAGTCAAACAATATCCACTACACAGCCCAGTTTATATGGTCGGCAAACCACCACAACCACTACTGTTTCAAACGTGTCTCATAAAATTGCTGCAATCACTCAGGCTTACAACCAGAGGGAAAGTGCGGCACGGAAAATGGCAATAAGCAGAGGAGTGCAGATGAGGGATAGTTCAACATCCTCAGACACTAGAATTGAATCTGGCCCAAGTTCAATCAGGTCTTATGCTTACCATGAAAGGAGCCCACCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11540
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 1458 3782 8 18
ENSDART00000114444 Nonsense 1402 3719 9 19
ENSDART00000122421 Nonsense 1387 3727 9 19
Genomic Location (Zv9):
Chromosome 8 (position 55811053)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53956649
GRCz11 8 53798135
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGTTGTTACACCAGGYCTTTTTAGGCAGCAGTCCACTCAAGAYACCTA[T/G]TATAYGATTAGAACAGAGGAGCCTGAGCYCACAAGTCCATCCAAACCAGT
Long Flanking Sequence:
GTATATGCCAGGGAAACGGTCACTGTCTCTCAAACTACTGCCAGTCAAACAATATCCACTACACAGCCCAGTTTATATGGTCGGCAAACCACCACAACCACTACTGTTTCAAACGTGTCTCATAAAATTGCTGCAATCACTCAGGCTTACAACCAGAGGGAAAGTGCGGCACGGAAAATGGCAATAAGCAGAGGAGTGCAGATGAGGGATAGTTCAACATCCTCAGACACTAGAATTGAATCTGGCCCAAGTTCAATCAGGTCTTATGCTTACCATGAAAGGAGCCCACCCCTTTCTCCAACCTCATCTCCTACACACAGTCCAACACGATCTCCTTCTAGGAGAACAGCTGAGTTTTCAACACAGACAGTTAGCCCTTCAGTGTTAGCTTCCTCTGGGAACGCTTCTCACACCTCTCCAGTTATGGCACAGGGCACTCAGACCTCACATGGAGTTGTTACACCAGGTCTTTTTAGGCAGCAGTCCACTCAAGATACCTA[T/G]TATATGATTAGAACAGAGGAGCCTGAGCCCACAAGTCCATCCAAACCAGTTACAGTTAACACGGCTACATCTCCGTTGTCTTCGCCGACAAGGTTTAGCCGCCAGTCAACATTTGATGCCTACTCACCTCCTTTCAGCCCTCCTGATACACCACCACATGAACAGTCTCCTCAGCATAGCTTATACAGGAACTATAGAGCTAAAAAAGTTAATGTTGGAACTAGCATGGCCACTACTGCGAGCATGTACTCACGTGGATCAATGTCAATGGAAAACATATCACTTTGTCGCATTTCAACGGTTCCTGGTACTTCAAGAATAGAGCAAGGACATCGATTTCAAAGTGCAAGTGTAGTAGATCTACGAACTGGCATAAAGCCAACACCAATTATCATGACTGACCAAGGAATGGATTTGACATCCTTAGCGACAGAATCTCGAAAATATTCTGGGTCCCTTGAAGGAAGTCCCATTCGTCAATCCACAACTATTCAGCCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9997
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 1849 3782 9 18
ENSDART00000114444 Nonsense 1793 3719 10 19
ENSDART00000122421 Nonsense 1778 3727 10 19
Genomic Location (Zv9):
Chromosome 8 (position 55809776)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53957926
GRCz11 8 53796858
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTCCATTCTCTCAGAAACCAGTCACAGATGAGCCTTCCAAGCAATCAT[C/A]AATAGCACCGAYCACATTACCACARCATTATCAGCAGTTTGATTTACGAC
Long Flanking Sequence:
GCAAAAGCTTCAGCAACAACAACAACTTCTTGAGCAACAGCTTCAGCAACATCATCAGCTTCAGCAACAACAAGCTGCCTCTTTTGCCAATCTGAATATATCTAGCCAACTACCTCTATTCAAAAAAGACATGCTAGTCACTCAGACGAGTACTGCCACAGAAGTTAATGTCATCTCACCAGCTATGGCTTCTGATGTGTATGGTGTTGGTGGTCCTCTTGAGTTTAGGGCAAAACAAGCCGAGGCAGGTGTCATGAATCTAGCAAATGTCAAGCCTCAAGTGATGATGGTGCAAATTGATGGTGCTGCACAAGGAGCTACGATCACACAACTCGTCAAGCCTGACGAAGGCCAGGATTCAATGAATTTAACAGGGCAAATAAAATCAGAAAACCAAGCGACTTGTTGTGACATGGTTTACAATCTTCCTTTTGGTGGCAGCTGTGTGGGTGGTCCATTCTCTCAGAAACCAGTCACAGATGAGCCTTCCAAGCAATCAT[C/A]AATAGCACCGACCACATTACCACAACATTATCAGCAGTTTGATTTACGACAAGATGGGCAGACTTACCAAGATTACACAGTTAAATCTTACACATTGCCCCTCCCTGGGCGGCTTCAGCCATCAATGTCTGAAACTAACCTTTCAGAGGCAGGGTTGTCATCATATTCAGCAAAGCATGATCCACATTTTCATTCCTCTGGAGAATTATACACAGACACCATGAAGGATGGCTATGACGGAGGCTACCTTGGAATGGGGCTTCAGTATGGTTCTTTCACTGACCTTCGTCAGGGTGATATTGGAGATTTACCAATTAGAAGGTATAGCTCCCTGACCAACATTAACTCAGATTATGGATATTTCTCAAGTGATTTTGCAGAGTCTAATCTTGCCCAGTACAGTGCTACAACTGCCAGGGAGATAAGTCGCATGTGTGCAGCCCTTAACTCAATAGATAGATACAGTAGTAACCCTGATATACTACAGCTAGGCACTGGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34527
Status:
Mutation detected in F1 DNA
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
ENSDART00000111967 Nonsense 1857 3782 9 18
ENSDART00000114444 Nonsense 1801 3719 10 19
ENSDART00000122421 Nonsense 1786 3727 10 19
Genomic Location (Zv9):
Chromosome 8 (position 55809753)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53957949
GRCz11 8 53796835
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACAGATGAGCCTTCCAAGCAATCATCAATAGCACCGACCACATTACCA[C/T]AACATTATCAGCAGTTTGATTTACGACAAGATGGGCAGACTTACCAAGAT
Long Flanking Sequence:
AACTTCTTGAGCAACAGCTTCAGCAACATCATCAGCTTCAGCAACAACAAGCTGCCTCTTTTGCCAATCTGAATATATCTAGCCAACTACCTCTATTCAAAAAAGACATGCTAGTCACTCAGACGAGTACTGCCACAGAAGTTAATGTCATCTCACCAGCTATGGCTTCTGATGTGTATGGTGTTGGTGGTCCTCTTGAGTTTAGGGCAAAACAAGCCGAGGCAGGTGTCATGAATCTAGCAAATGTCAAGCCTCAAGTGATGATGGTGCAAATTGATGGTGCTGCACAAGGAGCTACGATCACACAACTCGTCAAGCCTGACGAAGGCCAGGATTCAATGAATTTAACAGGGCAAATAAAATCAGAAAACCAAGCGACTTGTTGTGACATGGTTTACAATCTTCCTTTTGGTGGCAGCTGTGTGGGTGGTCCATTCTCTCAGAAACCAGTCACAGATGAGCCTTCCAAGCAATCATCAATAGCACCGACCACATTACCA[C/T]AACATTATCAGCAGTTTGATTTACGACAAGATGGGCAGACTTACCAAGATTACACAGTTAAATCTTACACATTGCCCCTCCCTGGGCGGCTTCAGCCATCAATGTCTGAAACTAACCTTTCAGAGGCAGGGTTGTCATCATATTCAGCAAAGCATGATCCACATTTTCATTCCTCTGGAGAATTATACACAGACACCATGAAGGATGGCTATGACGGAGGCTACCTTGGAATGGGGCTTCAGTATGGTTCTTTCACTGACCTTCGTCAGGGTGATATTGGAGATTTACCAATTAGAAGGTATAGCTCCCTGACCAACATTAACTCAGATTATGGATATTTCTCAAGTGATTTTGCAGAGTCTAATCTTGCCCAGTACAGTGCTACAACTGCCAGGGAGATAAGTCGCATGTGTGCAGCCCTTAACTCAATAGATAGATACAGTAGTAACCCTGATATACTACAGCTAGGCACTGGAAGAAGCAGTGGTCCACCAAGTAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21404
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 1859 3782 9 18
ENSDART00000114444 Nonsense 1803 3719 10 19
ENSDART00000122421 Nonsense 1788 3727 10 19
Genomic Location (Zv9):
Chromosome 8 (position 55809745)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53957957
GRCz11 8 53796827
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCCTTCCAAGCAATCATCAATAGCACCGACCACATTACCACAACATTA[T/A]CAGCAGTTTGATTTACGACAAGATGGGCAGACTTACCAAGATTACACAGT
Long Flanking Sequence:
GAGCAACAGCTTCAGCAACATCATCAGCTTCAGCAACAACAAGCTGCCTCTTTTGCCAATCTGAATATATCTAGCCAACTACCTCTATTCAAAAAAGACATGCTAGTCACTCAGACGAGTACTGCCACAGAAGTTAATGTCATCTCACCAGCTATGGCTTCTGATGTGTATGGTGTTGGTGGTCCTCTTGAGTTTAGGGCAAAACAAGCCGAGGCAGGTGTCATGAATCTAGCAAATGTCAAGCCTCAAGTGATGATGGTGCAAATTGATGGTGCTGCACAAGGAGCTACGATCACACAACTCGTCAAGCCTGACGAAGGCCAGGATTCAATGAATTTAACAGGGCAAATAAAATCAGAAAACCAAGCGACTTGTTGTGACATGGTTTACAATCTTCCTTTTGGTGGCAGCTGTGTGGGTGGTCCATTCTCTCAGAAACCAGTCACAGATGAGCCTTCCAAGCAATCATCAATAGCACCGACCACATTACCACAACATTA[T/A]CAGCAGTTTGATTTACGACAAGATGGGCAGACTTACCAAGATTACACAGTTAAATCTTACACATTGCCCCTCCCTGGGCGGCTTCAGCCATCAATGTCTGAAACTAACCTTTCAGAGGCAGGGTTGTCATCATATTCAGCAAAGCATGATCCACATTTTCATTCCTCTGGAGAATTATACACAGACACCATGAAGGATGGCTATGACGGAGGCTACCTTGGAATGGGGCTTCAGTATGGTTCTTTCACTGACCTTCGTCAGGGTGATATTGGAGATTTACCAATTAGAAGGTATAGCTCCCTGACCAACATTAACTCAGATTATGGATATTTCTCAAGTGATTTTGCAGAGTCTAATCTTGCCCAGTACAGTGCTACAACTGCCAGGGAGATAAGTCGCATGTGTGCAGCCCTTAACTCAATAGATAGATACAGTAGTAACCCTGATATACTACAGCTAGGCACTGGAAGAAGCAGTGGTCCACCAAGTAGGGTTAATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45341
Status:
Mutation detected in F1 DNA
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
ENSDART00000111967 Nonsense 2092 3782 9 18
ENSDART00000114444 Nonsense 2036 3719 10 19
ENSDART00000122421 Nonsense 2021 3727 10 19
Genomic Location (Zv9):
Chromosome 8 (position 55809048)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53958654
GRCz11 8 53796130
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATTCGACTATAAACACACCTATTGCATCCACAGTTCCAATAACAACT[C/T]AGCCTTCTTCTGTGCTAAGGCCTCTGTTAAGAGGAGGATACAGACCATAT
Long Flanking Sequence:
ATGGCTATGACGGAGGCTACCTTGGAATGGGGCTTCAGTATGGTTCTTTCACTGACCTTCGTCAGGGTGATATTGGAGATTTACCAATTAGAAGGTATAGCTCCCTGACCAACATTAACTCAGATTATGGATATTTCTCAAGTGATTTTGCAGAGTCTAATCTTGCCCAGTACAGTGCTACAACTGCCAGGGAGATAAGTCGCATGTGTGCAGCCCTTAACTCAATAGATAGATACAGTAGTAACCCTGATATACTACAGCTAGGCACTGGAAGAAGCAGTGGTCCACCAAGTAGGGTTAATCTTCCTCAAGGTCCCAGACTTGGTTTTAAGTACAGCCCAGATAGAAAGCCCCTTTCCCATAGTCAAGCTCTAACTGATCTGATCAATGCAAGACAAGCTAGTCTTCGAGCCATGTATCCATCAGCTATTAGATCAGCGGATGGCATGATATATTCGACTATAAACACACCTATTGCATCCACAGTTCCAATAACAACT[C/T]AGCCTTCTTCTGTGCTAAGGCCTCTGTTAAGAGGAGGATACAGACCATATCCTACACCGAATATGACACCTGTACCTTTGGCAAGCTTAACCAGATTGCCAGTAGCTCCAAGGACTGGGCAGGCACCTTTCCAATGTCCTACACCTAATCCTCTCCCTGTTACAACATCTACAAAAGTACCCGAGTCTCCAGCTATCACAACAGTCCAAGATGCACCATTGTATCTTGGCAAGTCTCCAGTTAGCATAACAGCAGCTGGAACTTTTGCGCAGCCAATTCAGCCCTCTTCTGTGCCTATTTCAACACCAATGAACTTGGCAATGAGCCAACCTGAGGTCCAAGCTCAACCAATAAATCTATCTCAGTCCCATCTTCAGGCGAATACCCAACCTACTTTACAACATCAACTACCACAATCTAACTCATCTGCTCAATCACACCCTCCAGTGCAAGGTCACCCGATTGCAACTCAAGGAGGTCGGACTACTCTTACTGCTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21403
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 2280 3782 10 18
ENSDART00000114444 Nonsense 2224 3719 11 19
ENSDART00000122421 Nonsense 2209 3727 11 19
Genomic Location (Zv9):
Chromosome 8 (position 55808442)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53959260
GRCz11 8 53795524
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACTTTTGCAAATTGAGAGAGAGAGAGTGGAACTGGAAAAGTTGCGT[C/T]AGCTAAGGCTTCAGGAAGAGCTTGAGCGTGAGCGTGCAGAGTTGCAGAGG
Long Flanking Sequence:
CTCCAAGGACTGGGCAGGCACCTTTCCAATGTCCTACACCTAATCCTCTCCCTGTTACAACATCTACAAAAGTACCCGAGTCTCCAGCTATCACAACAGTCCAAGATGCACCATTGTATCTTGGCAAGTCTCCAGTTAGCATAACAGCAGCTGGAACTTTTGCGCAGCCAATTCAGCCCTCTTCTGTGCCTATTTCAACACCAATGAACTTGGCAATGAGCCAACCTGAGGTCCAAGCTCAACCAATAAATCTATCTCAGTCCCATCTTCAGGCGAATACCCAACCTACTTTACAACATCAACTACCACAATCTAACTCATCTGCTCAATCACACCCTCCAGTGCAAGGTCACCCGATTGCAACTCAAGGAGGTCGGACTACTCTTACTGCTGTTAGAAATATCGCAAGTCAAGAAAACGAAACTGAGGAAAAAGTCCATCAACAGCAGGAACAACTTTTGCAAATTGAGAGAGAGAGAGTGGAACTGGAAAAGTTGCGT[C/T]AGCTAAGGCTTCAGGAAGAGCTTGAGCGTGAGCGTGCAGAGTTGCAGAGGCATAGAGAAAAGGAGCAGATACTTGTACAGCGTGAGATTCAGGAACTGCAGAGTATAAAGCAACAAGTGTTGCAGCAGCAGCAAGCTGAGAGAGAAAGCCAGCTGATTCTACAGAGAGAGCAACTAGCTCAACAGAAACAGCAGCTTGATCAGATACAATCTTTGCAACATCAGTTGCAGCAGCAACTTGAGGAACAAAAGAGACAAAAGACAGTCAGTGGAAGCACCCAAGTCATCAGTGATCAATCTGGAAGAATTATTCAGCCACAGGAATTAGCCTCCGATGTATTATATAATGACGTTCAGGTTTTTGTTAGATCAATGCCAAATTCCACATCAGAAATATGCTTGAGAAGTACTGAAGATCAGGCAGAAATTAGGTCCATGCGTAAACAAAGATCTATGCCAAGATTGCAAGATGGAAATGAGGGTGAAGTGACGATGTTCCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2454
Status:
F2 line generated
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
ENSDART00000111967 Nonsense 2354 3782 10 18
ENSDART00000114444 Nonsense 2298 3719 11 19
ENSDART00000122421 Nonsense 2283 3727 11 19
ENSDART00000111967 Nonsense 2354 3782 10 18
ENSDART00000114444 Nonsense 2298 3719 11 19
ENSDART00000122421 Nonsense 2283 3727 11 19
Genomic Location (Zv9):
Chromosome 8 (position 55808220)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53959482
GRCz11 8 53795302
KASP Assay ID:
554-3184.1 (used for ordering genotyping assays)
KASP Sequence:
AAYTAGCTCAACAGAAACAGCAGCTTGATCAGATACAATCTTTGCAACAT[C/T]AGTTGCAGCAGCAACTTGAGGAACAAAAGANNNNNNNNNCAGTCAGTGGA
Long Flanking Sequence:
AACCTGAGGTCCAAGCTCAACCAATAAATCTATCTCAGTCCCATCTTCAGGCGAATACCCAACCTACTTTACAACATCAACTACCACAATCTAACTCATCTGCTCAATCACACCCTCCAGTGCAAGGTCACCCGATTGCAACTCAAGGAGGTCGGACTACTCTTACTGCTGTTAGAAATATCGCAAGTCAAGAAAACGAAACTGAGGAAAAAGTCCATCAACAGCAGGAACAACTTTTGCAAATTGAGAGAGAGAGAGTGGAACTGGAAAAGTTGCGTCAGCTAAGGCTTCAGGAAGAGCTTGAGCGTGAGCGTGCAGAGTTGCAGAGGCATAGAGAAAAGGAGCAGATACTTGTACAGCGTGAGATTCAGGAACTGCAGAGTATAAAGCAACAAGTGTTGCAGCAGCAGCAAGCTGAGAGAGAAAGCCAGCTGATTCTACAGAGAGAGCAACTAGCTCAACAGAAACAGCAGCTTGATCAGATACAATCTTTGCAACAT[C/T]AGTTGCAGCAGCAACTTGAGGAACAAAAGAGACAAAAGACAGTCAGTGGAAGCACCCAAGTCATCAGTGATCAATCTGGAAGAATTATTCAGCCACAGGAATTAGCCTCCGATGTATTATATAATGACGTTCAGGTTTTTGTTAGATCAATGCCAAATTCCACATCAGAAATATGCTTGAGAAGTACTGAAGATCAGGCAGAAATTAGGTCCATGCGTAAACAAAGATCTATGCCAAGATTGCAAGATGGAAATGAGGGTGAAGTGACGATGTTCCCTTTGCCTCAGAGGCTTGTGGACTGCAGTGTGCAAACAGATGATGAAGATGGAGAGGAGAGATACCTAGTATCAAGAAGACGACGGACTAGGCGTAGTGTTGACTGCAGCGTTCAGACAGATGATGACGAAGACAAGGCAGAATGGGAGCAGCCAGTTAGACGTAGACGTTCCCGTTACTCAAGGCATTCTGCTGAATCTAACACAGACCATAAATCTGAATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7284
Status:
Mutation detected in F1 DNA
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
ENSDART00000111967 Nonsense 2354 3782 10 18
ENSDART00000114444 Nonsense 2298 3719 11 19
ENSDART00000122421 Nonsense 2283 3727 11 19
ENSDART00000111967 Nonsense 2354 3782 10 18
ENSDART00000114444 Nonsense 2298 3719 11 19
ENSDART00000122421 Nonsense 2283 3727 11 19
Genomic Location (Zv9):
Chromosome 8 (position 55808220)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53959482
GRCz11 8 53795302
KASP Assay ID:
554-3184.1 (used for ordering genotyping assays)
KASP Sequence:
AAYTAGCTCAACAGAAACAGCAGCTTGATCAGATACAATCTTTGCAACAT[C/T]AGTTGCAGCAGCAACTTGAGGAACAAAAGANNNNNNNNNCAGTCAGTGGA
Long Flanking Sequence:
AACCTGAGGTCCAAGCTCAACCAATAAATCTATCTCAGTCCCATCTTCAGGCGAATACCCAACCTACTTTACAACATCAACTACCACAATCTAACTCATCTGCTCAATCACACCCTCCAGTGCAAGGTCACCCGATTGCAACTCAAGGAGGTCGGACTACTCTTACTGCTGTTAGAAATATCGCAAGTCAAGAAAACGAAACTGAGGAAAAAGTCCATCAACAGCAGGAACAACTTTTGCAAATTGAGAGAGAGAGAGTGGAACTGGAAAAGTTGCGTCAGCTAAGGCTTCAGGAAGAGCTTGAGCGTGAGCGTGCAGAGTTGCAGAGGCATAGAGAAAAGGAGCAGATACTTGTACAGCGTGAGATTCAGGAACTGCAGAGTATAAAGCAACAAGTGTTGCAGCAGCAGCAAGCTGAGAGAGAAAGCCAGCTGATTCTACAGAGAGAGCAACTAGCTCAACAGAAACAGCAGCTTGATCAGATACAATCTTTGCAACAT[C/T]AGTTGCAGCAGCAACTTGAGGAACAAAAGAGACAAAAGACAGTCAGTGGAAGCACCCAAGTCATCAGTGATCAATCTGGAAGAATTATTCAGCCACAGGAATTAGCCTCCGATGTATTATATAATGACGTTCAGGTTTTTGTTAGATCAATGCCAAATTCCACATCAGAAATATGCTTGAGAAGTACTGAAGATCAGGCAGAAATTAGGTCCATGCGTAAACAAAGATCTATGCCAAGATTGCAAGATGGAAATGAGGGTGAAGTGACGATGTTCCCTTTGCCTCAGAGGCTTGTGGACTGCAGTGTGCAAACAGATGATGAAGATGGAGAGGAGAGATACCTAGTATCAAGAAGACGACGGACTAGGCGTAGTGTTGACTGCAGCGTTCAGACAGATGATGACGAAGACAAGGCAGAATGGGAGCAGCCAGTTAGACGTAGACGTTCCCGTTACTCAAGGCATTCTGCTGAATCTAACACAGACCATAAATCTGAATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21402
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 2629 3782 10 18
ENSDART00000114444 Nonsense 2573 3719 11 19
ENSDART00000122421 Nonsense 2558 3727 11 19
Genomic Location (Zv9):
Chromosome 8 (position 55807395)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53960307
GRCz11 8 53794477
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACCGGTGTCCATTTAGTTGGTTCTGCAGATCCACTCTCACCAAGTCAT[C/T]AGAATGCCGTGAAGTTTGGAAGGCGGAGGCCCGATCCTTTGGAGTTTGGC
Long Flanking Sequence:
ATGGAGAGGAGAGATACCTAGTATCAAGAAGACGACGGACTAGGCGTAGTGTTGACTGCAGCGTTCAGACAGATGATGACGAAGACAAGGCAGAATGGGAGCAGCCAGTTAGACGTAGACGTTCCCGTTACTCAAGGCATTCTGCTGAATCTAACACAGACCATAAATCTGAATCACATTTTACACCTTCATCTGTTAAGACAGCATCCTCCAGTATTGCCATACAGACCATTCGAGATTGTTCTTGCCAAACAGAGACAGAGCAGCTGGTTAGAGTATCCCCAAGCATACATGCCACCATACCAGATCCTAGCAAGGTTGAAATTGTCCACTATATTTCTGGTCCTGAGAGAACACAGAAGGGTCAAAGTTTAGCTTGCCAAACTGAACCTGAGACTCAGTCTCAAAGCATAGTCATTCCACAGATAAGCATCGCTACCACGGTCAGCCCCACCGGTGTCCATTTAGTTGGTTCTGCAGATCCACTCTCACCAAGTCAT[C/T]AGAATGCCGTGAAGTTTGGAAGGCGGAGGCCCGATCCTTTGGAGTTTGGCTACCAGCAGCATCACCTGCATAACGAGTCTCTATCCAGCTTGATCCGGCAACAACCTAAATCTCCACAGGTGCTGTATTCCCCTGTTTCTCCTCTTTCTTCTCCACAACGCATCATAGACACATCATTCTCTTCTAGTGAGAGGCTGAATAAAGCACATGTCACCCCGCAGCAGAAATCCTGTATTGCCGAGCCATCCCAGAGACATCAGGCCATTCCTCGTCCAATGAAGAATATCCAGAGATCTATGTCAGACCCTAAGCCACTTAGTCCCACTACAGATGAACATACCAAGGCTAGGATTTCACTTTATCAACAGCAAGCCCTTCAGAGTCAGGTATGGGTAATTCATTTTTTGATTCTTAACTTGCACTTGCTTTGCACAAAGGACAAACTGAACTTGTGAATAATACAACAGTAGTGGAGCTTTATTTATGTTGTTTGTGTGTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25413
Status:
Mutation detected in F1 DNA
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
ENSDART00000111967 Essential Splice Site 2757 3782 None 18
ENSDART00000114444 Essential Splice Site 2701 3719 None 19
ENSDART00000122421 Essential Splice Site 2686 3727 None 19
Genomic Location (Zv9):
Chromosome 8 (position 55807007)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53960695
GRCz11 8 53794089
KASP Assay ID:
554-7700.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCAAGGCTAGGATTTCACTTTATCAACAGCAAGCCCTTCAGAGTCAGG[T/A]ATGGGTAATTCATTTTTTGATTCTTAACTTGCACTTGCTTTGCACAAAGG
Long Flanking Sequence:
ACCTGAGACTCAGTCTCAAAGCATAGTCATTCCACAGATAAGCATCGCTACCACGGTCAGCCCCACCGGTGTCCATTTAGTTGGTTCTGCAGATCCACTCTCACCAAGTCATCAGAATGCCGTGAAGTTTGGAAGGCGGAGGCCCGATCCTTTGGAGTTTGGCTACCAGCAGCATCACCTGCATAACGAGTCTCTATCCAGCTTGATCCGGCAACAACCTAAATCTCCACAGGTGCTGTATTCCCCTGTTTCTCCTCTTTCTTCTCCACAACGCATCATAGACACATCATTCTCTTCTAGTGAGAGGCTGAATAAAGCACATGTCACCCCGCAGCAGAAATCCTGTATTGCCGAGCCATCCCAGAGACATCAGGCCATTCCTCGTCCAATGAAGAATATCCAGAGATCTATGTCAGACCCTAAGCCACTTAGTCCCACTACAGATGAACATACCAAGGCTAGGATTTCACTTTATCAACAGCAAGCCCTTCAGAGTCAGG[T/A]ATGGGTAATTCATTTTTTGATTCTTAACTTGCACTTGCTTTGCACAAAGGACAAACTGAACTTGTGAATAATACAACAGTAGTGGAGCTTTATTTATGTTGTTTGTGTGTACCATAAAATTTAATTACTGATGCTGTCTTTCTGGAGTTTGAAGTTGCAATGTGATGTGAATTACAAGGGCTGCAAATATGAGATGCTAAAATTTGTTTGTCCCTTGAACTTTCTGGTTTAGTGTTTCAATTTAGTTTGTCGGTGTTTTTTTTTTGTTTATTGTTGTGTTCTGCTAAGATCAGGTACAGTATTCAGAATGTCTGTTCAAAATGTGCACATTTTTGCATTCATGACTTAATTAAATCAACCTTATATTAGTTTTTCTCACTTTTTGTCTGCTTGAATGTTTCCTCTTGGTCTTGAGATAAACTCTGCGTTCTTAATTGTTACAGCAGAAACACATTGTATTGCTGTAAATAGGACCAAACAGAAAACTAGCATGTCTGATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7165
Status:
Mutation detected in F1 DNA
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
ENSDART00000111967 Nonsense 3043 3782 13 18
ENSDART00000114444 Nonsense 2987 3719 14 19
ENSDART00000122421 Nonsense 2986 3727 13 19
Genomic Location (Zv9):
Chromosome 8 (position 55805334)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53962368
GRCz11 8 53792416
KASP Assay ID:
554-4821.1 (used for ordering genotyping assays)
KASP Sequence:
CCAAGACAGACATCACTTGCTGACCTTGAACACAAAATGCCCACTAATTA[T/A]GAAGTTATAAGCAATCCCACAGTTGTAGTCACAACCACTGCCCAAGAAAT
Long Flanking Sequence:
ACTTGTGAGCTGAACACTGCTGCCCAGTTTCCCCCCACATCATCTTTTGTGTCGTACCAGTACCCCCAAAGTCTCCCGACGGTACCTACCCCACAGGCCTCTACATTGCAGAGCACAAGTTTCAACCAACCTCCCTATCCGTCCGTGACCCAAGCTCAAGCTCTCCCCCAGCCCACTCCCTTACAGACTTATCCAACCCTGCCCTATCAGGTCCAAGGGTCATTTCCATCCCAAGTCTTTCCACAGAGTCAGCCTCCATATCCAGCAGACACTTCCATGCCACCATCAGCACAGCCAAGCCAACCAGGGTTTCAGGCTACCTTACCGCCTACTGGTCCAGTCCCTTATCCAACCCACAATACACCATACCCAAGCCAGGCACCCCCCTATCCGGTCAGTCAAGCAAGCACTTACCAACCACAGACAGACACTCTCACTTTTCACCAAAAGCCAAGACAGACATCACTTGCTGACCTTGAACACAAAATGCCCACTAATTA[T/A]GAAGTTATAAGCAATCCCACAGTTGTAGTCACAACCACTGCCCAAGAAATCAGTTACAGCCAGTCTGGTTTGGGTCCATCTTATGGCCAATACAGCACAACCATGGCAAGCACTTATGGTCCCTACTCCTCAACTGTTTCAAATACATATGGTGGGCCTTTAACAACCTCTGCACCTTCTGGTTATGGGCCATACACAACAATCTCATCCAGTAGTTATGGGCAGTACACAACAACAACTGCAAATGCTTATGGATATACAGTAACCACGGCTAGTTCTTATGGGCAATATAATCCCGTTGTTACAAATTCATATGGCCAGACAACACTATCTGACCATATGCACTCAATGGACAGCCCCTCTATGTACGGCAGTGATGGCTTATATGGATCCTCCAACCTAGAGCAGAGTGTCCCAAGGAACTATGTTATGATCGATGACATTTGCGAACTGACCAAGGACGGCATGGGCACGAGTTCAGATTCACATCGCGGTGAGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41315
Status:
Mutation detected in F1 DNA
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
ENSDART00000111967 Nonsense 3111 3782 14 18
ENSDART00000114444 Nonsense 3056 3719 15 19
ENSDART00000122421 Nonsense 3054 3727 14 19
ENSDART00000111967 Nonsense 3111 3782 14 18
ENSDART00000114444 Nonsense 3056 3719 15 19
ENSDART00000122421 Nonsense 3054 3727 14 19
Genomic Location (Zv9):
Chromosome 8 (position 55804908)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53962794
GRCz11 8 53791990
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGGCTTATATGGATCCTCCAACCTAGAGCAGAGTGTCCCAAGGAACTA[T/A]GTTATGATCGATGACATTTGCGAACTGACCAAGGACGGCATGGGCACGAG
Long Flanking Sequence:
GACACTCTCACTTTTCACCAAAAGCCAAGACAGACATCACTTGCTGACCTTGAACACAAAATGCCCACTAATTATGAAGTTATAAGCAATCCCACAGTTGTAGTCACAACCACTGCCCAAGAAATCAGTTACAGCCAGTCTGGTTTGGGTCCATCTTATGGCCAATACAGCACAACCATGGCAAGCACTTATGGTCCCTACTCCTCAACTGTTTCAAATACATATGGTGGGCCTTTAACAACCTCTGCACCTTCTGGTTATGGGCCATACACAACAATCTCATCCAGTAGTTATGGGCAGTACACAACAACAACTGCAAATGCTTATGGATATACAGTAACCACGGCTAGTTCTTATGGGCAATATAATCCCGTTGTTACAAATTCATATGGCCAGACAACACTATCTGACCATATGCACTCAATGGACAGCCCCTCTATGTACGGCAGTGATGGCTTATATGGATCCTCCAACCTAGAGCAGAGTGTCCCAAGGAACTA[T/A]GTTATGATCGATGACATTTGCGAACTGACCAAGGACGGCATGGGCACGAGTTCAGATTCACATCGCGGTGAGGGTCACGGACGATATGGGAGTGATGGACTTCATACTCGAGGGCAGAGCTCCTTTGGAAGACCGGAGGATGAACGTGATGCAGATCTGTACGACCAGCATCATGGCAGGGGTAAGAGCACCTGCAGCTACCAAGCACAAGGGGCAAACACGCATGGCCGGGTAGTGGGAAGCAGTAGCATGGGTGGGGGATCGTCATATTACTATGATGACTGCAGTCACTCGGCACCTACGTGGGCAGCCCAGAGGCACTCCACAAAAAACCTGTGCCCTTCCGCCGTCATGTCCTCCAAGAGGAGCAAACATCGTAAACAAGGCATTGAACAGAAGATGTCCAAGTTTTCCCCAATTGAGGAAGCTCATGATGTGGAGGCTGATCTGGCCTCCTACACCATGGGTACCTCCGCAACAAGTGGTTATGGCTCAGGTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30911
Status:
Mutation detected in F1 DNA
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
ENSDART00000111967 Nonsense 3111 3782 14 18
ENSDART00000114444 Nonsense 3056 3719 15 19
ENSDART00000122421 Nonsense 3054 3727 14 19
ENSDART00000111967 Nonsense 3111 3782 14 18
ENSDART00000114444 Nonsense 3056 3719 15 19
ENSDART00000122421 Nonsense 3054 3727 14 19
Genomic Location (Zv9):
Chromosome 8 (position 55804908)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53962794
GRCz11 8 53791990
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGGCTTATATGGATCCTCCAACCTAGAGCAGAGTGTCCCAAGGAACTA[T/A]GTTATGATCGATGACATTTGCGAACTGACCAAGGACGGCATGGGCACGAG
Long Flanking Sequence:
GACACTCTCACTTTTCACCAAAAGCCAAGACAGACATCACTTGCTGACCTTGAACACAAAATGCCCACTAATTATGAAGTTATAAGCAATCCCACAGTTGTAGTCACAACCACTGCCCAAGAAATCAGTTACAGCCAGTCTGGTTTGGGTCCATCTTATGGCCAATACAGCACAACCATGGCAAGCACTTATGGTCCCTACTCCTCAACTGTTTCAAATACATATGGTGGGCCTTTAACAACCTCTGCACCTTCTGGTTATGGGCCATACACAACAATCTCATCCAGTAGTTATGGGCAGTACACAACAACAACTGCAAATGCTTATGGATATACAGTAACCACGGCTAGTTCTTATGGGCAATATAATCCCGTTGTTACAAATTCATATGGCCAGACAACACTATCTGACCATATGCACTCAATGGACAGCCCCTCTATGTACGGCAGTGATGGCTTATATGGATCCTCCAACCTAGAGCAGAGTGTCCCAAGGAACTA[T/A]GTTATGATCGATGACATTTGCGAACTGACCAAGGACGGCATGGGCACGAGTTCAGATTCACATCGCGGTGAGGGTCACGGACGATATGGGAGTGATGGACTTCATACTCGAGGGCAGAGCTCCTTTGGAAGACCGGAGGATGAACGTGATGCAGATCTGTACGACCAGCATCATGGCAGGGGTAAGAGCACCTGCAGCTACCAAGCACAAGGGGCAAACACGCATGGCCGGGTAGTGGGAAGCAGTAGCATGGGTGGGGGATCGTCATATTACTATGATGACTGCAGTCACTCGGCACCTACGTGGGCAGCCCAGAGGCACTCCACAAAAAACCTGTGCCCTTCCGCCGTCATGTCCTCCAAGAGGAGCAAACATCGTAAACAAGGCATTGAACAGAAGATGTCCAAGTTTTCCCCAATTGAGGAAGCTCATGATGTGGAGGCTGATCTGGCCTCCTACACCATGGGTACCTCCGCAACAAGTGGTTATGGCTCAGGTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34526
Status:
Mutation detected in F1 DNA
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
ENSDART00000111967 Nonsense 3209 3782 14 18
ENSDART00000114444 Nonsense 3154 3719 15 19
ENSDART00000122421 Nonsense 3152 3727 14 19
Genomic Location (Zv9):
Chromosome 8 (position 55804615)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53963087
GRCz11 8 53791697
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTAGCATGGGTGGGGGATCGTCATATTACTATGATGACTGCAGTCACT[C/A]GGCACCTACGTGGGCAGCCCAGAGGCACTCCACAAAAAACCTGTGCCCTT
Long Flanking Sequence:
TGGGCAGTACACAACAACAACTGCAAATGCTTATGGATATACAGTAACCACGGCTAGTTCTTATGGGCAATATAATCCCGTTGTTACAAATTCATATGGCCAGACAACACTATCTGACCATATGCACTCAATGGACAGCCCCTCTATGTACGGCAGTGATGGCTTATATGGATCCTCCAACCTAGAGCAGAGTGTCCCAAGGAACTATGTTATGATCGATGACATTTGCGAACTGACCAAGGACGGCATGGGCACGAGTTCAGATTCACATCGCGGTGAGGGTCACGGACGATATGGGAGTGATGGACTTCATACTCGAGGGCAGAGCTCCTTTGGAAGACCGGAGGATGAACGTGATGCAGATCTGTACGACCAGCATCATGGCAGGGGTAAGAGCACCTGCAGCTACCAAGCACAAGGGGCAAACACGCATGGCCGGGTAGTGGGAAGCAGTAGCATGGGTGGGGGATCGTCATATTACTATGATGACTGCAGTCACT[C/A]GGCACCTACGTGGGCAGCCCAGAGGCACTCCACAAAAAACCTGTGCCCTTCCGCCGTCATGTCCTCCAAGAGGAGCAAACATCGTAAACAAGGCATTGAACAGAAGATGTCCAAGTTTTCCCCAATTGAGGAAGCTCATGATGTGGAGGCTGATCTGGCCTCCTACACCATGGGTACCTCCGCAACAAGTGGTTATGGCTCAGGTTCCCAGTACTATAAACTTCAGGATGGCATCTATGCGCTACGGAGTACTTACAGTCCACAGCGGGGCTACTATAATGATGAACGTCTCTATGGCTACGGCAGGTCCCGTTCAGCTGGTTATGGCATGGACAAAATCTCTCCCTGCGAGAGGAGCTACAGAAGCAGATCATATGAACGGGACCGTGTAGACCGGTCATACCACAGCAACTATGGCCACAGTGTGCACCCCACTTTGCAATCCCAGTATTCAGACAAGGAGAACTCCCATGCCATGACAAAGCTCATGGGTGTTGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11595
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111967 Nonsense 3621 3782 15 18
ENSDART00000114444 Nonsense 3566 3719 16 19
ENSDART00000122421 Nonsense 3564 3727 15 19
Genomic Location (Zv9):
Chromosome 8 (position 55802872)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53964830
GRCz11 8 53789954
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTYAGGTTCCAGTAGGCAAGGTGTCTCCCAGCCTCCAGTTGATGGGCAG[C/T]AAGGGCAGCGAACGCAACTTCAACAGCAGGCACAGACTTCAGCAGCCAGG
Long Flanking Sequence:
GTCATTCTGGGAGACGAGGCCATGTCAAGCACACATACCATGATTATGATGAGCCACCAGAAGATCTGTGGCCGCAAGATGATTACGGTCACACCCGCCACATTTCTTCTCGTGAGCACCGTCATCATAGCAGCGGGAGTTCTGGTCGGCACTCTACACGCCACTCTGATGAGCCTCGTTCCTCTCGATCATCTCGTTCCTCAAAGGATCCGTCCATCCGGCATGACTCCCGCTCCTTGTCATCTTCAGGGAGGAGGGGAGACTCTCGTTCTCAGGGCTACCACTCCTCAGATTATTCCCGCGACACCTCAGGCCATCATCACAGCTCCCGTTCTGGAAAACAATCATCTTCCCACCATCAAGGATCATCTAGTAGGAAGCAACAGGATCATCCCTCGTCATCTAGGCAGCCAGGATCTCTTGGGGCTGGACAGAAAGGTCCTAGTGGACCTTCAGGTTCCAGTAGGCAAGGTGTCTCCCAGCCTCCAGTTGATGGGCAG[C/T]AAGGGCAGCGAACGCAACTTCAACAGCAGGCACAGACTTCAGCAGCCAGGCCCGGGTCTCAGACGTCCACCGCAGGTGCAGTGCAGCCACAGTTAGTGCAAGCCCAGCAACTGCAAGCCAAACCTGGCCAAACTGGTCCAATGCCCCGACAGCCCACCTCAGCAGCGCAGACATCCCCAGCTGCAGTAAGTGAATATATTAGCTTGATGTCATGGTTTGGTTCCTTTGGCCAATGTGAACAATGTCGTCCTAGACCCTAAACTGCAAACCGTGCCCCATAAGTAGGCCTACATATTAAGGCCTACATATTATCTTGACATATTAAGTGTTGTGAGATAAGAGTAGTATTTTAAATAATATGTATTTATTTGTCTTTTGTTTCCAGCCGATTAAACCAGAGCCCACACCTGCCACTGCTATTGGAGCAAAAGCAGTCCCCGGACAGCCTGCCAAAACAGCCCAGCCTCCACTCACCGGGATAGGTAATTATGCCATATAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44694
Status:
Mutation detected in F1 DNA
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
ENSDART00000111967 Essential Splice Site 3770 3782 18 18
ENSDART00000114444 Essential Splice Site 3707 3719 19 19
ENSDART00000122421 Essential Splice Site 3715 3727 19 19
Genomic Location (Zv9):
Chromosome 8 (position 55800962)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 53966740
GRCz11 8 53788044
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATAACAAATGTTAATCTCTCAATTTTCTCCTTTAATTTCTCTGTCGCA[G/A]CCATCTCTGGATTTGGCAAGAAGTTCACCTCGTTGTGGTGAGGTGCAGGT
Long Flanking Sequence:
TAATTAAATGATTTTGTTTTTAATGCCATGCACAGTTGAACTGTTCAGCAAAACATTAGCAAAGTGAGCTGACAGAATCAATGTGGTTAGTTTTGATTTCAGGTGTGCTTTAAAGGGACAGTACGGCTGCACAATATATAGATTCAGCATTGATATCGCAATGCGCACATCCACAATAGTATTACACAACACCAACTCAGACAATATATCACTTTAAAAATGTTCATGAAAGTGACTTTTTACAACTTTTCAAGCTCAAAAGGTGTTGGAAGAAAGATCAAGCTCCCATAATGCAATTGCAAAGCAGAAATAAACAAGGAAAAAATAAAAACATCAATCATTAAATACAGCAAACTGCTTTATAGTGTGCTTCTTGTGGCTGAGTAAAGTAACAGGACATTTTAATATTCTGGTGATCTGAATTATTTCTTAATTATATTGTTAGATTGTTTATAACAAATGTTAATCTCTCAATTTTCTCCTTTAATTTCTCTGTCGCA[G/A]CCATCTCTGGATTTGGCAAGAAGTTCACCTCGTTGTGGTGAGGTGCAGGTAAAGGTGAGTGCAGTTTTTCATGCCATGCTTTAATGTCCAATTATGTAACTGCAGTATAGAAAATATGTGGGAACACTTTACAATTAGGTGTCATTACTCAATGTTAGTTATTGTTAGTTAACACTAGTACCACATTTATTAATAATGGTTAACCATTTAATAATGCATTGTAAACATTCAAATTCATGCATTTACACTCACTGGCCACTTTATTAGGTACACCATACTAGTGCCTTTAGAACTGCTTTAATCCTTGGTGTCAGAGATTCAACAAGCTACTGGAAATATTCCTCAGAGATTTTGCTCCATATTGTCATGATAGCATCACACAGTTGCTGCAGATTTGTCGGCTGCACATCCATGATGCCAATCTCCCGTTCCACCACATCCCAAAGCTGCTCTATTGGATTGAGCTCTGGTGACTGTGGAGGCCATTTGAGTACAGTGAA
Associated Phenotype:
Not determined