ZMP
CACNA1H (1 of 3)
Ensembl ID:
Description:
calcium channel, voltage-dependent, T type, alpha 1H subunit [Source:HGNC Symbol;Acc:1395]
Human Orthologue:
CACNA1H
Human Description:
calcium channel, voltage-dependent, T type, alpha 1H subunit [Source:HGNC Symbol;Acc:1395]
Mouse Orthologue:
Cacna1h
Mouse Description:
calcium channel, voltage-dependent, T type, alpha 1H subunit Gene [Source:MGI Symbol;Acc:MGI:1928842
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20094 | Nonsense | Available for shipment | Available now |
sa16069 | Essential Splice Site | Available for shipment | Available now |
sa16182 | Essential Splice Site | Available for shipment | Available now |
sa33266 | Nonsense | Available for shipment | Available now |
sa17053 | Nonsense | Available for shipment | Available now |
sa17795 | Essential Splice Site | Available for shipment | Available now |
sa10926 | Essential Splice Site | Available for shipment | Available now |
sa13577 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20094
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 |
---|---|---|---|---|---|
ENSDART00000085210 | Nonsense | 556 | 2114 | 8 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 39874013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 39737373 |
GRCz11 | 3 | 39879231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAAATACAGGACATGAGGTGATACAGGACTTTGACAAGCTGCACCAG[C/T]AAATTGAAGCACATAGTAAGTTTTTTTTTTTTTAATTGCCGTTGTTTGGC
Long Flanking Sequence:
GGCGAAAGAAAGTGAACCCCAACACCGGGGCTGGCGGAGGTGCCAATGGTCACAGTAGGCACAGGGGTTACGGACACTGGGTACAGTCCATTCACAGCCTCATCCAGCAGCACCAGCGACAGCACTGTCACCTCAGCAATGGCAGCCCCAGTCCTGTGGCCACTACGGGCTCCAGTGAGGCTCTGGAAATGAGGTCCATCACAGCGGGTCAGCAGCTGACCGTGTCCTCTCAGCCAACCGCCACGCACAATCTTTCTTCCAGCACACAATCAGTGCATAGCATTTATCAAGGTGACTTTCGTGAGGCCCCGCAGGAGCGAACACCCACTAATGTTGCTGTTCCGGCACTCAGCCGACTCAATGGGGGGATGAACTATCCCACAATTTTGCCGTCCCTCATTTGCAACTATTCAGGTGGAGGTTCATTAGGGAAAGAGAGGGGGAAGTCGGATGCAAATACAGGACATGAGGTGATACAGGACTTTGACAAGCTGCACCAG[C/T]AAATTGAAGCACATAGTAAGTTTTTTTTTTTTTAATTGCCGTTGTTTGGCCTTCTCATCAGGTTCAGTAGTCACCTCACACAGCCTGTTTCAGGAAAATGAAATGCTTTCTGAAAAGTGATTGTTAGGCAGCTCTTATGGATGTGACAGTAAATCGATACTTCAAATGTTAAAGTCATTAACGCAATCTTTAAAGGAGTGAGGCAACAGCGAGCGACCACGGCTGTCAGGGCTTTCGAAATTCTACAGCAGCAGTTGATACATCATGTTAGATGGATAGGCTGGAGGCTTAATCTGTCATTGGAGGGAAAAGATCAGTTGGTTGTAAATGATTTAGTCTTTTGAGGTTTCTAGGCCTGGCTGTAGAGTTAGGTCAATCAAACACTATACAGTGTCTTTTTAAACACCCAAAATTACAAGAAACTCTGGAGGAATTGTGAATAGCATTATGACGCAATGACGCTAATCAATCTATGATATGAAAAATTATATCATTGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16069
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 |
---|---|---|---|---|---|
ENSDART00000085210 | Essential Splice Site | 690 | 2114 | 11 | 36 |
ENSDART00000085210 | Essential Splice Site | 690 | 2114 | 11 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 39902235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 39765595 |
GRCz11 | 3 | 39907453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCTGTGGTCTGCAGAAGGTAATGAGGTGTGGCTGTGTTTCCYTTCACA[G/A]CCCGAGGAGCTGACMAACATCCTGGAGATCAGCAACATCGTCTTCACTAG
Long Flanking Sequence:
GTAATTCTTCACTCTCAAGAGCTGAAGCGCTGTCTGCATCAGCAAATGCAAGAAGACCAATTCTCTGGCCCCGAAACTGCTTATGATGGACAGATTCTACAAGCTCTGTCCGTCTGATTGATCTGCGTTGCTCTGCTCTTAATAAAGGAGCTTATTATGCTTTAGGTTTGCTTTTGCTTATCCAAGCTCAGCAGCAGAGCCGTTTGTGTTGAAGCTGAACAATTGTAATTGCTTGGTAAGTGTGCTGACGGTTTGGCCCAGAGGTAATGCGTTACGTAAACTGTCCATTTATCATCTGAATGTGCTGAATGGTTTTGCGTATCTCTGTGTTTGTGTACTCTCACTCTCGGCTACACGTGATGTTGTGCGAGTAAAGGTGTGTGAAGGTGCCATTATTTGGGTCAGTGATTAAGGTCACTCATATGTTGTCTTCTCAGCAGTGTGCTGGCATGTCTGTGGTCTGCAGAAGGTAATGAGGTGTGGCTGTGTTTCCTTTCACA[G/A]CCCGAGGAGCTGACCAACATCCTGGAGATCAGCAACATCGTCTTCACTAGCATGTTTGTCCTCGAAATGCTCTTCAAACTGCTGGCCTTTGGCATCTTCGGCTATATAAGGAACCCATATAACATCTTTGATGGGGTTATTGTTGTCATAAGGTAAGTTCTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTAAGTATGTATGTATGTATGTATGTATGTCCGTCTGTCTGTCTGTCTGTCATCTATCTATCTATCTATCTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCATCCATCCATCCATCCATCCATCCATCTATCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16182
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 |
---|---|---|---|---|---|
ENSDART00000085210 | Essential Splice Site | 690 | 2114 | 11 | 36 |
ENSDART00000085210 | Essential Splice Site | 690 | 2114 | 11 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 39902235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 39765595 |
GRCz11 | 3 | 39907453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCTGTGGTCTGCAGAAGGTAATGAGGTGTGGCTGTGTTTCCYTTCACA[G/A]CCCGAGGAGCTGACMAACATCCTGGAGATCAGCAACATCGTCTTCACTAG
Long Flanking Sequence:
GTAATTCTTCACTCTCAAGAGCTGAAGCGCTGTCTGCATCAGCAAATGCAAGAAGACCAATTCTCTGGCCCCGAAACTGCTTATGATGGACAGATTCTACAAGCTCTGTCCGTCTGATTGATCTGCGTTGCTCTGCTCTTAATAAAGGAGCTTATTATGCTTTAGGTTTGCTTTTGCTTATCCAAGCTCAGCAGCAGAGCCGTTTGTGTTGAAGCTGAACAATTGTAATTGCTTGGTAAGTGTGCTGACGGTTTGGCCCAGAGGTAATGCGTTACGTAAACTGTCCATTTATCATCTGAATGTGCTGAATGGTTTTGCGTATCTCTGTGTTTGTGTACTCTCACTCTCGGCTACACGTGATGTTGTGCGAGTAAAGGTGTGTGAAGGTGCCATTATTTGGGTCAGTGATTAAGGTCACTCATATGTTGTCTTCTCAGCAGTGTGCTGGCATGTCTGTGGTCTGCAGAAGGTAATGAGGTGTGGCTGTGTTTCCTTTCACA[G/A]CCCGAGGAGCTGACCAACATCCTGGAGATCAGCAACATCGTCTTCACTAGCATGTTTGTCCTCGAAATGCTCTTCAAACTGCTGGCCTTTGGCATCTTCGGCTATATAAGGAACCCATATAACATCTTTGATGGGGTTATTGTTGTCATAAGGTAAGTTCTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTATGTAAGTATGTATGTATGTATGTATGTATGTCCGTCTGTCTGTCTGTCTGTCATCTATCTATCTATCTATCTGTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCGTCCATCCATCCATCCATCCATCCATCCATCTATCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33266
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085210 | Nonsense | 810 | 2114 | 13 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 39904793)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 39768153 |
GRCz11 | 3 | 39910011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTTATTTTTTCTTTTGTCTGTAAAGCATACTCGGAATGCATCTGTTC[G/T]GATGCAAATTCAGCCTGAAGATGGAGAATGGAGACACTATTCCGGACAGG
Long Flanking Sequence:
CCATGTGTTTCTTTGTCAGTGTATGGGAGATCATCGGTCATGCGGATGGTGGTCTCTCAGTGCTGAGGACTTTTCGTCTCCTGAGGGTGCTCAAACTGGTGCGCTTCCTCCCTGCCCTGCGCAGACAGCTGCTTGTCCTGATGAAGACCATGGACAATGTGGCAACATTTTGCATGCTACTCATGCTCTTCATCTTCACTTTCAGGTGAAGAACACAACAATAACTCCTTCAATCATAACTGAGCTTGATTTGCAGCATCTCTAACTATAATGACTATAAAACTATACTAAGACAGTAGTAAAAACTATAAGACTATAATTTAGACAGACTATAAGACTATGAGATTATAGTCAAAATTAAAATAATTGCAGTTTGTATTAGATAACGCATGCTGCATTCATTCATTTTTGTTGCACATAATTGTGAGTTTTTTTCAGTTAAATTTAAATGCTTTTATTTTTTCTTTTGTCTGTAAAGCATACTCGGAATGCATCTGTTC[G/T]GATGCAAATTCAGCCTGAAGATGGAGAATGGAGACACTATTCCGGACAGGAAAAACTTTGATTCCCTGCTGTGGGCCATTGTCACTGTGTTTCAGGTCAGAATAGAAACAGTACTGGCTGTACCAGGGTTGTGCTATGTATAGAGCTGTTCTTAGTTGCAATGTATGAACACATGAAACATCAAAAGTAAAGTGTGTATAAATAATTGCTCATTTCAGTAAGGTAACCTTGTATTTTCAGATCTGTTTCAGCAATGATAAAGCCTTGTATTATCAAAATAATGAAACACTTTATTGCCAGAGTTGGTATTGTGGCTTTACAAATGGTCAGAGTATTGCATGTGTCTTTATATTTTAATAACATTTCCCCAAATGCAGTAAGTGCATTGCATTGTTTTCATTAGCGCACAGGCTATAAAGTTTATTGTGCAATGTAGGTGCTTGTCTTTAATGTTCGAATGCATAAAGCTCACATAAAGCTCATGTTTTAAATAATGAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17053
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 |
---|---|---|---|---|---|
ENSDART00000085210 | Nonsense | 1341 | 2114 | 23 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 39919369)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 39782729 |
GRCz11 | 3 | 39924587 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAACATCACCAATAAGTCTGACTGTCTTCRGGCAAACCTCAAATGGATC[A/T]GAAGAAAGTACAATTTTGACAACTTGGGACAGGYACTGTTTTCCTCAGAT
Long Flanking Sequence:
GAGGGTGAGTCATTCGATCGGTCATTCAGTCAACAGCAGCCTCTGGTGGGTTTACACAAGAATAGCAGATGCGAAAGGCACTCAGGAGAGAAATTTGAGATCTTAAAAAGCATACACAGTGGTCTCTGGTGGATTTAAAACAAAAACTGCAAAAAAATGTAGTTCCTGGGACATATTTGTCGCTTTCTAGAAATATATATTTAGAGGTACATTTTTAGAATGAATCTGAGTTAAAGAAATGCTCAGCTGTGAGCACTTCATGAACTGATGGAGCATTTAAAAAATGCAGAGCATGGTTTTCAGAGTGGTTTTTAAAGCAATTGCATCTGTCAGCACAGATATTGGGATATTAAATTAGATTTTTGCAATGAGCATGCTATGAACATGTTTGCTTTGATCAATTGCAGCTCTTCAAAGGAAAGTTTTTCCACTGTGAAGGCGGCGATACCAGAAACATCACCAATAAGTCTGACTGTCTTCAGGCAAACCTCAAATGGATC[A/T]GAAGAAAGTACAATTTTGACAACTTGGGACAGGTACTGTTTTCCTCAGATATCATTCATAGATTTTATATTTACATTTAGTCATATAGCAGACGGTTTAGTCCAAAATGATTTACTAATGAGGAAGGCATTAAGCAACTTATCCTTAAGAAGCAATACTCACAAGAAGGGCTACTACTACAAATTGTAGGTTTTGACTTTGTTATAAAATTAAAAGCTAAATGTGGGGGAATGAAAGTATAGAGAGGGGGTGTTTTGACACTGTGAAGAATAATAAAGTGACTGGCTGAATAAAAAAGTGAGGTCATGATGCTCGACCTTCAGAAAAAAAAAATTCTGCAGTAATATGGTCGAAATGATTCCCAGATTGCATATATGAGTCCTGTAATGGCACTGAATGAATGATGGTTCTCTCTTCCGCAGGCTCTCATGTCTCTTTTCGTGCTTTCCTGTAAGGATGGATGGGTCAATATAATGTATGATGGGTTGGATGCTGTTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17795
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 |
---|---|---|---|---|---|
ENSDART00000085210 | Essential Splice Site | 1601 | 2114 | 29 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 39937114)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 39800474 |
GRCz11 | 3 | 39942332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTACAGGCATGAGATCCCTACTCGACACCGTAATGCAAGCTTTACCACAG[G/A]TACCTGTTGTCTGTTTTATATTCAKTTATTMAAATGTGTAWATTKGGAAA
Long Flanking Sequence:
TTTTTGTAGAGATATTATATGAGAGGCTTGCTTTGTTTACTAAATAAAGTGGATCCTATTGGATTTGATTTGTGAACATTAAATAAAAGTTAAAAAGCTATTGTTAGTTGTGATACTCCTAAAACTATTCTGCATTAATCCACAGAGTTTTTACTAAATTCGTAGCAGAAATAACAAAAAATTTCCTCAGATTATGTCTGGCCCTACTTACTGTATAAGTCAAGAACATAGCGTTTGCATTAATTAATGTCATAGCATTAATGCTTGACAAATGATAAACTCTTTGCTAATGCTTATTAATTTATTTATAGTATGCAGATATTATAAAGTGTTTTTACTATTACAAATAGTCTGAGATGTGTTTTAATGCCAGAATTGTTGAGTTCAGTAATGACTATATGGACGTGGGATTGTGTGTTCTGACCACAGTGCTGAAGCTGTTAAAGATGGCTACAGGCATGAGATCCCTACTCGACACCGTAATGCAAGCTTTACCACAG[G/A]TACCTGTTGTCTGTTTTATATTCAGTTATTAAAATGTGTATATTTGGAAAAGTTTATATTTCGTCACCTTGGAATCGTAAGGTTCTATCTGCTTTCTAAATGATTTTGAGATGTTGAGCTTCAAAGTTTTTGCATTCCATATAGCAAACAAAATGTGTACCACAGTTCTCTTTCATACATTAACATGACATAGACCCTAAATGTGCTCTAAATCTAAAATTAGAGTAAATTGGAGTAAAAAAAAAACAGTAATGCACATAGAATCTTCTAATTAATCTAATTAATATGTTATCCTGATTTGTTCTCGTGCATACATTAAAAATGCTGATTGGCTCACAGAAAGAGCCTTGTAGAGACTTTGTAGATAAAATGTTTTTTGTTTTTTAAATAAAAAGTCTTAATGTAAACGACTTATAATAAAAAAACATCCCATAACATAAATAAGTTTTTGTCATTTAATATGAATATGTGAATAACTAAATTTTGACAAAAAAGTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10926
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 |
---|---|---|---|---|---|
ENSDART00000085210 | Essential Splice Site | 1668 | 2114 | 31 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 39940488)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 39803848 |
GRCz11 | 3 | 39945706 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YGACACTTTTCCGAGTATCAACTGGGGACAATTGGAATGGRATAATGAAG[G/A]TAAACTACAACACAGAAGTGCTAACTGTTTTCTATTGGTGCCATTTTAGT
Long Flanking Sequence:
TTGATGCTTGAAGTTTGCTCCTGCTTTGGCAGCGGTTTTGTGAGTTAGCCGCTAGGCTCGCACAGACATATCAATGCTACTTATATCCCTATGAGAGAGGCCTTTGGAATACGAATGACAGGATTATGCTTTCTCTTAAAGGGCAAGCACTGTAATTACTTTCATTAGCATTCAGCTTTAGAATCAATGCTAATTATTGTGTCAGACGTGTCTGGGGAAACGGCTCATTTGCTTCTTCAATGGTATTACAGGGGACTCTGTCAGGTTTTCTCCAATTTTAGAAACACATTCTGTGATGATCAAACTTTTTTGTGTGTTAAGGTGTTTAAAAGTATTTGAGTGTGTGTGTGTGTTTTTTTTACAAATATATTCATCTAGAATGCACAGAGAACAATCCGTGTGAAGGATTAAGTCCACATGCCACGTTTGAGAACTTTGGAATGGCATTTTTGACACTTTTCCGAGTATCAACTGGGGACAATTGGAATGGAATAATGAAG[G/A]TAAACTACAACACAGAAGTGCTAACTGTTTTCTATTGGTGCCATTTTAGTGATTGCTATGTTTCTTGCGTGCAGGACACTCTGCGAGAGTGCCTTCCTTCAGAGACGCAATGCCTCAGCTATCTACCCTGGGTCTCTCCAATCTATTTTGTAACCTTTGTTCTAATGGCTCAGTTTGTGCTGGTTAACGTGGTCGTAGCTGTGTTGATGAAACATCTGGAGGAGAGCAATAAAGAAGCTAAAGAGGATGCAGAAATGGATGCTGCGATCAAGTTGGCAATTTTGAAAGAAACTCGCCGTCTCAGCACCATCTCAGCCAGTGCCACTGCGGGACCAGAAGGCAGGGCAACTTATATCGAGCCACACCCAGATTCACCTGAGCAGGTAGTTTTGCCTGAATGGGGGGGGGGAAGTAATAGCATGTGTTTAAGAGGCATTTTAAAAGGATTGGTTCACCCAAAAATACAAATGATATTATTAATCTTTTTTTCATCAGAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13577
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085210 | Nonsense | 2107 | 2114 | 36 | 36 |
Genomic Location (Zv9):
Chromosome 3 (position 39945655)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 39809015 |
GRCz11 | 3 | 39950873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGAAAAAGTTGTCGGATAGCATGTTACTGCGGAGGAGGACACCATCCTA[T/G]GACCTGGCCCTGCAGCGGGACTCTYTGGACTTGCCGGAGAACCAGCTGTC
Long Flanking Sequence:
AGCCCCAGTGGCTCAATGTTTGACTCCGCTGACCCAACCGATGAGGAGGTGCGCCACATCAATAGCACAGCCCGCCTGTGGATCGGGGTTCATGCAGAAGCAAGGAGTCACTCCCTCTCTCCTTACAGCACCTCAGGGACGCTGCTTCCCATCCCCGTGAAAAACTGCAGCAGTGCTGCCAACTTAACCATCAAAGACCCCAAGAAGTGCTTCAGTGTGGACACTGAGGGTTTTCTGGAAAGACCCTACGCTTCTGATGACCATCGCAGGCACTCGATTGAGATTTGCTCCTCAGGAGACGATGGGCTGTTTGGTCAAGAACTCTGTGAAAAGAGGCACGTTCCCACGCGTGGAAAGTCTTTGCACATTCCCCGGAAGACAAAGATGAGCCCTCCCTGCATCTCCATCGAGCCCCCATTTGAAAAGGATGTTTCCCCCTCTCATGCGTCCATGAAAAAGTTGTCGGATAGCATGTTACTGCGGAGGAGGACACCATCCTA[T/G]GACCTGGCCCTGCAGCGGGACTCTCTGGACTTGCCGGAGAACCAGCTGTCAACCCAGCCACTCATCAAAGTAGAGCGACATCCCTCTCACTGTGCCGAGTATCTGTCCCTCCCACACCCCGCCCCAATGAGCGGTCTGGCAGGCGTTTTGTGTGAAAGCACGCAGCCGCCCCCCTTTGATAGCAGATATGAAGAATCCACGGACTTCGGCTCTGTAAACAGGACAGCTCAATGAGGGACGCTGGCTGACGCTAGCCAGATTTTACCGTCCGCACTCAAGGGTGCAGCAACTAGTTGAGCGGGGGATGACGACCTCTTTCTGTAGCCAAAGTTTTCTTTGTTTTTTCTTCAAATGTAATATCATCCTAAAAGCCAGCCAGAAATGGCAACCGATCCTAGTGCGGAACAGCATTTGATCTGACTGTGATTGGGCAAGGTGTTGAACACGGGATATGCAATTTCAGGTTTCCGAATGGAACTCTGGTTCTTATTTTAGTCCCA
Associated Phenotype:
Not determined