Busch Lab

ZMP

cacna1sb

Ensembl ID:
ENSDARG00000042552
ZFIN ID:
ZDB-GENE-051227-1
Description:
calcium channel, voltage-dependent, L type, alpha 1S subunit, b [Source:RefSeq peptide;Acc:NP_99989
Human Orthologue:
CACNA1S
Human Description:
calcium channel, voltage-dependent, L type, alpha 1S subunit [Source:HGNC Symbol;Acc:1397]
Mouse Orthologue:
Cacna1s
Mouse Description:
calcium channel, voltage-dependent, L type, alpha 1S subunit Gene [Source:MGI Symbol;Acc:MGI:88294]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa12580 Essential Splice Site Available for shipment Available now
sa27213 Nonsense Mutation detected in F1 DNA Not yet available
sa38692 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa34412 Nonsense Mutation detected in F1 DNA Not yet available
sa41219 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa1443 Essential Splice Site F2 line generated Not yet available
sa34413 Nonsense Mutation detected in F1 DNA Not yet available
sa34414 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12580
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062406 Essential Splice Site 74 1847 1 45
Genomic Location (Zv9):
Chromosome 8 (position 26620969)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 25748887
GRCz11 8 25768026
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTCAGAAACCCTTTCCGGAAGGCTTGCACCAACATTGTGGAATGGAAG[T/A]ATCCTTCGCAATTACGCTTGTTCTGGTTTTTCCAGCAGCTTCGGAGTGTG
Long Flanking Sequence:
ATTTAACCCTCAGTAGAGGCCAGCTGCGTCTAAATGCTCCCTGCCCCTCAGATGCCTCCTTGTCTGGTGTAGGTTTGCACAGGGGCCAAGAAGTTTGACTGTGCCTTCCACAGAGAGGGTGAGATAAGGGGTGGATGAAGCTTAGGACCAGACTGAAGATCTGACCTGGATTTAAGGAGGCCAAAGATTTGCTGAATACACTTTTTGGCCTAAAAAGAAAGCAATCATTCAGTTCTTTTTTTATTGGAATTTGGACAAATACATTTGGGAGATTGAGAATGGAGTCAGGCGGTGGTGGTGGTGGTGGAGGTCCTGGGGGTGGTGGAGTGGCAGGCTTGGCCTCGTTCATCATGAACGAAGAAGAACTGAAGAGAAAACAAAGGGAGAAGCTGAAGAAACTGCTGGCCACCGGAGGAAACCCTCGACCTCCACGTACATTGTTCTTCTTCAAGCTCAGAAACCCTTTCCGGAAGGCTTGCACCAACATTGTGGAATGGAAG[T/A]ATCCTTCGCAATTACGCTTGTTCTGGTTTTTCCAGCAGCTTCGGAGTGTGTTTTGGTGTTCATTGGTTAGGGTATTGAATGGTACAGTATGCTGAGATGGGCATGTTTTAGAAAGGCATCCGAGAGCTGTTTTCGCAAGCCAGAAAAAGCACACAAGCACGGCTCCCTAACCATGATTGATCTGTCAAGTGAGGACCATGAAATCGCCACGTTTCTTTTGTAATACCCAGGTTTAGTGTCTCTCAAGGTGCTGAAATTTGTGTCACAGTTGTGCACCTAAGGTGTTAAGCTTTTGTTATGAATCACACTTGCCATGGTCAATTGCAAGCTGTTAGATCAGGTCTTTAGGTGACTATTTACAGCTGGTCAGCAAATAAGACTGGTGTTAATTGTCACAATTTTCACTTTTTATTGTTATAACATGGCTTTATACGTTTTTTAGATTGATGGTTTTGTTTATGCACAAAAGGTATTTGTTTAAATGCTTCAAACAGCTAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27213
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
ENSDART00000062406 Nonsense 142 1847 3 45
Genomic Location (Zv9):
Chromosome 8 (position 26626742)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 25754660
GRCz11 8 25773799
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTAAAGATAATAGCATACGGCCTCTTGTTCCATGAAGGAGCCTATTTA[C/T]GAAATTGTTGGAATATATTGGACTTTGTCATTGTGTTCATGGGGTAAGAT
Long Flanking Sequence:
GATTACAGCTGAACCACTGAAGTCCCTTGGATGTTTTGACATCTTTTTGGACTCTGAATGTCTTGAAACTATCTATAGAGGATGAGGGAGCTCTTGGATTTCATCTTAAAGTAACTCAATTTGTGTTCAATCAATGGGCTCATGGGATTGGAATGAAGAAAGGCAAGTAATAAATTTTTGGTTGAACTAACACTTTATAATGAGTAATATGCTATTTTATTTGATCTTCTGAAAGTGCATTGACTTTAGTCTTAGACCTTTGAAAGCAGATATTTCATTGTCCAAACTCAAGGGGTCACATCTCAAATACCCCTTGGAATGTAATGATTGTGAACAAAATTTCAAAACGCCTGTTTATCATCGTGTTTTACCTAATACCCTCCAACACTGTGTTTTCTTTGCAGGAGAGTCTGGAGTACATCTTTCTGGTCATTTTCACTCTGGAGTGCTTCTTAAAGATAATAGCATACGGCCTCTTGTTCCATGAAGGAGCCTATTTA[C/T]GAAATTGTTGGAATATATTGGACTTTGTCATTGTGTTCATGGGGTAAGATGAAATTTGATGCTTCCAAAAACACAAAACATGCACTGCTGTCCACTGAAATAACTGCTTAATCAGTCTTGAAATCAGTTTGATAGTAGAATTGTTGTGGTAAGAATGGAATAGCTTACACTAAAAAAATATTAAACTCACTTTGTCTTATTTTGTATATCTTTTTTTGTATTAGATCGTGTTTATATCATCATTGGGATGGAAGAATGTAGTATATTTGCTCTCAGCAGTGTATACAGTGTCTCAATGGTCATTATTAGTTTATTGCCACATTTTTTACTTCATGAGTGTTCATGAGTTCTCTATTATAAGATGGCTCTACTTCATTGAACTGTATAAATCTTAGCATTTTTATTAACTGTATTTGATATTTTTTCCAATAATCCTCTTTTTAAACGATTTCCAGGCTCTTCACACTTGTTGTAGACACCATCGACACAATAACAGGAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38692
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
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062406 Essential Splice Site 628 1847 12 45
Genomic Location (Zv9):
Chromosome 8 (position 26633483)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 25761401
GRCz11 8 25780540
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGCAGCAACTTCGACAACTTCCCACAGGCCCTCATCAGTGTCTTCCAGG[T/C]ACATCAACCGCTATTTCAAACTACAATCTCATTTATCACTGAGTAGTCAG
Long Flanking Sequence:
GTGTGTGTTCTAATTTCAGTTGCTCAACTTTGATGTTCAATAAATATTCATTGATAGTAGATAGTGTGTGTTTACTTGAATTATTTTAAAACTAATTAATGCACCCTTCATTCAGAAATCTCTCACTTGTAATATGTGAGCACATGTACTGTACAAAACCTGTCAGTGAACGATGAGGGCAAAAAACTATAATAAAATAAATAAATAAATAAATAAATAATGGGGATAATATCTCCCATACATAAAGCACCAGCTTCCTTCTTTAAGCTATTTCATCTCATTGTTTTCCAGGTACTGGACATCTCTTAATAACTTAGTAGTATCTCTACTAAACTCAGTGAAATCCATTGCCTCCCTGCTCCTGCTCCTTTTTCTCTTCATCGTCATCTTCGCTCTGCTGGGGATGCAGGTGTTTGGTGGCAAATTCAACTTTCCTGACAGACCGATCCAGCGCAGCAACTTCGACAACTTCCCACAGGCCCTCATCAGTGTCTTCCAGG[T/C]ACATCAACCGCTATTTCAAACTACAATCTCATTTATCACTGAGTAGTCAGATAATGTGAAGCTTCACCTTTGTTTTCAGGTCCTGACCGGAGAGGAATGGGACACAATCATGTATAATGGCATAATGGCTCATGGTGGACCCAAATCTCCAGGAATCCTCGTCAGCATTTACTTTATAATACTATATGTCTGTGGAAACTGTATCCTTTTGAATGACATGCTTTTGTGTATTTGTTAAGCATTCGGCAGAACTCTAAAAGCAAAACATTGAATATAATATGATAGTGGTGAATATGTGTGTGAATGAGAGTGTGTATGGGTGTTTCCCAGTACTGGATTGCAGCTGGAAGGGCATCTGCTGCATAAAACATATTGCTGGTTCATTCCGCTGATAAATCAGGGACTAAGCTGAAGGAAAATGAATGAAAGAATTGAAGTTTGTTGTTGTGAGAACATTTTGGGGCTTCTTCCTTAGCAATTTATTGGTCAGTTGTTCTCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34412
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
ENSDART00000062406 Nonsense 693 1847 14 45
Genomic Location (Zv9):
Chromosome 8 (position 26634045)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 25761963
GRCz11 8 25781102
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCCATCGCTGTGGACAATCTTGCCGAAGCTGAGAGTCTGGCAGCCGCA[C/T]AGAAAGAGAGAGCGGAGGAAAGAGCCAGAAAAAAGCTCATGAAGTAAGGC
Long Flanking Sequence:
CTTCACCTTTGTTTTCAGGTCCTGACCGGAGAGGAATGGGACACAATCATGTATAATGGCATAATGGCTCATGGTGGACCCAAATCTCCAGGAATCCTCGTCAGCATTTACTTTATAATACTATATGTCTGTGGAAACTGTATCCTTTTGAATGACATGCTTTTGTGTATTTGTTAAGCATTCGGCAGAACTCTAAAAGCAAAACATTGAATATAATATGATAGTGGTGAATATGTGTGTGAATGAGAGTGTGTATGGGTGTTTCCCAGTACTGGATTGCAGCTGGAAGGGCATCTGCTGCATAAAACATATTGCTGGTTCATTCCGCTGATAAATCAGGGACTAAGCTGAAGGAAAATGAATGAAAGAATTGAAGTTTGTTGTTGTGAGAACATTTTGGGGCTTCTTCCTTAGCAATTTATTGGTCAGTTGTTCTCTTGAACGTGTTTTTGGCCATCGCTGTGGACAATCTTGCCGAAGCTGAGAGTCTGGCAGCCGCA[C/T]AGAAAGAGAGAGCGGAGGAAAGAGCCAGAAAAAAGCTCATGAAGTAAGGCTTTTGTCACACCAAACATGTCACAAAACCTTGGACACTGAGATTGATTAATATGAATTAACAGTTAATTAATATAACAAAATCATTCAGTAGATTACAGCAGGGGTGTCCAAACTCGGTCCTGGAGGGCAGGTGTCCTGCATGGTTTAGCTCCAACTTCCTCCAACACACCTGCCTAGAAGTCCAGTATACCTAGAAAGAGCTTGATTAGTTGGTTCAGGTGTGTTTAATTGGGGTTGGAACTAAAATAGGCAGGAGATAGGCCCTCTAGGACCGAGTTTGGACACCACTGGATTACAGCAATCATTTGTTTTTATATTCCACTTTGTATTCAGCACTCAAATTCAAACACAGGCTCATTGGAAATATGTGCTTACATTATTTTGAAACCGCAAAAAAAGCATATACATTTATTGCAGTTTCTAGGTAAAATTAATGCATGTTGCCAACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41219
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
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062406 Essential Splice Site 763 1847 16 45
Genomic Location (Zv9):
Chromosome 8 (position 26636806)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 25764724
GRCz11 8 25783863
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAATGTGAATGAAGTGAAGGACCCCTTTCCTCCTGCTGACTTTCCAGG[T/C]AAGGCTGAAAGCCTCCGACACAAGGGCTTAAATATCATCAGAGGGCTCTA
Long Flanking Sequence:
ATTTGATCGAAAATAATTATAATAAACTAAATATTAAAATAACAATTATTTAATTGAATCAGAAAATGTTGTTAAAATTATTTATGGTTATTGCATTTTATCAAGTCAATAGTCACCGGCAAGTTGTCAATATGTTAATTTCAGACCTTGTATTTATTATTGAACAACATTTTCGTTTTCATAAGACCATTGCCAGAGAAAACTGAGGAGGAGAAAGCCCTGATGGCCAAGAGACTAATGGAGTCCAGGCAAAAAACTGAAGGAATGCCCACCACAGCGAAGGTATGACTAATATCTCTCTTTTTAGATCCGCTGGTCACCCTTTTAGCAAGCACTATAACGATTATCCAAGATATTGTGTCCTCAAATTCAAGACACTGATGCTAGCTTAGTGTCTGCTTAATGAACAGTGTATACTTTGGTCTCCAGCTCAAGATTGACGAGTTTGAATCAAATGTGAATGAAGTGAAGGACCCCTTTCCTCCTGCTGACTTTCCAGG[T/C]AAGGCTGAAAGCCTCCGACACAAGGGCTTAAATATCATCAGAGGGCTCTACACTTCACAAAAATGCTGGCTCAGACCTCATGGTACAGCACTAAACATGTAAAGGATGAAGTTCAAAGATAGCTGAACTATTATAAGTCCATTTTATTATTAGCTCCAGCCTCCAAGCTCATTTATGGGGCACATTTTAAACCACACTGCTGGCAATTTCCACGTGGTTATAAAAGAGACAAGCTTTACAGTGTAAACTCTTCATGATCAATGCTAATACAAAAAAAAAAAAACTAATACTTTAATACATTATGGCTTTAATTGTTTATTAATTAGAGTAAAATTAGAATAAAACAACTTTCCATTTAAAAGATGTATTAACACCATGATGTATCAGTACCACTGACTATGATTAATAAATGCTGTAGAAGTCTTGTTAGCTCAAGTTAAATAATGTACTATTAAAATGCTGACAAATGAAAGCTTGTCAGAAAGGGTTAGCATTAAACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1443
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000062406 Essential Splice Site 870 1847 19 45
Genomic Location (Zv9):
Chromosome 8 (position 26640031)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 25767949
GRCz11 8 25787088
KASP Assay ID:
554-1369.1 (used for ordering genotyping assays)
KASP Sequence:
ACGCAGACATCGTCTTCACAACGGTCTTCACCATTGAGATTGTGCTGAAG[G/A]TAATGCACTTGTCAGCTTTATTTAACCTTCAGATTTGTGATTTGGCTGAC
Long Flanking Sequence:
ATGTGACCCTGAGGCACAATTTTAAGAAGAGACACTAATAATATTTCCATTGATTTATGGCTTGGATTGGACAATATTCAGCTCTGATACAACTTTTTAAATATCTGGAGTCTGAGGGTGCAAAAAAAAAAACTGAATATTGAAAAAACTCACCTTTAAAGTTGTTCAAGTTTTTAGCAAAGCACATTGCTAATCAAAAAAATAAGTTTTAATAAATTTACACAATACATTTACAAAAAAAATCTTCATAAAAGACGATCTTCCTTTTATATTCTAATGACTTTATGCATAAAAGAAATCCATAATTTTGACGCGTACAGTGTATTTTATAACATAACATCAGGTTTGTGGTCCAGAGTCACATATACAGTATTGCCTTGACTAAACTTTTGACTAAATCTACACATTCATAAATATATGCTTTGATTCATTGATTTCAGGTCTTGGCTTACGCAGACATCGTCTTCACAACGGTCTTCACCATTGAGATTGTGCTGAAG[G/A]TAATGCACTTGTCAGCTTTATTTAACCTTCAGATTTGTGATTTGGCTGACATTTACTTGAGCGCTGACTCGTGTATTTTTAGATGACGGTGTATGGAGCGTTCCTGCATCCCGGCTCCTTCTGCCGAAACTCCTTCAACATTCTAGATCTCATTGTTGTGGCCGTTTCTCTCCTGTCTATGGGAATGGAGTAAGTTTTGTCATATTATATGTTTTTTTCAGTGTTTCCCTCCCACTCATTCTGGTATTGCTTTGACAAATACATTTCTATAATAACTTTTAACAGCTGCTGTTTTGAGATGGTGTCCTATTAGCAAACATTAATTTATTCATATATTCAATTTCCATCGGCTTAGTCTCTGATTTATCAGAGTTTGCCACAGCAGAATGAACCGCTGATTATTTTGGCATATGTTTTACGCAACGGATGCCCTTCCAGCAGCAACCTAGTACTGGAAAACACCCATACACTTATTCACACACACACTACGGCCAATTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34413
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
ENSDART00000062406 Nonsense 919 1847 21 45
Genomic Location (Zv9):
Chromosome 8 (position 26641792)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 25769710
GRCz11 8 25788849
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTATTTCAGGTCTAGTACCATCTCAGTAGTGAAGATTCTCAGGGTGT[T/A]GAGGGTACTCAGACCTCTAAGAGCCATCAACAGAGCCAAAGGATTGAAGG
Long Flanking Sequence:
AGATTTTATTGGGAGTCCATTGCAATATTCTGTGCTTCTGAATAGCTGTCATATCATGTCTTTTGCGAACAACCAAATTGCTTGTTGCCAAATTCTTGTCTAAAATTCTTGTATAGTGTTCCCTCCTCTGTAAAGGGTTAAATTGTTGGGTAAGGGGTTGTTCTGGAAAAAATAAATTAAAAATCATAAAGTAAACAAAAAAAATCTTGTATAATAAGTGCAACTAGTTTACTTTGGTGATTCTTAAATGATCAAACCTTATGAGGTAGTTTCTTTCAAGTTAAACAAAAAAAACAATGTGCAGCCTATATTGTCTAAGCAATCCTCAAATATTTTTCTAAACTCATTTATGCATATAAATCTTTTTTTGTGAAATATATATTTGTGAAATATTTGAATGCTTAAGTCGGTTGAAGAAGGTTGGATGTTGGCAAGTGACCGGATTGTATTATTGTATTTCAGGTCTAGTACCATCTCAGTAGTGAAGATTCTCAGGGTGT[T/A]GAGGGTACTCAGACCTCTAAGAGCCATCAACAGAGCCAAAGGATTGAAGGTGTGTATATATTCAGCATCCCAACTTAAGCTGCACTGATGGTTTGTGCAGTGGCATTAATGTCTGTTTATATTCGAAATACCGCCACTAAAATTGTGCTTGGCCTTGTGTTCTACCAAAGCATTTTTTTTCCTAACGTTAGCATTGTTTTTAAAAGGAGTGCTGAAATTTTTAAATGTTGCATATAGGATGAGGTGCTGAGCATCTATTTACACTTGAAGCTGAAGTGTGTTTAACATTGATTAAAATGCTTTGCTCAAGACTGTCAATGTTTAATTATTCTCCCAATTGACATGCCACTTAAGACCTCGTATCCTTCCAGTAAATCATGTCATATCCATGACATTGGCGTGACTCAATGACTGCATTTCGACTTTGTGATTTGTGGGGGAAAAAGTATTTGTAGAATCATATAAAATGCTGCCTCCACCTTAAAAACAGACCACCAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34414
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
ENSDART00000062406 Nonsense 1821 1847 45 45
Genomic Location (Zv9):
Chromosome 8 (position 26660905)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 25788823
GRCz11 8 25807962
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATTGGCTTGCAGGATATAGAGAGCGTGGCTCAGGGTATTGTCAATGGG[C/T]AGAGCGGCAAGGTAACCAAACGCAAGCGACGTCCTATCCCTGTTCCTCCC
Long Flanking Sequence:
TTATTTTCTTGTGCAACCAATAGGAGACTCCAGCTTGTATGTGGGCGGAGCCTCAAATGTTAATGACAGGCGGCTGTCAGATTTCAACGTGAAGACTAATTCTACACAGGTTTGAACACAAAACACATCATTATAATAAGCTTAGCAACTGATTTTCTTTTCTGACTCATTTGTTTGCATGTGACTCTCACAGTTCCCTTATAATCCCTCATGTGAAGAATCAAAGAACCAGAGATCAGCAGCAGAAGCCTCACCAGCCACCGACAAACTCATTCAGCAGGTAAACAATATGCATGTCCTCTTCATATTCATTCCAGACTTTCCTCTGAACTTTGATTAATCTGTATTTTGCCATGAATTCTCAGGCACTGAGAGATGGTGGTCTGGAGTCGTTGGCTGAAGACCCACAGTTTGTATCTGTGACCAGAAAGGAGCTGGCAGAAGCCGTTAATATTGGCTTGCAGGATATAGAGAGCGTGGCTCAGGGTATTGTCAATGGG[C/T]AGAGCGGCAAGGTAACCAAACGCAAGCGACGTCCTATCCCTGTTCCTCCCAGCAAAACCAAGGAAGCCACAAGTGCAGTGTAAACACATACTGAGAGACTTTTAACAAAACCATGAGACACCATCGCCCTGAGGCTTCAGCCATTGTTTAAAATCACAGACGTAACAGTTTACGAGCAGGTAGTGATTAAGCTGTGCTGTTTTTAAAGATGGTATTTTGGTTTAGAGAAATAATGTTTCCAAAGGACACGTACCATAATGCTGTTTCAATGAGGTCTTGTGATTTTGATTTCTGATGGCTACTCTGATTCAGGTTTGTTTTTTGGTAAGCGATTATACCAAACGTCCTCAATAAAGTGTTCACACTTCTGTTCTGTGAACATCTATAATTGACTGTGTGACAATACAGACAATCATCTGAAGCGTTGTAATCTGTGGACATGTCTAAAAGGCAAGTCTTTTTATTTCTTTACTTTGTTTAAACTGCGCAGAATGGTTTAC
Associated Phenotype:
Not determined