ZMP
CADPS (1 of 2)
Ensembl ID:
Description:
Ca++-dependent secretion activator [Source:HGNC Symbol;Acc:1426]
Human Orthologue:
CADPS
Human Description:
Ca++-dependent secretion activator [Source:HGNC Symbol;Acc:1426]
Mouse Orthologue:
Cadps
Mouse Description:
Ca2+-dependent secretion activator Gene [Source:MGI Symbol;Acc:MGI:1350922]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27764 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31824 | Nonsense | Available for shipment | Available now |
sa35069 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa27765 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21886 | Nonsense | Available for shipment | Available now |
sa15647 | Essential Splice Site | Available for shipment | Available now |
sa41815 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14101 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa27764
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 |
---|---|---|---|---|---|
ENSDART00000029680 | Nonsense | 96 | 1316 | 1 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 20201706)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 19619020 |
GRCz11 | 11 | 19781362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAGAAGAGGCTCCAGCTGTACGTCTTTGTGATGCGGTGTATTGCCTA[T/A]CCTTTTAATGCAAAACAGCCGACCGACATGGCGAGGCGACAGCAAAAGGT
Long Flanking Sequence:
GTTAAACACGTAAGCAGCAACAATTTAATTCGGTGGAAGACTACTGGCTGTTGGAGCAGCTTTTTTCACTCGCAGTGAGGGTAAGTGACACTTTTGATGTCGCGTTTGGATGGAAATAAGCGCCTTCGGTACTTTTCCGAGTTACCGAGGGGCTTTTGATAGTAAACAACATTTCTCTCGTTTGATTTCAGGGAAGCGAGAACTTGCGTTGAAATGTTGGACCCGTCATCCAGCGAGGAGGAGGCGGATGAGGTTGTGGAAGAAGAGCGAAAAGTGGTGGCGGCGCCCAAGGCTGGTGGTCCTCGGGTGTCTTCAAGCCGGACCAGCGAAAGCTCTGGTGGGCTGCAGCCGAGCCGAAGCACCAATGCCCGGCCGACGAGCCCCAGTCCCTCAGTGGCGGTCGAGAAGGAAAAGGATGATTTAGAAAAGATGCAGAGGGAGGAAGAGGAGAGGAAGAAGAGGCTCCAGCTGTACGTCTTTGTGATGCGGTGTATTGCCTA[T/A]CCTTTTAATGCAAAACAGCCGACCGACATGGCGAGGCGACAGCAAAAGGTAAGAGGGCAAAGTCGCATGCAACAGATTGCTGTGCAAATGAATTGAAGAATGGGTGAGCAGCAACTGCAGGCTGTGGAAAAACACAGTTTTAGCGTATTGGGGATGATTGTTTCAGCCCTAAACTAATGCAACATGAAGATGCATCAGGAAATTTATTTATTCATATTTTCCAGTGCATAAGAAATCAACATTATGCTTGATTTGTTTTTTCATAATCAAGAAGAAATTAATGTTTACCTTGCATTAGTAGCTTTCATTTGTACTTTTAGATTGTGTTAAAGATGAAAGTGGGTTTTTAGTATAGTATCAGAACAATAAAAGTGTAATATACATTTAATTTCCCCCATACTTTAGAATGTGTCCAGTTTAATTAAAAGGAAATATCAGAATCACTATCATACATTTTTACAGTGATTTATGGAAGAGAACCACTAAAATTTGCACCGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31824
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 |
---|---|---|---|---|---|
ENSDART00000029680 | Nonsense | 149 | 1316 | 2 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 20251084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 19668398 |
GRCz11 | 11 | 19830740 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCAGATTGTAGCCGATGAGGCCTTCATCAATGCAGTCCAAAGCTACTA[T/A]GAGGTTTGGCTTCAATTTTATTCATCAACGCAACAAGTCTGGACTTGCAC
Long Flanking Sequence:
AGCCACACAATATTTGCAATTCTGTTTGCGAATGTTTAGTTCACTCAAAAATTCTCCATGTTTCAAACTTTTATGAGTTACTTTATTCTCTTTAACACAAAATATTTATTTAAGAATGTTGGAAAGCAGCAGCCATTTACTTGCAAAATAGTTTCTGTTCTTATACTGTCGATGTCAGTGATTACCGGTTTTCCAGCATTCTTCATAATATCAGATAACAATAATAACAGAAGAAATAAATGTATAACTTGAAAACTTGAGAGTGAGTAAATGATGAGAAACATCTGGATTCTTAAAAGTTTTTTAATAGTTTTTTCTTTTTTTTTGGTGTCACATTGTATACATAATAAATGAAAATCTGTCTCTCTCTCCGATGATTTCTCTTCTCAGATCAGCAAGCAGCATCTTCAAACAGTGAAAGAGCGTTTCCAGGCCTTTCTCAATGGAGACACTCAGATTGTAGCCGATGAGGCCTTCATCAATGCAGTCCAAAGCTACTA[T/A]GAGGTTTGGCTTCAATTTTATTCATCAACGCAACAAGTCTGGACTTGCACTGGATCTCAAACCAATTCTTCTTTCGATAAAATCCTTTGCACGCAAACCTTGTATAATGTCATCAAAAAAGATGTTTACTAAATTGAAAGAGCGTTTCTGTGTGTTTTTAATAGAAGATTCCTAAACTCAAGAAAGACTGTATTTATTATATAGCTGTGGTAAAAAATAAATAGAAAGAACTAAAAAAAAGTTTTTTCGAAAAAGGCTAGATCATTTATTTTCTCATATTTAAAATAAAATTGTCATTTATGTCAAAAATGTCAATTTTATGTAATGTTTTTGCAAACAGTCTGACTAATTTCTATTTTCTGAATACCAAAAATGCCCTAAATGACAATATTTTTAATTTAAATTAGGAAGAAATGTTATCAGATCTTAATCTAAAACTAATTTAAACGTTTTAAACATGTAGTTAAAACAATTCTTGTCAGTTTTGATCAGTTTAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35069
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 |
---|---|---|---|---|---|
ENSDART00000029680 | Essential Splice Site | 366 | 1316 | 5 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 20297384)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 19714698 |
GRCz11 | 11 | 19877040 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAGAACCAGCTCTCCAAGTCTGACGTTGTTTTGTCTTTCACACTGGAGG[T/A]AAGTGTTCCTGTTTAACTGCATGGATTAGAGTGTCACTTTTTCCGGGAAT
Long Flanking Sequence:
AGAATTTTTAGATATTTGGACTAGAAACAAGACAAAACATCCAAGTAAAAAAACATTTATTGCAATGTTGTCATTGCTTGCTGTACTTGCCTTGCACTATTTGCTCTATATTTCTTTACATGTTTCACTTGCCATTGTATGTGTGTGCTTGTTGATTTTTTGTACTGGAAGTCAAAAAAAAAAATGTAGATGCACATTGTACAATGCCAATTAAGACATTCTAATTCTAAAGAATTGTTTTTTCTCTCTTTACCTGCTTGAACAGGCTGGCCGCTTCCCTAAGTTTGTGTCCAGGGACATGGAGGCCATGTACATTGAGGAGCTGAAGTCATCGGTGAACCTGCTGATGGCCAATCTGGAAAGCATGCCAGTGTCCAAAGGAGGAGAGTTTAAACTGCAGAAGCTCAAAAGAGGCCACAACACATCCATCATTGACATGGGCCAGGAGGACGAGAACCAGCTCTCCAAGTCTGACGTTGTTTTGTCTTTCACACTGGAGG[T/A]AAGTGTTCCTGTTTAACTGCATGGATTAGAGTGTCACTTTTTCCGGGAATGTTGTTCAAAACATGACCTCGTGACACTCTAAACAAGGAGATCTCATAGGTATCGATGTCAAGACTGCAGTTTATAACGGATTGGCTGATCACCAAGCATGTAGAAGTTCATTTCTACAATGAACAAAATGCTGTTTAAAGTTTATATTATAGAAAGTGTGGTGTATATTTCTGGATTAGTGTAATATCCCTGTCTAAAAAAGCACTGACTGTATTCAAACCACAAGAGACAAACACTTTGATATACATCATTTATCTTTCAGCTTAGGGTGAAATTATTTTGTGGGTTGACAACAATTTAGGACAAATATGGCGGCATATGAAGGAAAAGCAGGATGTTATGGATAGTTTGTAACTTATTAGCATGATGTTAGTTTTATAAAACGTCTTTGAGTTTTTTTAGATCCTTTTTGTCAAAATTTAGCTATAGCTGAGGTAAGTGACAAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27765
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 |
---|---|---|---|---|---|
ENSDART00000029680 | Nonsense | 386 | 1316 | 6 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 20304069)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 19721383 |
GRCz11 | 11 | 19883725 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGGTACAGGGTCTGAAGTCTTTAGCACCAAACCGAATTGTTTACTG[C/A]ACCATGGAGGTGGAAGGAGGACAGAAACTTCAGACAGATCAAGCAGAGGC
Long Flanking Sequence:
TGTATGTATCCTTGTTATTGTATGCTTTATCACAAACATCTAACAATAATTACAATTTAGTTCAGTAGCAGATTGTAGACAGTCTTTTGTGGCTGTTTGTGGCATTATATTTCACCAAATTAGTTTTTAAAAGCAATTGAAAATGAAAACAATTCAATACAGTGCATTTTGACTACCTCTAAAAGTGTTTAAATCATATTAGATCCTGTGTACTGCTACAGCATGTACAGCATTATCCGTTTGTGATTGGATTGACAAAAACACATATTACTACTAGGTGTAAAGAGAGCCTTGAATGACAGAAATAACTACTGTACGGCTGCCAACGCAACACATTTTCCTTGACTTTGATAACATCAGCTATTTTTGATTGTATTTTCTACTAGGCAGTCATTTTTTAAGAGTCTTTTTTTCATTGCTCTTTTCATGTTTACTTCACAGGTGGTGATCATGGAGGTACAGGGTCTGAAGTCTTTAGCACCAAACCGAATTGTTTACTG[C/A]ACCATGGAGGTGGAAGGAGGACAGAAACTTCAGACAGATCAAGCAGAGGCCTCTAAACCAACGTAAGTCTCTTGCCAAGCATAATTTTTTTGTTTCTACCTCAACGTTATATGATGTGCATTGTTGCATGCTCCCATTTTCAGAAGCGCTGATTCTGGAAGAATTTTCCATTAATTTTTCTCATAGGGATTTTTATAAAAGTCTTTAAGCATTACAATCAACGAACCAAACCAACCAGTCCTAAGAAACATCACAACATTAACAATTATTGATTTAAAGGGCTATGAAACCCCCCACTACATGTGCACTACATCTGATTTTCACACCGGCAACACAAACACAGATGCAGGGGAGATAGACAGAGAGCAGCATTTACAGTGGATCTGAGAGCTGTGTGGAAGTGGAGGATTTTTAGTCCATAATATTGTAGAGATATTACTGTAAACTTAGTAACGAAATCATTTTGACTAAATTATGTCTTTAAAAACTAAGAGTAATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21886
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 |
---|---|---|---|---|---|
ENSDART00000029680 | Nonsense | 397 | 1316 | 6 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 20304100)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 19721414 |
GRCz11 | 11 | 19883756 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAACCGAATTGTTTACTGCACCATGGAGGTGGAAGGAGGACAGAAACTT[C/T]AGACAGATCAAGCAGAGGCCTCTAAACCAACGTAAGTCTCTTGCCAAGCA
Long Flanking Sequence:
ACAAACATCTAACAATAATTACAATTTAGTTCAGTAGCAGATTGTAGACAGTCTTTTGTGGCTGTTTGTGGCATTATATTTCACCAAATTAGTTTTTAAAAGCAATTGAAAATGAAAACAATTCAATACAGTGCATTTTGACTACCTCTAAAAGTGTTTAAATCATATTAGATCCTGTGTACTGCTACAGCATGTACAGCATTATCCGTTTGTGATTGGATTGACAAAAACACATATTACTACTAGGTGTAAAGAGAGCCTTGAATGACAGAAATAACTACTGTACGGCTGCCAACGCAACACATTTTCCTTGACTTTGATAACATCAGCTATTTTTGATTGTATTTTCTACTAGGCAGTCATTTTTTAAGAGTCTTTTTTTCATTGCTCTTTTCATGTTTACTTCACAGGTGGTGATCATGGAGGTACAGGGTCTGAAGTCTTTAGCACCAAACCGAATTGTTTACTGCACCATGGAGGTGGAAGGAGGACAGAAACTT[C/T]AGACAGATCAAGCAGAGGCCTCTAAACCAACGTAAGTCTCTTGCCAAGCATAATTTTTTTGTTTCTACCTCAACGTTATATGATGTGCATTGTTGCATGCTCCCATTTTCAGAAGCGCTGATTCTGGAAGAATTTTCCATTAATTTTTCTCATAGGGATTTTTATAAAAGTCTTTAAGCATTACAATCAACGAACCAAACCAACCAGTCCTAAGAAACATCACAACATTAACAATTATTGATTTAAAGGGCTATGAAACCCCCCACTACATGTGCACTACATCTGATTTTCACACCGGCAACACAAACACAGATGCAGGGGAGATAGACAGAGAGCAGCATTTACAGTGGATCTGAGAGCTGTGTGGAAGTGGAGGATTTTTAGTCCATAATATTGTAGAGATATTACTGTAAACTTAGTAACGAAATCATTTTGACTAAATTATGTCTTTAAAAACTAAGAGTAATGCTGACTTCACTTACTAACTTTGCCATCAAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15647
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029680 | Essential Splice Site | 784 | 1316 | 16 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 20385170)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 19802484 |
GRCz11 | 11 | 19964826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCCAGCTACTCTCAAAAGTGAGCATGCAGTTGATTTGTGRTGTTTTTC[A/T]GGTCCTGATGAARGACATTGTGACCCCGGTTCCTCAGGATGAGGTAAAGG
Long Flanking Sequence:
TAAACACATTTTAAATCTAATATTTTATAACTAATTTATTTTTTTCTTTGTCATGATGAAGGTACAAAATGTTTTCCTAGTTATTTTGCAAGATACTAGTATTCCGCTTAAAGCGCACTTTAGAGACTTAACTAGGCAATTTAGGTCACTCAAGTTAGTTTAAGCAAGTCCTGGGATAACTGTGGTTTATTTTATAGCCAATTGTAAAAAATAAAACAATTTAGGGGCCTAACAATATTGACATTTTCTTTTATAAACTGTTTTTATTCCAGCCAAACTAAATGAAACAAGGCTCTTTTTTACAGAAGAAAATAGTTATTAAATAATATAGGAAATTTTGTGAAAATGTCCTTGTTCAGAACTTGGTAATTGAAAATAATTGTAACTAAAAATACAGGAGGGCTATTATGTTAATTATATTGAATAAGTAAATATTTGATAAGTTTAAATAACCCAGCTACTCTCAAAAGTGAGCATGCAGTTGATTTGTGATGTTTTTC[A/T]GGTCCTGATGAAGGACATTGTGACCCCGGTTCCTCAGGATGAGGTAAAGGCTGTGATCCGCAAGTGTCTGGAGCAGGCAGCTTTAGTCAATTATCAGCGCCTCTCAGAATATGCCAAGGTGGAAGGTAGGAAGCTTGTGTTTCTACTCCTCTTCAGCAACACAGTGCATATTCCTGTCTCTGAAACTGTGCTTAACAACAGTGATGATTAACTAACCCCCATTATACAGAAGTCGTGCTGAAATGCAACTGATATTGTTTATTTCAAAACAGGAAAGTTCAGGAGAACTCATTAAAAGTCAATATGTTATTTTGGGATTTTTCAAATAAGTTTATAAGTTAAATAAATAAATATAATATTATGAATCAATTTTTTTTATTTGTAATGTTTATATGATTTCATGTTGTTATTATTATTATTATTATTATTATTATTGTTATTATTATTATTATAGAAGCTATAAGCTGCAGATTTATAAAACTGTGTGGTAATAAATATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41815
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029680 | Splice Site, Nonsense | 927 | 1316 | 21 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 20412030)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 19829344 |
GRCz11 | 11 | 19991686 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTTGCTGTATGTCAGCACACATTTAGTCTGTTCTTCCCTCTTTCAGA[T/A]AATCTGTGTAATGGGAAGTTTCACAAGCACCTGCAGGATCTGTTTGCTCC
Long Flanking Sequence:
ATCAGCAGCACCGCTCAAATGGCTAATAGAAGAAGAGCAATCAGAAAGACAAACAAACAAACAAACACACACACACACTGCATACAAACCAGTTAACTTCACTATAGTTTCACTATAATAAGTTATAGTTATACTCTATAGTTTCACTAAAGTTAGACCTTTATTTACTGAAGCACAAGACAATGTTTATGACAATTCTGTATAAAAATATAGGGTTTTTTTTTGCATTTTTGAGGTTATTTTTATGAGCAATTGTGCATTGTATGTTTGGTAAAGCGTTCTGTTGTATATAGTTTTTGTTTATTTTGTTTCATTTGAATTGTTTGCTCAAAGTTTTGTAACAATTTAGCACTTTACTATTTGCTATAAAACACATTTCAGAGCATTAAGAGAGATCATAAAAACATCATAATAAGTCAAAAAAGAAAACAGGTTGAGCTCGTAAAATGTAGGTTTGCTGTATGTCAGCACACATTTAGTCTGTTCTTCCCTCTTTCAGA[T/A]AATCTGTGTAATGGGAAGTTTCACAAGCACCTGCAGGATCTGTTTGCTCCTCTGGTGGTGAGGTATGTGGATCTTATGGAGTCGTCCATCGCTCAGTCCATTCACAGAGGATTCGAACGAGAGTCTTGGGAGCCTGTCAAGTAAGCAGAACACTTCTTTGCTGATCAATCCAACACTGATTAAATGGGTGTTCTTCATTACTAAAACAACTAAAACTTAATCATGCTTATCCGCAGTCTCACTATTCACACACGCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACGCACACACACACACAGTAAAAGCATTTATTTATATGTTGTTGTTTGTTTGTGTGTGTGTGTGTGTGTGTGTGTTCAAAATTCAGAATTCAAAACAGAGTTTGAACAGCACTGGAACATGTTTCAGTTATTTTTTTATTGAGTTGTTTTACTTATTTTTAGTATTATTGTTATCGTTATTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14101
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 |
---|---|---|---|---|---|
ENSDART00000029680 | Nonsense | 1034 | 1316 | 23 | 30 |
Genomic Location (Zv9):
Chromosome 11 (position 20419477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 19836791 |
GRCz11 | 11 | 19999133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACYGTGTTCTGTGGTGWTTTCAGCAATGGTTCGGGGACGTCTGAAGAYT[T/A]GTTTTGGAAGCKGGACGCTCTGCAAACATTCATTAGAGACCTGCACTGGC
Long Flanking Sequence:
ATGCCTTGATGGCCTGCTGGCTGTTTGAGGACTTAGGCTGTAAGGAATAGTGCCAGAGTCAGTCTCTGCTTTTTACCATTTATTACAAAAGGATTGAATTTTTGATTGAATATCAGGGACCGTCTCTCCTCCTTCCACACACATTAACCTTAACATTGTGATCCTGCTGTTTTCCTTTGACAACATTGTGCATGTTTAACCTTCCCTGTTCTCAAACAACCAAAAGATTGTTTATACTATTTTGTTTCAGAGTTAACCCTTTATTTTTTCCATGGACTGATCAGCACAAACATCTGCAACGATCGGGAAGTGGTAAAAAATAACCAAACCAAATGTATGTGGACATGAAACAGTTTTTGTCTTCTTTAACAACCCGCCTTCCTCTGAGCTGTCCCGTATTCCTGACATTTTTGGGGCTGTCCTTTCCTGATTTACAGTTGTGGTTGAATAAACTGTGTTCTGTGGTGTTTTCAGCAATGGTTCGGGGACGTCTGAAGATT[T/A]GTTTTGGAAGCTGGACGCTCTGCAAACATTCATTAGAGACCTGCACTGGCCAGAAGAAGAGTTTGCCAAACATTTGGAGATGCGACTTAAACTCATGTCCAGTGATATGATCGAGTCCTGTGTTAAAAGGTGAGAACAGAACACACAAATACATATACATATACACTCACACTCACAGGCCACTTTATTAGGTACACCTTACTTGTACCGGGTTGGACCCCCTTTTGCCTTCACAACCACCTTAATCCTTATTGGCATAGATTCAACAAGGTACTGGAAATATTCCTCAGAGATGTTGGTCCATATTGACATGACAGCAGTTGCTGCAGATTTGCCAGCTGCACATCCATGATAGCCATCAGAAGATGGCTACACTAAGGTCATAAAGAGATGGATATGGTCAACAACAATACTCAGGTAGGCTGTGGTGTTGACATGATGCTCAATTAGTACTAATGGACCCAAAGTGTGCCAAGAAAATATCCCCTACACCATTACAC
Associated Phenotype:
Not determined