ZMP
wdr33
Ensembl ID:
ZFIN ID:
Description:
WD repeat domain 33 (wdr33), transcript variant 2, mRNA [Source:RefSeq DNA;Acc:NM_001024221]
Human Orthologue:
WDR33
Human Description:
WD repeat domain 33 [Source:HGNC Symbol;Acc:25651]
Mouse Orthologue:
Wdr33
Mouse Description:
WD repeat domain 33 Gene [Source:MGI Symbol;Acc:MGI:1921570]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13555 | Nonsense | Available for shipment | Available now |
sa15874 | Nonsense | Available for shipment | Available now |
sa39759 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7527 | Missense | Mutation detected in F1 DNA | Not yet available |
sa32835 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31252 | Nonsense | Available for shipment | Available now |
sa39758 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13555
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025131 | Nonsense | 27 | 1164 | 1 | 25 |
ENSDART00000124113 | Nonsense | 27 | 557 | 2 | 15 |
ENSDART00000138885 | Nonsense | 14 | 992 | 2 | 19 |
ENSDART00000025131 | Nonsense | 27 | 1164 | 1 | 25 |
ENSDART00000124113 | Nonsense | 27 | 557 | 2 | 15 |
ENSDART00000138885 | Nonsense | 14 | 992 | 2 | 19 |
The following transcripts of ENSDARG00000018272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 5080241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5525969 |
GRCz11 | 2 | 5437851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTCCAYATGCCTCGCTTCCAGCACCAGGCTCYCCGWCAGCTGTTCTA[C/A]AAGAGGCCCGACTTCGCCCAGCAGCAGGCCATGCAGCAGCTCACCTTCGA
Long Flanking Sequence:
TTGGTTTATTCCTGCAAAAAAAAGTCCTGGAAAGCTATTTTGATCCATTGCAGTTCAACTGAAAGAACATATTAGCATAACCTGTGTAACACTTACTTGGTTACTTGCATAATAAAATGAGAAAAATGGTTCTTATTTAAAGATGGTGGTTTAAGTTGTCGATAACCTTGTGTATTGATTTGTAGTATTGTACTTACCCCCCGCCCCCCAAAGAGTGTTGTTGTCTATGCCCAAATTTTTCAATCACACAATCACATACATTTCTAAAATGAATCCGTGTCATTAACCATGGTTTTTTTTGCCTATGTGTTGTTGTTTTGCATTGATCTGTGCATTTAGTTGCTGATGTTCTCTTGAATTTAGCCAGCGGAAAGAACCCTTAATTTCTCTCCATATCCTCAGGTGTACTAAACCGTGACCATGGCGACTGACATCGGCTCCCCTCCGCGGTTCTTCCATATGCCTCGCTTCCAGCACCAGGCTCCCCGTCAGCTGTTCTA[C/A]AAGAGGCCCGACTTCGCCCAGCAGCAGGCCATGCAGCAGCTCACCTTCGACGGCAAGCGCATGAGAAAAGCCGTCAACCGCAAAACCATCGATTACAATCCATCCGTCATCAGACATCTAGAGGTATTAGCCTAGCAGAAATACAACTCTCTTTTTTATTGTATGTATTTATTTGGTATAGTTCTGCTTTCACCTCACCCTACAGTTTTTTTTCCTGTAACTTGTTAAGTTTGATTTGTATTGTAAGAATATATTTACTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATCCGCTGCATAAAACATTCTGGATAAGTTGGCGGTTCATTCTGCTGTAGCGACCCCTTATTAATAAAGGGACTAAGCAAATAAGAAAATGAATGAATATATTTACATGTTTGCACTGAGTAAGATGCACTTAGTCTTGTCGCACATGTATATAATGTACCATCTATATCTGTACAGTTACAATAAAAGCCATTCTATTAGGTTAGTGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15874
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025131 | Nonsense | 27 | 1164 | 1 | 25 |
ENSDART00000124113 | Nonsense | 27 | 557 | 2 | 15 |
ENSDART00000138885 | Nonsense | 14 | 992 | 2 | 19 |
ENSDART00000025131 | Nonsense | 27 | 1164 | 1 | 25 |
ENSDART00000124113 | Nonsense | 27 | 557 | 2 | 15 |
ENSDART00000138885 | Nonsense | 14 | 992 | 2 | 19 |
The following transcripts of ENSDARG00000018272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 5080241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5525969 |
GRCz11 | 2 | 5437851 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTCCAYATGCCTCGCTTCCAGCACCAGGCTCYCCGWCAGCTGTTCTA[C/A]AAGAGGCCCGACTTCGCCCAGCAGCAGGCCATGCAGCAGCTCACCTTYGA
Long Flanking Sequence:
TTGGTTTATTCCTGCAAAAAAAAGTCCTGGAAAGCTATTTTGATCCATTGCAGTTCAACTGAAAGAACATATTAGCATAACCTGTGTAACACTTACTTGGTTACTTGCATAATAAAATGAGAAAAATGGTTCTTATTTAAAGATGGTGGTTTAAGTTGTCGATAACCTTGTGTATTGATTTGTAGTATTGTACTTACCCCCCGCCCCCCAAAGAGTGTTGTTGTCTATGCCCAAATTTTTCAATCACACAATCACATACATTTCTAAAATGAATCCGTGTCATTAACCATGGTTTTTTTTGCCTATGTGTTGTTGTTTTGCATTGATCTGTGCATTTAGTTGCTGATGTTCTCTTGAATTTAGCCAGCGGAAAGAACCCTTAATTTCTCTCCATATCCTCAGGTGTACTAAACCGTGACCATGGCGACTGACATCGGCTCCCCTCCGCGGTTCTTCCATATGCCTCGCTTCCAGCACCAGGCTCCCCGTCAGCTGTTCTA[C/A]AAGAGGCCCGACTTCGCCCAGCAGCAGGCCATGCAGCAGCTCACCTTCGACGGCAAGCGCATGAGAAAAGCCGTCAACCGCAAAACCATCGATTACAATCCATCCGTCATCAGACATCTAGAGGTATTAGCCTAGCAGAAATACAACTCTCTTTTTTATTGTATGTATTTATTTGGTATAGTTCTGCTTTCACCTCACCCTACAGTTTTTTTTCCTGTAACTTGTTAAGTTTGATTTGTATTGTAAGAATATATTTACTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATCCGCTGCATAAAACATTCTGGATAAGTTGGCGGTTCATTCTGCTGTAGCGACCCCTTATTAATAAAGGGACTAAGCAAATAAGAAAATGAATGAATATATTTACATGTTTGCACTGAGTAAGATGCACTTAGTCTTGTCGCACATGTATATAATGTACCATCTATATCTGTACAGTTACAATAAAAGCCATTCTATTAGGTTAGTGCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39759
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 |
---|---|---|---|---|---|
ENSDART00000025131 | Essential Splice Site | 91 | 1164 | None | 25 |
ENSDART00000124113 | Essential Splice Site | 91 | 557 | None | 15 |
ENSDART00000138885 | Essential Splice Site | 78 | 992 | None | 19 |
The following transcripts of ENSDARG00000018272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 5079530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5525258 |
GRCz11 | 2 | 5437140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCGAGATTTCCGTGCTGTTCAACCAGACGCAGGCTGCTATAATGAAG[T/A]GAGTGTTTTACTACTACTGCTGCTATTTACAGTTATTGTGCGTGTTTTTT
Long Flanking Sequence:
TTTCCTGTAACTTGTTAAGTTTGATTTGTATTGTAAGAATATATTTACTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATCCGCTGCATAAAACATTCTGGATAAGTTGGCGGTTCATTCTGCTGTAGCGACCCCTTATTAATAAAGGGACTAAGCAAATAAGAAAATGAATGAATATATTTACATGTTTGCACTGAGTAAGATGCACTTAGTCTTGTCGCACATGTATATAATGTACCATCTATATCTGTACAGTTACAATAAAAGCCATTCTATTAGGTTAGTGCTCTTCATTTGATATGCATTTGCATGTGTTGCTAATAAGGAAATCAATAAAAAAGTTAAAATCATAAAGAAATGCATCTCACTGTAAACCAAGCCCTCTTCCTCTGCCACTTTTAACACTTTTCAAATGACTCCCTTTTTCAGAATCGATTGTGGCAGCGAGATCATCGAGATTTCCGTGCTGTTCAACCAGACGCAGGCTGCTATAATGAAG[T/A]GAGTGTTTTACTACTACTGCTGCTATTTACAGTTATTGTGCGTGTTTTTTCAGTTTATATCACTAATAAAATAATCACTTTTCTTGTAGCTCGTTCCCCCAGTGGGCATGATTAGCAATCCTATGAATGCTGTCACGACAAAGTTTGTCAGAACCTCCACCAACAAAGTCAAATGCCCTGTGTTTGTTGTGAGGGTAAGTGTTATAAGAAATACATTTTGCTGTAAAACTAATGCAGTCTCACTGCGATTCATAACATTTTTTTTTATTTAAATTCGTATTAATTTTTATTATCTCATTCATATATTTTTTGTATGATTTGCACATCCCCCAATGAGGGGTGGGAATTGGCGCTATTTTTTTTATTATTATTAAAAATTGTATGAATGAAGGGTTCATACTGTCCTGGAAAAGTCCATGGAATTTTCCCCTGCCTGAAAAGTTTTAAAAAAACCAATAAACCTAAAATGTTTTGGTAAAGTCATGGAAGTGTTTAACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7527
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 > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025131 | Missense | 151 | 1164 | 4 | 25 |
ENSDART00000124113 | Missense | 151 | 557 | 5 | 15 |
ENSDART00000138885 | Missense | 138 | 992 | 5 | 19 |
The following transcripts of ENSDARG00000018272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 5077870)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5523598 |
GRCz11 | 2 | 5435480 |
KASP Assay ID:
554-4298.1 (used for ordering genotyping assays)
KASP Sequence:
TTGTAACAGGTGCCTCCAGTGGGGAGTTTACTTTATGGAAYGGGCTCACG[T/G]TCAACTTTGAGACAATTTTACAGGTAACCATAGAGAGACAYAACCTGTTC
Long Flanking Sequence:
TTTACTTAGCAACACAATAATTTAGCAAATAAACAAACGTAAATGTTATCCTGCTTGTTTTTGAGGTGGTGTCGAGCGAGTTCTTTAATGCCTTTGATAGGTCACGCGCTCAACGGAAAGGGCTGCGATTGGCTCTAACGCTCTGGTGATGTTCACCGACAAGTGACACTGATATATACGGACGGAGCAATCACAGCTGATCCATGATAGACGTGGTGAAGAAAACCTGCTCTGCAGACACGCTCGTGTCTGGATCAACAAGTTTCTCTATAACAGCCAAGAGGAGATTAGTTTTGACACCACTAGTATCAACCCTGTCCTACGAATTAGCCACTTGAATAGATCTAAAATAGTTAAATTCGACATGAAATCAGGCTTATAAAACCCCATGTACTAAATGTCTGTGTCCTTTTCTTCCTTTTTTATAGTGGACTCCTGAAGGCAGGCGACTTGTAACAGGTGCCTCCAGTGGGGAGTTTACTTTATGGAATGGGCTCACG[T/G]TCAACTTTGAGACAATTTTACAGGTAACCATAGAGAGACACAACCTGTTCATAACCTCAAAAGCTTGCTCAAAGTCCGTTATTTATTTATCCATGTTTCTTTCCTTTTTATAGGCTCATGACAGCCCTGTCAGGGCAATGACCTGGTCTCATAATGACATGTGGATGTTAACTGCCGACCATGGAGGTTATGTGAAGTACTGGCAGTCCAACATGAATAACGTCAAGATGTTCCAGGCTCACAAGGAGGCGATTAGAGAGGCCAGGTCTATACACAATCTACCATTTTCTGTAGTTAACCCAAGCCTGTTACTGCTCCTGCAGTGGCAGGGCTCTGCCTGTAGGGGGCTCTCCTCAGTGCTGATATATTCTTCCCTGTGCTGCTCAATGTTCATGTCCTTTTTGATTGATACGTGTGTTTATTTGTCACCTGTGGCTGAGTTATGTATCCTCATCTTTTATATACATAGCTACTTTGTACAGAAAAGGTGTATTTTTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32835
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025131 | Nonsense | 549 | 1164 | 14 | 25 |
ENSDART00000124113 | Nonsense | 549 | 557 | 15 | 15 |
ENSDART00000138885 | Nonsense | 536 | 992 | 15 | 19 |
The following transcripts of ENSDARG00000018272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 5065004)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5510732 |
GRCz11 | 2 | 5422614 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGCAAGAAGAAGACGCAAGCAGAGATTGAGCAGGAAATGGCTGCCCTG[C/T]AGTATACAAACCCAATGCTGCTCGAGGTCAGCAAATGTGCTACTTAAAAA
Long Flanking Sequence:
GAAGGCAGCCATGGAACAAGAACAATCAGGTTGGGAAACACATTCAGTTACAGTAATGTTCATTTATATTATATTCATGCATTGATAGTTTAATGGTTTATCGATGTTGATGTGCCTAGGGAAAGACATGGTGGCAGAGCCTGAGATGAGCATCCCGGGGCTGGACTGGGGCATGGAAGAGGTCATGCTGAGGGACCAAAAAAAGGCCCCGACTAAAAAAGTTCCTTATGCAAAACCCATTCCAGCTCAGTTCCAACAGGTCAGTTAGATAACTCGGTGTATGGTTTGGTGTCACTGCCAGATTTATTGTGTTTTTGCTTTTATGGATAAGTTATACATTAGTTACATGTTACTTTTAATTGAATTCAATTCAGGCCTGGGCAGAGAATAAGGTTCCGGTGATGCCTGCTGGAGAAGTTCCAAAGGAAAGGAAGGATGAGAAGAAAGTAGATAGCAAGAAGAAGACGCAAGCAGAGATTGAGCAGGAAATGGCTGCCCTG[C/T]AGTATACAAACCCAATGCTGCTCGAGGTCAGCAAATGTGCTACTTAAAAAAATGTCAATAATCACTGTATTGTGAATATGAACAATAAGAAAATTCTTTGTTTGTCAACAGCAACTGAAGATTGAGCGAATGGCACAGTTGCAGGAGCAGGGACTTCCTCCCCCTACTGGACAGCAGTCAGGACCAGTTCCGTCCTTTCCAGGGCAAGGTGGTCCAATGCCTCCTCCAGCACAAGGCTTCCCTCAGTCCATGCCTCCACAGCAAACACCACACAACATGCCTCCTGTTGGACCAGGGGGGATGCCTGGTCCATTCATACCTTCAGGCCAAATGGGCCCACCGGGACCTCCCATGCACCAGGGTCCGCCTCCACAGGGCATGATGGGACCTCCAGACATGCATGGACCTCCACGTCATCCCGGCCCTCACAGGAACATTGGACCCCAGGGTCCTCCTGGCATGCCGCCAGGCCCCAGAGGCATGCAAGGACCTCCCCCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31252
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 |
---|---|---|---|---|---|
ENSDART00000025131 | Nonsense | 708 | 1164 | 15 | 25 |
ENSDART00000124113 | None | None | 557 | None | 15 |
ENSDART00000138885 | Nonsense | 695 | 992 | 16 | 19 |
The following transcripts of ENSDARG00000018272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 5064442)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5510170 |
GRCz11 | 2 | 5422052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCTCTGGTGGACCTCCAGGCAGTATTATGGGACCACCGCCACGAGGA[C/T]AGGGTCCTCCACAAGGAAATATGATGCATCAGGACATGAGGGGGCCTGTG
Long Flanking Sequence:
TCACTGTATTGTGAATATGAACAATAAGAAAATTCTTTGTTTGTCAACAGCAACTGAAGATTGAGCGAATGGCACAGTTGCAGGAGCAGGGACTTCCTCCCCCTACTGGACAGCAGTCAGGACCAGTTCCGTCCTTTCCAGGGCAAGGTGGTCCAATGCCTCCTCCAGCACAAGGCTTCCCTCAGTCCATGCCTCCACAGCAAACACCACACAACATGCCTCCTGTTGGACCAGGGGGGATGCCTGGTCCATTCATACCTTCAGGCCAAATGGGCCCACCGGGACCTCCCATGCACCAGGGTCCGCCTCCACAGGGCATGATGGGACCTCCAGACATGCATGGACCTCCACGTCATCCCGGCCCTCACAGGAACATTGGACCCCAGGGTCCTCCTGGCATGCCGCCAGGCCCCAGAGGCATGCAAGGACCTCCCCCAGGAGGGATGCACCCTGGCTCTGGTGGACCTCCAGGCAGTATTATGGGACCACCGCCACGAGGA[C/T]AGGGTCCTCCACAAGGAAATATGATGCATCAGGACATGAGGGGGCCTGTGCCCCATGGAAACATGATGGGCCCTCAGGGACCCATGCAAGGGGGTATGATGGGCCCTCCGCTCAGGACTCATGGCATGGGAAATATGCATGGGATGGGACCTCCTCCTGGGGGTATGCATGGACCACCAAACAACATGCAAGGGCCACCAGGAAATATACAAGGACCTCAAAGCAGCATGCAGGGCCCCCCACCATATATGCAGGGCAAACCCCCACACATGGGTGATGGAAATCGAGGACAGTTCAGCCAGGTGATTATTCCTTACACCCATGAATGTTAAAAGGGTCACGAAACACCAAAACACATTTTTTGAGCTGTTGACAGTCGTATATGTGTCCCATTCTGCTAAAAACACTATTAGGACACCTATATTTCACTAAAAAGTGTAAATTGGTTGTTTTTGCGTTATTTCAAGCAAATTCGTACTTCCTGTTTGAAACGAATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39758
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025131 | Nonsense | 823 | 1164 | 16 | 25 |
ENSDART00000124113 | None | None | 557 | None | 15 |
ENSDART00000138885 | Nonsense | 803 | 992 | 17 | 19 |
The following transcripts of ENSDARG00000018272 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 5062812)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5508540 |
GRCz11 | 2 | 5420422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCACATGTGTTCCAGGGTCAGAATCAGCCAATCATGCATGGAATAGGA[C/T]AGCAGGGTCCTAACGGAAAAGGTAATGCTCTGAATAGTGAATGCTTCAGT
Long Flanking Sequence:
TGTGCATCTAAGTTTCCGGGAAATGCTGAGTTTTTTTTCTCTCATTCGCCGTGCGGGATCAAACATTGCATGAAAAATACACGCTTAGAGCAGTTCCTCAAATCAAATATCACGTTTGTCGGGAGGGACATGAATGAATTCCCTGAATGAAAGAGCCAAACTGCAGTTAAAGTCCAACATTTAATAATTTGGCAAATAATTCGACTACATATGTCCATGTAAACACAGTCACATTGTCCGCTGTGGGTGTGTGTTTTGACTCTGAAATTCAGCGCGCCCAAATAGACACTCCCATACCAAGCCTCTTTTCTTCCTCCGACACTCCCCCCTAAACAGAGCTGGACACGCCCACTTTTCTGACTTTTTCCAAAGTAGAGGTGTGAAAACACACTGCTGAAACGAGGGGGTTTCATGGCCCTTTAAGACAAAGTAGCTTCCATTGCTGAACTGTTTCACATGTGTTCCAGGGTCAGAATCAGCCAATCATGCATGGAATAGGA[C/T]AGCAGGGTCCTAACGGAAAAGGTAATGCTCTGAATAGTGAATGCTTCAGTGTTGATCTTATGCAAAGTGATTTAATCGTGACATTTGACCCCTTTCGCTGTCTATGTCAGATGGTTCACGAGGGCCACCTAACCACCACATGGCTCACCCACCAGAGCGACAAGGCCCCGGAGGACCTAGTCAGAGCTCAGACGGAGGCCAGTACTGGGGGGAAGATGGGGGTTACCAAGAGGGCTGGAGAAGAGGCCCTGGAGGTCCTGCACAGGAATACTCTGGAGGTCACAGAGGAAACTCTGGAGGCCAGTGGGAAGGCCAGGAAAGGTTTTCCACACGTGATGAAGAGTTCATGGGGTATGTTTCATTCATCATGACTGCATTTCACTCCACTTTTACACATTTTGAAGTGTGTTCCACTTCATCAAATGAACAAGGGAAGGATTATATGGACATACCCTTGACCTCTTAAATTTGAGCAAGGGTTCTTCACATGTCCACTCCAG
Associated Phenotype:
Not determined