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ACAATAAATAAATCACCAGAAAATA[C/T]GTTTCTACCTAAACATTCCATTATC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603196 MIM: 614766 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
COCH PubMed Links | |||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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COCH - cochlin | ||||||
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There are no transcripts associated with this gene. |
LOC100506071 - uncharacterized LOC100506071 | ||||||
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There are no transcripts associated with this gene. |
STRN3 - striatin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001083893.1 | Intron | NP_001077362.1 | ||||
NM_014574.3 | Intron | NP_055389.3 | ||||
XM_005267569.3 | Intron | XP_005267626.1 | ||||
XM_005267570.3 | Intron | XP_005267627.1 |