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TCCTGGTCCCAGATGGGAACCCGCA[A/G]GTCCAGCCAGTCATTCCGCACCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603189 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC105369332 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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LOC105369332 - uncharacterized LOC105369332 | ||||||
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There are no transcripts associated with this gene. |
RNU2-2P - RNA, U2 small nuclear 2, pseudogene | ||||||
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There are no transcripts associated with this gene. |
STX5 - syntaxin 5 | ||||||
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There are no transcripts associated with this gene. |
WDR74 - WD repeat domain 74 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001307977.1 | 627 | Silent Mutation | CTG,TTG | L,L 180 | NP_001294906.1 | |
NM_018093.3 | 627 | Silent Mutation | CTG,TTG | L,L 180 | NP_060563.2 | |
XM_005274055.2 | 627 | Silent Mutation | CTG,TTG | L,L 180 | XP_005274112.1 |
Set Membership: |
HapMap |