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GTCCAGGCTCCACGCTGGGGCAACC[C/G]CCGTGCGCTCAGCTTCGTACTGAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 164350 MIM: 612159 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
OAS1 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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OAS1 - 2'-5'-oligoadenylate synthetase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001032409.2 | 476 | Missense Mutation | CCC,CGC | P,R 129 | NP_001027581.1 | |
NM_001320151.1 | 476 | Missense Mutation | CCC,CGC | P,R 129 | NP_001307080.1 | |
NM_002534.3 | 476 | Missense Mutation | CCC,CGC | P,R 129 | NP_002525.2 | |
NM_016816.3 | 476 | Missense Mutation | CCC,CGC | P,R 129 | NP_058132.2 | |
XM_006719434.1 | 476 | Missense Mutation | CCC,CGC | P,R 129 | XP_006719497.1 | |
XM_011538413.1 | 476 | Missense Mutation | CCC,CGC | P,R 129 | XP_011536715.1 | |
XM_017019361.1 | 476 | Missense Mutation | CCC,CGC | P,R 129 | XP_016874850.1 | |
XM_017019362.1 | 476 | UTR 5 | XP_016874851.1 |
RPH3A - rabphilin 3A | ||||||
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There are no transcripts associated with this gene. |