HapMap
HapMap
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039970.1 | 3183 | UTR 3 | NP_001035059.1 | ||
| NM_001278236.1 | 3183 | UTR 3 | NP_001265165.1 | ||
| NM_001278238.1 | 3183 | UTR 3 | NP_001265167.1 | ||
| NM_001278239.1 | 3183 | UTR 3 | NP_001265168.1 | ||
| NM_006906.1 | 3183 | UTR 3 | NP_008837.1 | ||
| NM_032781.3 | 3183 | UTR 3 | NP_116170.3 | ||
| XM_011520411.2 | 3183 | UTR 3 | XP_011518713.1 | ||
| XM_017018434.1 | 3183 | Missense Mutation | CCT,CGT | P618R | XP_016873923.1 |
| XM_017018435.1 | 3183 | Missense Mutation | CCT,CGT | P618R | XP_016873924.1 |
| XM_017018436.1 | 3183 | Missense Mutation | CCT,CGT | P594R | XP_016873925.1 |
| XM_017018437.1 | 3183 | Missense Mutation | CCT,CGT | P586R | XP_016873926.1 |
| XM_017018438.1 | 3183 | Missense Mutation | CCT,CGT | P579R | XP_016873927.1 |
| XM_017018439.1 | 3183 | Missense Mutation | CCT,CGT | P562R | XP_016873928.1 |
| XM_017018440.1 | 3183 | UTR 3 | XP_016873929.1 | ||
| XM_017018441.1 | 3183 | Intron | XP_016873930.1 |