HapMap
Validated
HapMap
Validated
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001040428.3 | 150 | Missense Mutation | AAT,GAT | N2D | NP_001035518.1 |
| NM_018418.4 | 150 | Missense Mutation | AAT,GAT | N2D | NP_060888.2 |
| XM_005267851.1 | 150 | Missense Mutation | AAT,GAT | N2D | XP_005267908.1 |
| XM_005267852.1 | 150 | Missense Mutation | AAT,GAT | N2D | XP_005267909.1 |
| XM_005267854.1 | 150 | UTR 5 | XP_005267911.1 | ||
| XM_005267855.1 | 150 | UTR 5 | XP_005267912.1 | ||
| XM_006720204.1 | 150 | Missense Mutation | AAT,GAT | N2D | XP_006720267.1 |
| XM_006720205.1 | 150 | Missense Mutation | AAT,GAT | N2D | XP_006720268.1 |
| XM_011536951.1 | 150 | UTR 5 | XP_011535253.1 | ||
| XM_011536952.1 | 150 | Missense Mutation | AAT,GAT | N2D | XP_011535254.1 |
| XM_011536953.1 | 150 | UTR 5 | XP_011535255.1 | ||
| XM_017021452.1 | 150 | UTR 5 | XP_016876941.1 | ||
| XM_017021453.1 | 150 | UTR 5 | XP_016876942.1 | ||
| XM_017021454.1 | 150 | UTR 5 | XP_016876943.1 | ||
| XM_017021455.1 | 150 | UTR 5 | XP_016876944.1 | ||
| XM_017021456.1 | 150 | Intron | XP_016876945.1 | ||
| XM_017021457.1 | 150 | UTR 5 | XP_016876946.1 |