Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_020695.3 | 3797 | Silent Mutation | AGC,AGT | S1199S | NP_065746.3 |
XM_011528144.1 | 3797 | Nonsense Mutation | CGA,TGA | R1232* | XP_011526446.1 |
XM_011528146.2 | 3797 | Nonsense Mutation | CGA,TGA | R1197* | XP_011526448.1 |
XM_017027028.1 | 3797 | Nonsense Mutation | CGA,TGA | R1223* | XP_016882517.1 |
XM_017027029.1 | 3797 | Silent Mutation | AGC,AGT | S1208S | XP_016882518.1 |
XM_017027030.1 | 3797 | Intron | XP_016882519.1 |