Cancer | Mutation Type | UniProtKB | Location | Mutation | PDB Res | FunFam | Links | View |
---|---|---|---|---|---|---|---|---|
LUAD | Missense Mutation | Q14191 | Q→H | 2dgz:A:1165 |
Werner syndrome ATP-dependent helicase 1.10.150.80-FF-3214 |
UniProtKB InterPro | GO | |
LUAD | Missense Mutation | Q14191 | Q→H | 2dgz:A:1165 |
Werner syndrome ATP-dependent helicase 1.10.150.80-FF-3214 |
UniProtKB InterPro | GO | |
SKCM | Missense Mutation | Q14191 | S→F | 2fbt:A:194 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
SKCM | Missense Mutation | Q14191 | S→F | 2fbt:A:194 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
PAAD | Missense Mutation | Q14191 | R→C | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
PAAD | Missense Mutation | Q14191 | R→C | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
UCEC | Missense Mutation | Q14191 | S→R | 2fbt:A:198 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
UCEC | Missense Mutation | Q14191 | S→R | 2fbt:A:198 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO |