Cancer | Mutation Type | UniProtKB | Location | Mutation | PDB Res | FunFam | Links | View |
---|---|---|---|---|---|---|---|---|
CESC | Missense Mutation | Q9NVH0 | R→C | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
CESC | Missense Mutation | Q9NVH0 | R→C | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
HNSC | Missense Mutation | Q9NVH0 | R→C | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
HNSC | Missense Mutation | Q9NVH0 | R→C | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
LUAD | Missense Mutation | Q9NVH0 | R→G | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
LUAD | Missense Mutation | Q9NVH0 | R→G | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
SKCM | Missense Mutation | Q9NVH0 | R→C | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
SKCM | Missense Mutation | Q9NVH0 | R→C | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
SKCM | Missense Mutation | Q9NVH0 | R→C | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO | |
SKCM | Missense Mutation | Q9NVH0 | R→C | 2fbt:A:196 |
Werner syndrome ATP-dependent helicase 3.30.420.10-FF-45955 |
UniProtKB InterPro | GO |