Gene Name | HGNC ID | COSMIC_MutID | Primary site | Primary histology | AA-Mutation | Mutation Type | Genomic Position | FATHMM prediction | FATHMM score![]() | Literature evidence |
MAPK7 | 6880 | COSM98930, | stomach | carcinoma | p.E723K | Substitution - Missense | 17:19382816-19382816, | PATHOGENIC | 0.97371 | 21097718 |
MAPK7 | 6880 | COSM94671, | lung | carcinoma | p.D809N | Substitution - Missense | 17:19383205-19383205, | PATHOGENIC | 0.95877 | 20668451 |
MAPK7 | 6880 | COSM48547, | lung | carcinoma | p.G697R | Substitution - Missense | 17:19382392-19382392, | NEUTRAL | 0.10922 | 18948947 |
MAPK7 | 6880 | COSM94670, | lung | carcinoma | p.P589S | Substitution - Missense | 17:19382068-19382068, | NEUTRAL | 0.05751 | 20668451 |
MAPK7 | 6880 | COSM87894, | central_nervous_system | primitive_neuroectodermal_tumour-medulloblastoma | p.A653fs*61 | Deletion - Frameshift | 17:19382259-19382259, | Info_not_available | Info_not_available | 21163964 |