Gene Name HGNC ID COSMIC_MutID Primary sitePrimary histology AA-Mutation Mutation Type Genomic PositionFATHMM predictionFATHMM scoreLiterature evidence
MAPK76880COSM98930, stomachcarcinomap.E723KSubstitution - Missense17:19382816-19382816, PATHOGENIC0.9737121097718
MAPK76880COSM94671, lungcarcinomap.D809NSubstitution - Missense17:19383205-19383205, PATHOGENIC0.9587720668451
MAPK76880COSM48547, lungcarcinomap.G697RSubstitution - Missense17:19382392-19382392, NEUTRAL0.1092218948947
MAPK76880COSM94670, lungcarcinomap.P589SSubstitution - Missense17:19382068-19382068, NEUTRAL0.0575120668451
MAPK76880COSM87894, central_nervous_systemprimitive_neuroectodermal_tumour-medulloblastomap.A653fs*61Deletion - Frameshift17:19382259-19382259, Info_not_availableInfo_not_available21163964