Gene Name HGNC ID COSMIC_MutID Primary sitePrimary histology AA-Mutation Mutation Type Genomic PositionFATHMM predictionFATHMM scoreLiterature evidence
MAPK86881COSM99080, stomachcarcinomap.E247*Substitution - Nonsense10:48425938-48425938, PATHOGENIC0.9946321097718
MAPK86881COSM20763, kidneycarcinomap.G171SSubstitution - Missense10:48420215-48420215, PATHOGENIC0.9898520054297
MAPK86881COSM20763, kidneycarcinomap.G171SSubstitution - Missense10:48420215-48420215, PATHOGENIC0.9898520054297
MAPK86881COSM13337, central_nervous_systemgliomap.G177RSubstitution - Missense10:48420233-48420233, PATHOGENIC0.9848416618716
MAPK86881COSM13337, central_nervous_systemgliomap.G177RSubstitution - Missense10:48420233-48420233, PATHOGENIC0.9848416618716
MAPK86881COSM94672, lungcarcinomap.S144FSubstitution - Missense10:48410149-48410149, PATHOGENIC0.9814520668451
MAPK86881COSM48880, lungcarcinomap.Q120*Substitution - Nonsense10:48410076-48410076, PATHOGENIC0.9812418948947