Gene Name HGNC ID COSMIC_MutID Primary sitePrimary histology AA-Mutation Mutation Type Genomic PositionFATHMM predictionFATHMM scoreLiterature evidence
PPM1J20785COSM95039, breastcarcinomap.W431LSubstitution - Missense1:112710538-112710538, PATHOGENIC0.9893120668451
PPM1J20785COSM5047063, oesophaguscarcinomap.L173MSubstitution - Missense1:112712956-112712956, PATHOGENIC0.9876724686850
PPM1J20785COSM5049264, oesophaguscarcinomap.R329KSubstitution - Missense1:112711326-112711326, PATHOGENIC0.9866424686850
PPM1J20785COSM96142, breastcarcinomap.T204TSubstitution - coding silent1:112712861-112712861, NEUTRAL0.2008820668451
PPM1J20785COSM40497, central_nervous_systemgliomap.R372RSubstitution - coding silent1:112710846-112710846, NEUTRAL0.1022318772396
PPM1J20785COSM314377, lungcarcinomap.G163GSubstitution - coding silent1:112712984-112712984, NEUTRAL0.036822941188