Gene Name HGNC ID COSMIC_MutID Primary sitePrimary histology AA-Mutation Mutation Type Genomic PositionFATHMM predictionFATHMM scoreLiterature evidence
CTDP12498COSM4767511, biliary_tractcarcinomap.R772WSubstitution - Missense18:79717913-79717913, PATHOGENIC0.9826524997986
CTDP12498COSM310385, lungcarcinomap.P627LSubstitution - Missense18:79715340-79715340, PATHOGENIC0.9718422941188
CTDP12498COSM310386, lungcarcinomap.R933WSubstitution - Missense18:79753701-79753701, PATHOGENIC0.9012622941188
CTDP12498COSM196285, biliary_tractcarcinomap.A331ASubstitution - coding silent18:79713101-79713101, NEUTRAL0.0119224997986