Gene Name HGNC ID COSMIC_MutID Primary sitePrimary histology AA-Mutation Mutation Type Genomic PositionFATHMM predictionFATHMM scoreLiterature evidence
ACLY115COSM39766, central_nervous_systemgliomap.S525ASubstitution - Missense17:41893061-41893061, PATHOGENIC0.994718772396
ACLY115COSM3717363, livercarcinomap.A1000VSubstitution - Missense17:41869526-41869526, PATHOGENIC0.96964Info_not_available
ACLY115COSM5028298, breastcarcinomap.F197FSubstitution - coding silent17:41909014-41909014, PATHOGENIC0.9356422722193
ACLY115COSM1610253, livercarcinomap.A1000SSubstitution - Missense17:41869527-41869527, PATHOGENIC0.86505Info_not_available