Gene NameHGNC IDCOSMIC_MutIDPrimary sitePrimary histologyAA-MutationMutation TypeGenomic PositionFATHMM predictionFATHMM scoreLiterature evidence
ALPL438COSM39830, central_nervous_systemgliomap.Y117YSubstitution - coding silent1:21563163-21563163, PATHOGENIC0.8940518772396
ALPL438COSM39829, central_nervous_systemgliomap.L471LSubstitution - coding silent1:21577484-21577484, PATHOGENIC0.8818718772396