Gene Name HGNC ID COSMIC_MutID Primary sitePrimary histology AA-Mutation Mutation Type Genomic PositionFATHMM predictionFATHMM scoreLiterature evidence
PFKFB38874COSM40459, central_nervous_systemgliomap.A78TSubstitution - Missense10:6215250-6215250, PATHOGENIC0.9783518772396
PFKFB38874COSM314096, lungcarcinomap.K451RSubstitution - Missense10:6226202-6226202, PATHOGENIC0.7698222941188
PFKFB38874COSM5027177, breastcarcinomap.V17VSubstitution - coding silent10:6203311-6203311, NEUTRAL0.0416122722193