Gene Name HGNC ID COSMIC_MutID Primary sitePrimary histology AA-Mutation Mutation Type Genomic PositionFATHMM predictionFATHMM scoreLiterature evidence
PRKD19407COSM2034048, oesophaguscarcinomap.G599ESubstitution - Missense14:29626486-29626486, PATHOGENIC0.9906324686850
PRKD19407COSM314445, lungcarcinomap.R740LSubstitution - Missense14:29597706-29597706, PATHOGENIC0.9903322941188
PRKD19407COSM33112, large_intestinecarcinomap.H152YSubstitution - Missense14:29666158-29666158, PATHOGENIC0.9892116959974
PRKD19407COSM5049611, oesophaguscarcinomap.P146SSubstitution - Missense14:29666176-29666176, PATHOGENIC0.9892124686850
PRKD19407COSM32282, large_intestinecarcinomap.E857KSubstitution - Missense14:29577408-29577408, PATHOGENIC0.9885816959974
PRKD19407COSM48700, lungcarcinomap.V743LSubstitution - Missense14:29597698-29597698, PATHOGENIC0.9866918948947
PRKD19407COSM5046767, oesophaguscarcinomap.D359NSubstitution - Missense14:29636405-29636405, PATHOGENIC0.9844424686850
PRKD19407COSM20976, lungcarcinomap.R677MSubstitution - Missense14:29599693-29599693, PATHOGENIC0.9798216140923
PRKD19407COSM20976, lungcarcinomap.R677MSubstitution - Missense14:29599693-29599693, PATHOGENIC0.97982Info_not_available
PRKD19407COSM20976, lungcarcinomap.R677MSubstitution - Missense14:29599693-29599693, PATHOGENIC0.97982Info_not_available
PRKD19407COSM20976, lungcarcinomap.R677MSubstitution - Missense14:29599693-29599693, PATHOGENIC0.9798216140923
PRKD19407COSM1607591, livercarcinomap.H152RSubstitution - Missense14:29666157-29666157, PATHOGENIC0.97837Info_not_available
PRKD19407COSM314447, lungcarcinomap.G856GSubstitution - coding silent14:29577409-29577409, PATHOGENIC0.8104222941188
PRKD19407COSM1607593, livercarcinomap.V117MSubstitution - Missense14:29725590-29725590, Info_not_available0.69871Info_not_available
PRKD19407COSM5048325, oesophaguscarcinomap.S50ASubstitution - Missense14:29927365-29927365, Info_not_available0.6654224686850