Gene Name HGNC ID COSMIC_MutID Primary sitePrimary histology AA-Mutation Mutation Type Genomic PositionFATHMM predictionFATHMM scoreLiterature evidence
PTPRF9670COSM4605137, upper_aerodigestive_tractcarcinomap.D1098ASubstitution - Missense1:43605347-43605347, PATHOGENIC0.9971725056374
PTPRF9670COSM4605137, upper_aerodigestive_tractcarcinomap.D1098ASubstitution - Missense1:43605347-43605347, PATHOGENIC0.9971725056374
PTPRF9670COSM6848004, pleuramesotheliomap.Y1405CSubstitution - Missense1:43617754-43617754, PATHOGENIC0.9955126928227
PTPRF9670COSM6848006, pleuramesotheliomap.P1292LSubstitution - Missense1:43609400-43609400, PATHOGENIC0.9951526928227
PTPRF9670COSM1581562, haematopoietic_and_lymphoid_tissuelymphoid_neoplasmp.V1636MSubstitution - Missense1:43619547-43619547, PATHOGENIC0.9597623292937
PTPRF9670COSM4604924, upper_aerodigestive_tractcarcinomap.I889MSubstitution - Missense1:43603819-43603819, PATHOGENIC0.9574925056374
PTPRF9670COSM40517, central_nervous_systemgliomap.W683*Substitution - Nonsense1:43597983-43597983, PATHOGENIC0.9102918772396
PTPRF9670COSM4605451, upper_aerodigestive_tractcarcinomap.E1571ESubstitution - coding silent1:43619354-43619354, PATHOGENIC0.8823325056374
PTPRF9670COSM27006, kidneyrenal_cell_carcinomap.R1182HSubstitution - Missense1:43606301-43606301, NEUTRAL0.3589120054297
PTPRF9670COSM6848138, pleuramesotheliomap.F1493LSubstitution - Missense1:43618737-43618737, NEUTRAL0.1830126928227
PTPRF9670COSM5025257, breastcarcinomap.V638ISubstitution - Missense1:43597846-43597846, NEUTRAL0.0860822722193