Gene Name HGNC ID COSMIC_MutID Primary sitePrimary histology AA-Mutation Mutation Type Genomic PositionFATHMM predictionFATHMM scoreLiterature evidence
PTPRN9676COSM1614394, livercarcinomap.E680KSubstitution - Missense2:219297283-219297283, PATHOGENIC0.97783Info_not_available
PTPRN9676COSM142782, skinmalignant_melanomap.Q143*Substitution - Nonsense2:219302788-219302788, PATHOGENIC0.9655919074898
PTPRN9676COSM142784, skinmalignant_melanomap.G262ESubstitution - Missense2:219302346-219302346, PATHOGENIC0.8881319074898
PTPRN9676COSM142783, skinmalignant_melanomap.E202KSubstitution - Missense2:219302611-219302611, PATHOGENIC0.8744919074898
PTPRN9676COSM142786, skinmalignant_melanomap.G731ESubstitution - Missense2:219297029-219297029, NEUTRAL0.1671519074898
PTPRN9676COSM142781, skinmalignant_melanomap.R122PSubstitution - Missense2:219303747-219303747, NEUTRAL0.0246919074898
PTPRN9676COSM142785, skinmalignant_melanomap.S429FSubstitution - Missense2:219300135-219300135, NEUTRAL0.0157419074898
PTPRN9676COSM308699, lungcarcinomap.T866fs*35Insertion - Frameshift2:219295053-219295054, Info_not_availableInfo_not_available22941188
PTPRN9676COSM142779, COSM142780, skinmalignant_melanomap.G65R, p.P121SSubstitution - Missense2:219303751-219303751, 2:219307531-219307531, Info_not_available0.56365, .5949919074898