ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62832 PTPRCAP SNP Missense 11 67203434 C T 31 49 LUAD LUAD-F00368 PTPRCAP SNP Missense_Mutation 11 67203361 G A 40 32 MM MM-0492 PTPRCAP SNP Missense_Mutation 11 67203227 C T 22 62 LUSC TCGA-33-4538 PTPRCAP SNP Missense_Mutation 11 67203563 C T 24 57 LUAD TCGA-50-5931 PTPRCAP SNP Missense_Mutation 11 67203241 G T 46 66 LUSC TCGA-56-6546 PTPRCAP SNP Missense_Mutation 11 67203589 C A 23 55 KIRC TCGA-AK-3458 PTPRCAP SNP Missense_Mutation 11 67203476 G T 47 43 UCEC TCGA-AP-A059 PTPRCAP SNP Missense_Mutation 11 67203501 C A 24 52 UCEC TCGA-AX-A06H PTPRCAP SNP Missense_Mutation 11 67203361 G A 40 32 UCEC TCGA-B5-A0JY PTPRCAP SNP Missense_Mutation 11 67203434 C T 31 49 UCEC TCGA-D1-A17M PTPRCAP SNP Missense_Mutation 11 67203541 G A 34 49