ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-31 PTPMT1 SNP Silent 11 47593121 C T 30 67 LUAD TCGA-05-4396 PTPMT1 SNP Missense_Mutation 11 47593155 G T 47 51 CRC TCGA-AA-3984 PTPMT1 SNP Missense_Mutation 11 47593175 G T 33 41 CRC TCGA-AA-A01R PTPMT1 SNP Missense_Mutation 11 47593081 T A 50 88 UCEC TCGA-AP-A051 PTPMT1 SNP Missense_Mutation 11 47593141 G T 39 48 UCEC TCGA-AP-A059 PTPMT1 SNP Silent 11 47593061 C T 31 60 UCEC TCGA-B5-A11E PTPMT1 SNP Missense_Mutation 11 47591333 A C 9 62 HNSC TCGA-BB-4227 PTPMT1 SNP Missense_Mutation 11 47587500 G C 37 82 KIRC TCGA-CJ-4638 PTPMT1 SNP Missense_Mutation 11 47593082 C A 30 61 HNSC TCGA-CN-4730 PTPMT1 SNP Missense_Mutation 11 47593175 G C 33 41 BLCA TCGA-DK-A2I6 PTPMT1 SNP Missense_Mutation 11 47587500 G A 37 82