ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-13 PPME1 SNP Missense_Mutation 11 73962730 G T 35 75 MEL MEL-Ma-Mel-36 PPME1 SNP Missense_Mutation 11 73950233 G C 33 89 LUAD TCGA-05-4403 PPME1 SNP Missense_Mutation 11 73950294 A G 10 70 LUAD TCGA-05-4415 PPME1 SNP Missense_Mutation 11 73950231 T A 49 82 GBM TCGA-06-0126 PPME1 SNP Silent 11 73964552 T C 60 64 GBM TCGA-06-5859 PPME1 SNP Missense_Mutation 11 73914828 A T 8 76 LUAD TCGA-17-Z010 PPME1 SNP Missense_Mutation 11 73941432 G A 45 100 CRC TCGA-AA-A01R PPME1 SNP Splice_site 11 73915489 C T 19 97 CRC TCGA-AA-A01R PPME1 SNP Missense_Mutation 11 73957184 G A 39 94 UCEC TCGA-AP-A051 PPME1 SNP Silent 11 73957183 C T 19 51 UCEC TCGA-AP-A054 PPME1 SNP Splice_Site 11 73936303 T C 57 91 UCEC TCGA-AP-A059 PPME1 SNP Missense_Mutation 11 73957221 G A 48 95 UCEC TCGA-BG-A0M4 PPME1 SNP Silent 11 73936272 T C 55 50 BRCA TCGA-BH-A1F8 PPME1 SNP Missense_Mutation 11 73882561 G C 37 81 HNSC TCGA-CV-7255 PPME1 SNP Silent 11 73962725 G A 42 53 UCEC TCGA-D1-A16X PPME1 SNP Missense_Mutation 11 73933406 G A 37 98 BLCA TCGA-DK-A2I4 PPME1 SNP Missense_Mutation 11 73882471 C G 31 81