ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls1583 PTGIS SNP Missense_Mutation 20 48127601 C A 25 98 DLBCL DLBCL-Ls3615 PTGIS SNP Missense_Mutation 20 48127617 C A 26 84 ESO ESO-0103 PTGIS SNP Missense_Mutation 20 48129793 C T 19 95 ESO ESO-913 PTGIS SNP Missense_Mutation 20 48164418 G T 41 71 LUAD LUAD-D01751 PTGIS SNP Missense_Mutation 20 48164477 C A 24 50 LUAD LUAD-E01278 PTGIS SNP Missense_Mutation 20 48127653 C A 21 98 LUAD LUAD-RT-S01777 PTGIS SNP Missense_Mutation 20 48156245 T A 58 69 LUAD LUAD-S01315 PTGIS SNP Missense_Mutation 20 48130857 C T 23 62 MEL MEL-13543 PTGIS SNP Missense_Mutation 20 48164546 C T 22 71 MEL MEL-JWCI-WGS-1 PTGIS SNP Missense_Mutation 20 48164397 C T 29 79 MEL MEL-JWCI-WGS-11 PTGIS SNP Splice_site 20 48130930 C T 30 41 MEL MEL-JWCI-WGS-6 PTGIS SNP Silent 20 48124541 G A 41 46 MEL MEL-JWCI-WGS-7 PTGIS SNP Missense_Mutation 20 48164472 C T 31 80 MEL MEL-Ma-Mel-102 PTGIS SNP Silent 20 48164524 G T 41 51 MEL MEL-Ma-Mel-105 PTGIS SNP Missense_Mutation 20 48129621 G A 47 95 MEL MEL-Ma-Mel-114 PTGIS SNP Silent 20 48156147 G A 44 56 MEL MEL-Ma-Mel-122 PTGIS SNP Missense_Mutation 20 48124535 C A 20 51 MEL MEL-Ma-Mel-85 PTGIS SNP Silent 20 48129773 C T 26 49 MM MM-0546 PTGIS SNP Missense_Mutation 20 48140603 C G 26 76 LUAD TCGA-05-4398 PTGIS DEL Frame_Shift_Del 20 48140741 G - 35 65 GBM TCGA-06-0119 PTGIS SNP Nonsense_Mutation 20 48129691 G A 38 64 GBM TCGA-12-1597 PTGIS SNP Missense_Mutation 20 48140704 C T 23 65 LUAD TCGA-17-Z022 PTGIS SNP Missense_Mutation 20 48127626 G A 42 98 LUAD TCGA-17-Z040 PTGIS SNP Nonsense_Mutation 20 48130814 G T 37 50 OV TCGA-23-1022 PTGIS SNP Missense_Mutation 20 48130869 C A 26 64 OV TCGA-23-1032 PTGIS SNP Splice_Site 20 48129799 C T 32 95 OV TCGA-24-2288 PTGIS SNP Missense_Mutation 20 48130883 T C 52 63 LUAD TCGA-35-5375 PTGIS SNP Missense_Mutation 20 48129765 G T 34 82 LUAD TCGA-38-4625 PTGIS DEL Frame_Shift_Del 20 48130834 C - 26 51 LUSC TCGA-39-5030 PTGIS SNP Silent 20 48164500 C T 23 39 BRCA TCGA-A7-A26J PTGIS SNP Missense_Mutation 20 48124536 T G 54 51 BRCA TCGA-A8-A08S PTGIS INS Frame_Shift_Ins 20 48160880 - TG 32 55 CRC TCGA-AA-3555 PTGIS SNP Silent 20 48166609 G T 33 42 CRC TCGA-AA-3864 PTGIS SNP Missense_Mutation 20 48156157 C T 27 66 CRC TCGA-AA-3973 PTGIS SNP Silent 20 48129710 G A 40 47 CRC TCGA-AA-A00J PTGIS SNP Missense_Mutation 20 48127680 A G 12 54 CRC TCGA-AA-A010 PTGIS SNP Nonsense_Mutation 20 48129637 C A 32 81 CRC TCGA-AA-A01X PTGIS SNP Missense_Mutation 20 48124486 C T 19 52 CRC TCGA-AG-3890 PTGIS SNP Missense_Mutation 20 48156158 G A 37 65 UCEC TCGA-AP-A051 PTGIS SNP Missense_Mutation 20 48156217 C T 27 49 UCEC TCGA-AP-A051 PTGIS SNP Silent 20 48164425 C T 25 56 UCEC TCGA-AP-A0LM PTGIS SNP Splice_Site 20 48156259 C A 32 88 BRCA TCGA-AR-A0U1 PTGIS SNP Missense_Mutation 20 48124493 T A 60 46 UCEC TCGA-AX-A05Z PTGIS SNP Missense_Mutation 20 48130929 T C 62 84 UCEC TCGA-B5-A0JV PTGIS SNP Missense_Mutation 20 48129747 C T 27 95 UCEC TCGA-B5-A0JY PTGIS SNP Missense_Mutation 20 48130909 G T 33 58 UCEC TCGA-B5-A0JY PTGIS SNP Missense_Mutation 20 48164505 C T 31 93 UCEC TCGA-B5-A0JY PTGIS SNP Missense_Mutation 20 48166656 C A 32 79 KIRC TCGA-B8-5552 PTGIS SNP Silent 20 48130813 C T 27 26 HNSC TCGA-BB-7870 PTGIS SNP Splice_site 20 48127716 C T 18 60 BLCA TCGA-BT-A0YX PTGIS SNP Silent 20 48130897 G C 33 47 HNSC TCGA-CR-7401 PTGIS SNP Missense_Mutation 20 48130868 G A 34 57 HNSC TCGA-CV-7432 PTGIS SNP Missense_Mutation 20 48124503 A G 8 85 BLCA TCGA-DK-A3IU PTGIS SNP Missense_Mutation 20 48124546 C G 30 56 BRCA TCGA-EW-A1J5 PTGIS SNP Silent 20 48164524 G A 41 51