ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-LS4616 GNPTAB SNP Missense_Mutation 12 102154918 G A 39 98 ESO ESO-0079 GNPTAB SNP Silent 12 102164241 C A 26 49 LUAD LUAD-F00170 GNPTAB SNP Missense_Mutation 12 102224401 T C 49 65 LUAD LUAD-RT-S01774 GNPTAB SNP Missense_Mutation 12 102158320 G A 46 51 LUAD LUAD-S00488 GNPTAB SNP Missense_Mutation 12 102158249 A T 4 54 MEL ME009 GNPTAB SNP Missense_Mutation 12 102158288 C T 22 45 MEL MEL-Ma-Mel-122 GNPTAB SNP Missense_Mutation 12 102153873 G A 41 98 LUAD TCGA-17-Z053 GNPTAB SNP Nonsense_Mutation 12 102153823 G C 36 55 LUSC TCGA-22-4593 GNPTAB SNP Silent 12 102155097 T C 51 45 LUSC TCGA-22-5489 GNPTAB SNP Splice_Site 12 102161813 A G 14 77 OV TCGA-24-1616 GNPTAB SNP Nonsense_Mutation 12 102153834 G A 45 98 OV TCGA-24-2298 GNPTAB SNP Missense 12 102155355 C T 32 99 LUSC TCGA-33-4547 GNPTAB SNP Nonsense_Mutation 12 102158641 G C 45 64 LUAD TCGA-35-5375 GNPTAB SNP Silent 12 102160038 A C 6 32 LUAD TCGA-44-4112 GNPTAB SNP Silent 12 102179940 G A 35 68 LUAD TCGA-50-5066 GNPTAB SNP Missense_Mutation 12 102164889 T A 60 63 LUSC TCGA-60-2698 GNPTAB SNP Missense_Mutation 12 102158651 C A 29 51 LUAD TCGA-64-1678 GNPTAB SNP Missense_Mutation 12 102183810 C T 19 99 BRCA TCGA-A1-A0SJ GNPTAB SNP Missense_Mutation 12 102161847 G A 45 85 BRCA TCGA-A2-A04W GNPTAB SNP Nonsense_Mutation 12 102158936 G A 37 77 UCEC TCGA-A5-A0GP GNPTAB SNP Missense_Mutation 12 102151060 C T 27 100 BRCA TCGA-A8-A06Z GNPTAB SNP Missense_Mutation 12 102179874 A G 9 50 BRCA TCGA-A8-A076 GNPTAB SNP Missense_Mutation 12 102159934 T C 50 89 BRCA TCGA-A8-A07B GNPTAB DEL Frame_Shift_Del 12 102164928 A - 5 90 CRC TCGA-AA-3672 GNPTAB SNP Nonsense_Mutation 12 102158339 G A 46 50 CRC TCGA-AA-3845 GNPTAB SNP Silent 12 102158709 C T 23 36 CRC TCGA-AA-3977 GNPTAB SNP Missense_Mutation 12 102155433 G T 33 67 CRC TCGA-AA-3977 GNPTAB SNP Missense_Mutation 12 102161923 G A 42 85 CRC TCGA-AA-A00N GNPTAB SNP Missense_Mutation 12 102155046 A C 1 59 CRC TCGA-AA-A010 GNPTAB SNP Missense_Mutation 12 102158747 C T 31 48 AML TCGA-AB-2813 GNPTAB SNP Silent 12 102179965 G A 36 95 CRC TCGA-AG-3894 GNPTAB SNP Missense_Mutation 12 102183810 C T 19 99 CRC TCGA-AG-A002 GNPTAB SNP Missense_Mutation 12 102159074 G T 45 74 BRCA TCGA-AN-A04D GNPTAB SNP Missense_Mutation 12 102159023 G C 41 86 BRCA TCGA-AN-A0XW GNPTAB SNP Missense_Mutation 12 102153831 C T 30 98 UCEC TCGA-AP-A056 GNPTAB SNP Nonsense_Mutation 12 102164827 C A 32 99 UCEC TCGA-AP-A056 GNPTAB SNP Missense_Mutation 12 102183810 C T 19 99 UCEC TCGA-AP-A056 GNPTAB SNP Missense_Mutation 12 102224395 A C 11 62 UCEC TCGA-AP-A059 GNPTAB SNP Missense_Mutation 12 102158799 C A 24 50 UCEC TCGA-AP-A059 GNPTAB SNP Missense_Mutation 12 102158940 T C 61 49 UCEC TCGA-AP-A059 GNPTAB SNP Splice_Site 12 102160073 C A 24 74 UCEC TCGA-AP-A0LM GNPTAB SNP Missense_Mutation 12 102140955 C T 31 62 UCEC TCGA-AP-A0LM GNPTAB SNP Missense_Mutation 12 102151044 C T 19 100 UCEC TCGA-AP-A0LM GNPTAB SNP Nonsense_Mutation 12 102164297 G A 38 54 UCEC TCGA-AX-A05Z GNPTAB SNP Missense_Mutation 12 102158702 G T 35 52 UCEC TCGA-AX-A0J0 GNPTAB SNP Missense_Mutation 12 102158935 C T 31 99 UCEC TCGA-AX-A0J0 GNPTAB SNP Splice_site 12 102224339 C T 32 77 UCEC TCGA-AX-A0J1 GNPTAB SNP Missense_Mutation 12 102147186 C T 31 85 UCEC TCGA-AX-A0J1 GNPTAB SNP Silent 12 102155100 C T 19 28 KIRC TCGA-B0-5695 GNPTAB SNP Missense_Mutation 12 102163955 A T 4 50 KIRC TCGA-B2-5641 GNPTAB DEL Frame_Shift_Del 12 102158580 T - 56 55 UCEC TCGA-B5-A0JY GNPTAB SNP Silent 12 102155013 A G 16 52 UCEC TCGA-B5-A0JY GNPTAB SNP Missense_Mutation 12 102174022 A C 1 52 UCEC TCGA-B5-A0K4 GNPTAB SNP Nonsense_Mutation 12 102164827 C A 32 99 UCEC TCGA-B5-A11E GNPTAB SNP Missense_Mutation 12 102147161 C A 28 60 UCEC TCGA-B5-A11J GNPTAB SNP Missense_Mutation 12 102183722 G A 46 82 UCEC TCGA-B5-A11N GNPTAB SNP Missense_Mutation 12 102147186 C T 31 85 UCEC TCGA-B5-A11N GNPTAB SNP Missense_Mutation 12 102161839 C T 31 99 HNSC TCGA-BA-4074 GNPTAB SNP Missense_Mutation 12 102151077 A G 8 91 KIRC TCGA-BP-4164 GNPTAB SNP Silent 12 102161789 C T 19 44 UCEC TCGA-BS-A0UF GNPTAB SNP Nonsense_Mutation 12 102158198 C A 32 59 UCEC TCGA-BS-A0UF GNPTAB SNP Nonsense_Mutation 12 102174052 C A 32 99 UCEC TCGA-BS-A0UJ GNPTAB SNP Missense_Mutation 12 102140979 A T 16 57 UCEC TCGA-BS-A0UJ GNPTAB SNP Splice_Site 12 102164365 T C 55 93 UCEC TCGA-BS-A0UV GNPTAB SNP Missense_Mutation 12 102158081 C T 19 51 UCEC TCGA-BS-A0UV GNPTAB SNP Nonsense_Mutation 12 102174052 C A 32 99 KIRC TCGA-CJ-4640 GNPTAB SNP Missense_Mutation 12 102151009 C T 29 100 HNSC TCGA-CN-5364 GNPTAB SNP Missense_Mutation 12 102158435 T C 52 51 HNSC TCGA-CQ-5331 GNPTAB SNP Nonsense_Mutation 12 102153834 G A 45 98 HNSC TCGA-CR-6471 GNPTAB SNP Missense_Mutation 12 102153816 G A 41 98 HNSC TCGA-CV-7235 GNPTAB SNP Missense_Mutation 12 102159938 C G 27 84 HNSC TCGA-CV-7253 GNPTAB SNP Missense_Mutation 12 102155370 G C 39 75 KIRC TCGA-CZ-4853 GNPTAB SNP Silent 12 102179968 T C 59 38 UCEC TCGA-D1-A0ZV GNPTAB SNP Silent 12 102158901 G A 41 52 UCEC TCGA-D1-A101 GNPTAB SNP Silent 12 102183790 A G 8 50 UCEC TCGA-D1-A103 GNPTAB SNP Missense_Mutation 12 102141004 G A 38 61 UCEC TCGA-D1-A160 GNPTAB SNP Missense_Mutation 12 102164260 A G 4 92 UCEC TCGA-D1-A167 GNPTAB SNP Missense_Mutation 12 102158602 A G 14 91 UCEC TCGA-D1-A16X GNPTAB SNP Missense_Mutation 12 102158935 C T 31 99 UCEC TCGA-D1-A17Q GNPTAB SNP Missense_Mutation 12 102147186 C T 31 85 UCEC TCGA-DI-A1NN GNPTAB SNP Missense_Mutation 12 102147163 C T 29 98 BLCA TCGA-DK-A3IK GNPTAB SNP Nonsense_Mutation 12 102158444 G A 45 54 BRCA TCGA-EW-A1IX GNPTAB SNP Missense_Mutation 12 102151069 C T 32 100