ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0025 RGS12 SNP Silent 4 3432495 G A 38 43 BRCA BR-0034 RGS12 SNP Missense_Mutation 4 3432152 C G 30 82 HNSC HN_63080 RGS12 SNP Nonsense 4 3418788 C G 29 96 LUAD LUAD-B00416 RGS12 SNP Missense_Mutation 4 3415828 G A 40 54 LUAD LUAD-CHTN-MAD06-00668 RGS12 SNP Missense_Mutation 4 3318582 G T 42 73 LUAD LUAD-E00897 RGS12 SNP Missense_Mutation 4 3432601 G A 41 93 LUAD LUAD-E01317 RGS12 SNP Missense_Mutation 4 3318381 G C 33 94 LUAD LUAD-F00162 RGS12 SNP Missense_Mutation 4 3319272 G A 39 60 LUAD LUAD-NYU284 RGS12 SNP Missense_Mutation 4 3319301 G T 43 58 LUAD LUAD-NYU284 RGS12 SNP Splice_Site 4 3424631 G T 34 71 LUAD LUAD-RT-S01831 RGS12 SNP Missense_Mutation 4 3430390 A C 1 66 LUAD LUAD_E00565 RGS12 SNP Missense_Mutation 4 3319162 G A 36 92 MEL ME017 RGS12 SNP Splice_site 4 3427286 G A 35 68 MEL MEL-JWCI-WGS-13 RGS12 DNP Missense_Mutation 4 3319454 CC TT 30 46 MEL MEL-JWCI-WGS-25 RGS12 SNP Missense_Mutation 4 3319705 C T 30 76 MEL MEL-Ma-Mel-63 RGS12 SNP Silent 4 3319196 G A 33 44 MEL MEL-Ma-Mel-65 RGS12 SNP Missense_Mutation 4 3319438 C T 30 74 MM MM-0248 RGS12 SNP Missense_Mutation 4 3318592 T C 59 87 MM MM-0423 RGS12 SNP Silent 4 3441261 G A 42 56 LUAD TCGA-05-4396 RGS12 SNP Silent 4 3429821 C A 23 60 LUAD TCGA-05-4420 RGS12 SNP Missense_Mutation 4 3432320 G T 39 49 GBM TCGA-06-2558 RGS12 SNP Missense_Mutation 4 3427237 T G 55 88 GBM TCGA-06-2559 RGS12 SNP Missense_Mutation 4 3432638 C T 23 77 OV TCGA-13-0920 RGS12 SNP Missense_Mutation 4 3319414 C G 32 62 LUAD TCGA-17-Z011 RGS12 DEL Frame_Shift_Del 4 3424168 C - 30 51 LUAD TCGA-17-Z015 RGS12 INS Frame_Shift_Ins 4 3432649 - CC 6 48 LUSC TCGA-21-5786 RGS12 SNP Nonsense_Mutation 4 3318114 A T 9 65 LUSC TCGA-22-5482 RGS12 SNP Missense_Mutation 4 3432376 A C 7 58 OV TCGA-24-1428 RGS12 SNP Synonymous 4 3430410 T C 50 61 LUSC TCGA-39-5031 RGS12 SNP Nonsense_Mutation 4 3418748 C T 25 73 LUSC TCGA-43-3920 RGS12 SNP Nonsense_Mutation 4 3318706 C A 31 94 LUAD TCGA-49-4487 RGS12 SNP Silent 4 3429845 A T 7 28 LUAD TCGA-50-5944 RGS12 SNP Missense_Mutation 4 3344679 C T 27 58 LUSC TCGA-60-2723 RGS12 SNP Silent 4 3427268 G A 35 56 LUSC TCGA-66-2787 RGS12 SNP Missense_Mutation 4 3319286 G T 43 51 LUSC TCGA-66-2792 RGS12 SNP Missense_Mutation 4 3424106 G A 41 88 LUAD TCGA-67-3771 RGS12 SNP Splice_site 4 3424297 G T 35 96 LUSC TCGA-70-6722 RGS12 SNP Missense_Mutation 4 3422404 G A 33 89 LUAD TCGA-73-4666 RGS12 SNP Missense_Mutation 4 3427249 G T 39 96 GBM TCGA-76-6191 RGS12 SNP Missense_Mutation 4 3319669 C T 27 49 LUAD TCGA-91-6829 RGS12 SNP Silent 4 3441279 G C 39 47 BRCA TCGA-A2-A0SU RGS12 SNP Missense_Mutation 4 3318650 C A 28 45 BRCA TCGA-A2-A0YK RGS12 SNP Missense_Mutation 4 3344728 C T 29 74 CRC TCGA-A6-2672 RGS12 DEL Frame_Shift_Del 4 3429853 AG - 7 53 CRC TCGA-A6-2676 RGS12 SNP Missense_Mutation 4 3318383 G T 34 54 CRC TCGA-AA-3667 RGS12 SNP Silent 4 3318002 G A 38 42 CRC TCGA-AA-3672 RGS12 SNP Missense_Mutation 4 3430412 A G 7 80 CRC TCGA-AA-3864 RGS12 SNP Missense_Mutation 4 3318583 C T 27 64 CRC TCGA-AA-3984 RGS12 SNP Nonsense_Mutation 4 3416494 G T 33 94 CRC TCGA-AA-A00J RGS12 SNP Silent 4 3318056 G T 39 26 CRC TCGA-AA-A00N RGS12 SNP Nonsense_Mutation 4 3430378 G T 33 86 CRC TCGA-AA-A01R RGS12 SNP Missense_Mutation 4 3318586 T C 51 87 AML TCGA-AB-2863 RGS12 SNP Silent 4 3318815 G A 39 11 UCEC TCGA-AP-A056 RGS12 SNP Missense_Mutation 4 3418677 T G 64 88 UCEC TCGA-AP-A059 RGS12 SNP Silent 4 3416529 C A 24 57 UCEC TCGA-AP-A059 RGS12 SNP Missense_Mutation 4 3417745 G A 46 81 UCEC TCGA-AP-A059 RGS12 SNP Silent 4 3424132 G A 33 51 UCEC TCGA-AP-A059 RGS12 SNP Missense_Mutation 4 3424244 C T 27 77 UCEC TCGA-AP-A059 RGS12 SNP Missense_Mutation 4 3430417 A C 4 80 UCEC TCGA-AP-A059 RGS12 SNP Missense_Mutation 4 3432637 C T 26 92 UCEC TCGA-AP-A0LM RGS12 SNP Silent 4 3318062 C T 31 37 UCEC TCGA-AP-A0LM RGS12 SNP Missense_Mutation 4 3418743 C T 31 83 UCEC TCGA-AX-A05Z RGS12 SNP Missense_Mutation 4 3318204 G A 37 73 UCEC TCGA-AX-A1C8 RGS12 SNP Splice_site 4 3419268 G A 39 70 KIRC TCGA-B0-4837 RGS12 SNP Splice_Site 4 3432133 G T 33 96 KIRC TCGA-B0-5701 RGS12 SNP Missense_Mutation 4 3318132 G T 33 96 UCEC TCGA-B5-A11E RGS12 SNP Missense_Mutation 4 3422408 C T 31 89 UCEC TCGA-B5-A11H RGS12 SNP Missense_Mutation 4 3441311 C T 26 50 BRCA TCGA-B6-A0X5 RGS12 SNP Missense_Mutation 4 3318059 T G 52 45 HNSC TCGA-BA-4077 RGS12 SNP Missense_Mutation 4 3441262 C T 27 51 HNSC TCGA-BB-7862 RGS12 SNP Silent 4 3419261 C T 19 42 BLCA TCGA-BT-A3PH RGS12 SNP Missense_Mutation 4 3432571 G C 45 79 BLCA TCGA-C4-A0F7 RGS12 SNP Missense_Mutation 4 3425321 G A 40 82 BLCA TCGA-CF-A27C RGS12 SNP Silent 4 3416499 C T 29 56 HNSC TCGA-CN-6022 RGS12 SNP Silent 4 3432594 G A 45 43 HNSC TCGA-CV-7427 RGS12 SNP Missense_Mutation 4 3317944 C T 31 51 UCEC TCGA-D1-A103 RGS12 SNP Missense_Mutation 4 3344679 C T 27 58 UCEC TCGA-D1-A103 RGS12 SNP Silent 4 3419135 C T 23 48 UCEC TCGA-D1-A167 RGS12 SNP Silent 4 3415869 C T 27 49 UCEC TCGA-D1-A167 RGS12 SNP Missense_Mutation 4 3432230 G A 40 79 UCEC TCGA-DI-A0WH RGS12 SNP Missense_Mutation 4 3425300 G A 40 96 BLCA TCGA-DK-A1AC RGS12 SNP Silent 4 3344756 C T 29 54 BLCA TCGA-DK-A1AC RGS12 SNP Splice_site 4 3424704 C T 31 74 HNSC TCGA-DQ-7592 RGS12 SNP Silent 4 3424168 C T 30 51 BRCA TCGA-E2-A15R RGS12 SNP Silent 4 3441258 C G 23 47 BLCA TCGA-GD-A2C5 RGS12 SNP Missense_Mutation 4 3441290 C T 28 53 BLCA TCGA-GV-A3QI RGS12 SNP Silent 4 3424264 G A 39 40 HNSC TCGA-H7-7774 RGS12 SNP Silent 4 3318626 G A 37 32