ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0051 VCL SNP Splice_site 10 75830841 G T 35 97 LUAD LUAD-B02050 VCL SNP Nonsense_Mutation 10 75830490 C G 29 98 LUAD LUAD-NYU259 VCL SNP Splice_Site 10 75802840 G A 35 82 LUAD LUAD_E00565 VCL SNP Missense_Mutation 10 75802868 G A 45 82 LUAD TCGA-05-4396 VCL SNP Silent 10 75855496 C A 31 47 LUAD TCGA-05-4398 VCL SNP Missense_Mutation 10 75842254 A G 5 89 LUSC TCGA-22-4595 VCL SNP Missense_Mutation 10 75854156 G C 45 97 LUSC TCGA-22-5472 VCL SNP Missense_Mutation 10 75855548 G T 46 82 OV TCGA-24-1556 VCL SNP Missense_Mutation 10 75857067 C T 30 68 GBM TCGA-32-1977 VCL SNP Silent 10 75849002 T C 54 48 LUAD TCGA-50-6593 VCL SNP Missense_Mutation 10 75874084 G T 39 71 OV TCGA-61-1998 VCL SNP Missense_Mutation 10 75857087 A T 3 58 BRCA TCGA-A8-A09M VCL SNP Silent 10 75860849 A C 6 40 CRC TCGA-AA-3554 VCL SNP Missense_Mutation 10 75860761 C T 19 96 CRC TCGA-AA-A00R VCL SNP Silent 10 75854134 G A 39 45 CRC TCGA-AG-A002 VCL SNP Missense_Mutation 10 75877872 G A 37 97 UCEC TCGA-AP-A051 VCL SNP Silent 10 75868839 C T 23 31 UCEC TCGA-AP-A054 VCL SNP Silent 10 75867085 G A 38 49 UCEC TCGA-AP-A056 VCL SNP Missense_Mutation 10 75867018 A G 16 76 UCEC TCGA-AP-A059 VCL SNP Missense_Mutation 10 75854158 G T 35 48 UCEC TCGA-AP-A0LM VCL SNP Missense_Mutation 10 75871687 G T 35 75 BRCA TCGA-AR-A1AY VCL SNP Nonsense_Mutation 10 75854054 C T 31 80 BRCA TCGA-AR-A24K VCL SNP Missense_Mutation 10 75834570 A G 4 90 UCEC TCGA-AX-A0J0 VCL SNP Missense_Mutation 10 75868840 G A 39 98 UCEC TCGA-AX-A0J1 VCL SNP Missense_Mutation 10 75834528 A G 2 70 UCEC TCGA-B5-A0JY VCL SNP Missense_Mutation 10 75849004 A G 7 90 UCEC TCGA-B5-A11E VCL SNP Splice_Site 10 75864808 G T 35 85 UCEC TCGA-B5-A11E VCL SNP Missense_Mutation 10 75873970 G A 38 99 UCEC TCGA-B5-A11Y VCL SNP Missense_Mutation 10 75874625 C T 23 67 BRCA TCGA-BH-A0HQ VCL SNP Missense_Mutation 10 75843202 G T 38 97 UCEC TCGA-BK-A0CC VCL SNP Silent 10 75874037 C T 29 55 KIRC TCGA-BP-4766 VCL SNP Missense_Mutation 10 75854046 C A 21 83 KIRC TCGA-BP-4981 VCL SNP Missense_Mutation 10 75860838 C G 23 79 UCEC TCGA-BS-A0U7 VCL SNP Missense_Mutation 10 75871772 C T 18 100 UCEC TCGA-BS-A0UJ VCL SNP Silent 10 75843245 T C 55 50 UCEC TCGA-BS-A0UV VCL SNP Missense_Mutation 10 75849096 G A 37 98 UCEC TCGA-BS-A0UV VCL SNP Missense_Mutation 10 75849811 G A 41 98 HNSC TCGA-CN-5374 VCL SNP Missense_Mutation 10 75874638 G C 36 99 HNSC TCGA-CQ-5326 VCL SNP Silent 10 75855484 G A 42 51 HNSC TCGA-CQ-5334 VCL SNP Missense_Mutation 10 75856965 C A 32 84 HNSC TCGA-CQ-5334 VCL SNP Missense_Mutation 10 75857067 C T 30 68 HNSC TCGA-CV-7427 VCL SNP Missense_Mutation 10 75877857 C T 28 97 HNSC TCGA-CX-7085 VCL SNP Missense_Mutation 10 75855416 C G 29 97 UCEC TCGA-D1-A17Q VCL SNP Missense_Mutation 10 75855510 G A 37 67 BRCA TCGA-E2-A10C VCL SNP Nonsense_Mutation 10 75832608 C A 29 99 BLCA TCGA-GV-A3JX VCL SNP Nonsense_Mutation 10 75849105 C T 29 98 HNSC TCGA-HL-7533 VCL SNP Missense_Mutation 10 75868828 G A 45 98