ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62646 VARS SNP Synonymous 6 31760274 G A 41 47 LUAD LUAD-B00731 VARS SNP Silent 6 31747221 G A 45 50 LUAD LUAD-B00731 VARS SNP Silent 6 31749372 C G 29 59 LUAD LUAD-B01970 VARS SNP Missense_Mutation 6 31749723 C T 29 93 LUAD LUAD-QY22Z VARS SNP Silent 6 31760556 G A 47 52 LUAD LUAD-RT-S01477 VARS SNP Splice_site 6 31748796 C G 24 68 LUAD LUAD-S01409 VARS SNP Missense_Mutation 6 31747443 C A 23 76 MEL ME030 VARS SNP Silent 6 31752211 G A 37 57 MEL MEL-JWCI-WGS-1 VARS SNP Silent 6 31749494 A G 3 73 MEL MEL-JWCI-WGS-12 VARS SNP Missense_Mutation 6 31752183 C T 18 56 MEL MEL-JWCI-WGS-20 VARS SNP Missense_Mutation 6 31749483 C A 21 45 MEL MEL-JWCI-WGS-24 VARS SNP Missense_Mutation 6 31749490 G A 41 93 MM MM-0318 VARS SNP Missense_Mutation 6 31749280 G A 40 91 MM MM-0489 VARS SNP Missense_Mutation 6 31749678 C T 30 93 NB NB-1599 VARS SNP Silent 6 31750333 G A 48 91 LUAD TCGA-05-4396 VARS SNP Missense_Mutation 6 31749647 G T 35 80 LUAD TCGA-05-4402 VARS SNP Missense_Mutation 6 31752254 C T 27 94 GBM TCGA-06-6700 VARS SNP Missense_Mutation 6 31746760 T C 54 77 OV TCGA-13-1498 VARS SNP Missense_Mutation 6 31746775 G A 39 83 GBM TCGA-14-1034 VARS SNP Splice_Site 6 31749730 C T 24 93 LUAD TCGA-17-Z031 VARS SNP Missense_Mutation 6 31759427 G C 47 92 LUSC TCGA-18-3409 VARS SNP Nonsense_Mutation 6 31753355 C T 21 92 LUSC TCGA-18-3409 VARS SNP Silent 6 31760835 G A 35 59 LUSC TCGA-18-3409 VARS SNP Missense_Mutation 6 31760836 G A 44 87 LUSC TCGA-33-4566 VARS SNP Silent 6 31749688 C A 23 41 LUSC TCGA-33-4566 VARS SNP Missense_Mutation 6 31760824 C A 22 87 LUSC TCGA-34-5232 VARS SNP Missense_Mutation 6 31749681 G A 39 76 LUSC TCGA-34-5928 VARS SNP Missense_Mutation 6 31752382 G C 33 93 LUAD TCGA-49-4488 VARS SNP Splice_Site 6 31749539 C A 32 93 LUAD TCGA-49-4506 VARS SNP Splice_Site 6 31751989 A G 6 80 LUAD TCGA-50-5936 VARS SNP Missense_Mutation 6 31746796 G A 37 61 LUAD TCGA-73-4666 VARS SNP Silent 6 31747922 G A 42 58 CRC TCGA-AA-3858 VARS INS Frame_Shift_Ins 6 31746949 - G 55 67 AML TCGA-AB-2861 VARS SNP Silent 6 31752211 G A 37 57 BRCA TCGA-AO-A0JD VARS SNP Splice_site 6 31759746 C A 17 61 UCEC TCGA-AP-A051 VARS SNP Silent 6 31748674 G A 38 43 UCEC TCGA-AP-A051 VARS SNP Missense_Mutation 6 31750923 C T 23 92 UCEC TCGA-AP-A051 VARS SNP Missense_Mutation 6 31752422 G A 39 63 UCEC TCGA-AP-A056 VARS SNP Missense_Mutation 6 31748521 C T 31 77 UCEC TCGA-AP-A0LO VARS SNP Silent 6 31750214 C T 31 49 UCEC TCGA-AP-A0LT VARS SNP Missense_Mutation 6 31753448 G A 44 92 UCEC TCGA-AX-A0J1 VARS SNP Missense_Mutation 6 31760291 G A 43 57 KIRC TCGA-BP-4161 VARS DEL Frame_Shift_Del 6 31752484 GA - 45 80 UCEC TCGA-BS-A0UV VARS SNP Missense_Mutation 6 31752080 C T 31 52 KIRC TCGA-CJ-5672 VARS SNP Missense_Mutation 6 31752061 G A 46 94 HNSC TCGA-CN-6011 VARS SNP Silent 6 31750118 G C 41 51 HNSC TCGA-CN-6011 VARS SNP Splice_site 6 31759748 T G 50 85 HNSC TCGA-CN-6013 VARS SNP Silent 6 31749637 G A 45 51 HNSC TCGA-CN-6995 VARS SNP Missense_Mutation 6 31752467 C A 26 93 HNSC TCGA-CV-5966 VARS SNP Missense_Mutation 6 31749380 C T 32 80 HNSC TCGA-CV-6952 VARS SNP Missense_Mutation 6 31752260 G A 48 64 HNSC TCGA-DQ-7594 VARS SNP Nonsense_Mutation 6 31759487 G A 39 74 BLCA TCGA-G2-A2EK VARS SNP Missense_Mutation 6 31760629 C T 27 88