ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CLL_170 KRT5 SNP Missense_Mutation 12 52910467 C T 19 75 DLBCL DLBCL-Ls1395 KRT5 SNP Missense_Mutation 12 52911894 A C 7 93 DLBCL DLBCL-MAYO_DLBCL_234 KRT5 SNP Missense_Mutation 12 52908962 C T 23 65 ESO ESO-0950 KRT5 SNP Silent 12 52910615 C T 23 47 ESO ESO-191 KRT5 SNP Missense_Mutation 12 52910638 C T 27 57 ESO ESO-913 KRT5 SNP Missense_Mutation 12 52913756 C T 23 54 LUAD LUAD-E00918 KRT5 SNP Silent 12 52912798 C A 21 9 LUAD LUAD-NYU776 KRT5 SNP Missense_Mutation 12 52912940 C A 23 100 LUAD LUAD-RT-S01774 KRT5 SNP Splice_Site 12 52911948 C T 24 100 LUAD LUAD-RT-S01856 KRT5 SNP Missense_Mutation 12 52911737 C T 26 70 LUAD LUAD-S01315 KRT5 SNP Silent 12 52908774 G C 45 52 LUAD LUAD-S01409 KRT5 SNP Splice_Site 12 52909581 C G 17 69 MEL ME014 KRT5 SNP Missense_Mutation 12 52913722 C T 30 61 MEL MEL-JWCI-WGS-1 KRT5 SNP Silent 12 52913610 G A 37 50 MEL MEL-JWCI-WGS-13 KRT5 SNP Missense_Mutation 12 52914058 G A 41 65 MEL MEL-JWCI-WGS-39 KRT5 SNP Silent 12 52913874 C T 22 51 MEL MEL-JWCI-WGS-7 KRT5 SNP Missense_Mutation 12 52911460 C T 30 60 MEL MEL-UKRV-Mel-20 KRT5 SNP Silent 12 52908864 C A 26 65 MM MM-0618 KRT5 SNP Silent 12 52913688 G T 34 50 PRAD PR-1701 KRT5 SNP Splice_site 12 52911537 T C 54 94 LUAD TCGA-05-4250 KRT5 SNP Silent 12 52910540 C T 32 79 LUAD TCGA-05-4382 KRT5 SNP Silent 12 52911461 C A 21 80 LUAD TCGA-05-4390 KRT5 SNP Missense_Mutation 12 52908997 C A 30 51 LUAD TCGA-05-5425 KRT5 SNP Splice_site 12 52912730 T A 56 70 LUAD TCGA-17-Z022 KRT5 SNP Missense_Mutation 12 52908971 C A 23 46 LUAD TCGA-17-Z023 KRT5 SNP Missense_Mutation 12 52910570 G T 48 61 LUAD TCGA-17-Z028 KRT5 SNP Missense_Mutation 12 52910607 T A 54 79 LUAD TCGA-17-Z031 KRT5 SNP Silent 12 52913793 G T 34 67 LUAD TCGA-17-Z045 KRT5 SNP Missense_Mutation 12 52913845 C A 20 82 LUSC TCGA-18-3409 KRT5 SNP Silent 12 52913697 A G 6 48 LUAD TCGA-38-4631 KRT5 SNP Missense_Mutation 12 52913777 C T 23 65 LUSC TCGA-43-5668 KRT5 SNP Silent 12 52913994 G A 46 53 LUAD TCGA-44-2656 KRT5 SNP Silent 12 52910579 A G 8 46 LUSC TCGA-60-2715 KRT5 SNP Silent 12 52913973 G C 43 56 LUAD TCGA-64-5781 KRT5 SNP Missense_Mutation 12 52912811 A T 7 92 LUSC TCGA-66-2789 KRT5 SNP Missense_Mutation 12 52914004 G A 33 56 BRCA TCGA-A8-A0A7 KRT5 SNP Silent 12 52910585 G A 45 60 CRC TCGA-AA-3966 KRT5 SNP Missense_Mutation 12 52913759 C T 23 75 CRC TCGA-AA-3984 KRT5 SNP Missense_Mutation 12 52911507 T C 58 94 CRC TCGA-AA-A00N KRT5 SNP Silent 12 52913760 G A 37 33 CRC TCGA-AA-A010 KRT5 SNP Missense_Mutation 12 52911411 C T 27 68 AML TCGA-AB-2807 KRT5 SNP Silent 12 52910546 G T 43 52 CRC TCGA-AG-3892 KRT5 SNP Splice_site 12 52909583 G T 33 58 CRC TCGA-AG-A002 KRT5 SNP Missense_Mutation 12 52913636 G T 33 86 CRC TCGA-AG-A002 KRT5 SNP Silent 12 52913943 G A 37 29 UCEC TCGA-AP-A0L8 KRT5 SNP Missense_Mutation 12 52908779 T G 55 72 UCEC TCGA-AP-A0LM KRT5 SNP Missense_Mutation 12 52912941 G A 38 75 UCEC TCGA-AP-A0LM KRT5 SNP Silent 12 52913610 G A 37 50 UCEC TCGA-AP-A0LM KRT5 SNP Silent 12 52913757 G A 38 49 UCEC TCGA-AX-A06H KRT5 SNP Silent 12 52910510 C T 25 54 KIRC TCGA-B0-5709 KRT5 SNP Missense_Mutation 12 52910988 C T 23 55 UCEC TCGA-B5-A0JY KRT5 SNP Missense_Mutation 12 52911437 C A 24 51 UCEC TCGA-B5-A0JY KRT5 SNP Silent 12 52912843 G A 37 37 UCEC TCGA-BK-A0C9 KRT5 SNP Nonsense_Mutation 12 52911523 G A 46 72 UCEC TCGA-BS-A0TC KRT5 SNP Silent 12 52913943 G A 37 29 UCEC TCGA-BS-A0TJ KRT5 SNP Missense_Mutation 12 52911411 C T 27 68 UCEC TCGA-BS-A0UF KRT5 SNP Missense_Mutation 12 52914043 C T 26 63 UCEC TCGA-BS-A0UV KRT5 SNP Splice_site 12 52909583 G T 33 58 BRCA TCGA-C8-A135 KRT5 SNP Silent 12 52913583 G T 39 20 HNSC TCGA-CN-4731 KRT5 SNP Missense_Mutation 12 52910945 C G 32 66 HNSC TCGA-CN-5373 KRT5 INS Frame_Shift_Ins 12 52913851 - ATCAA 28 70 HNSC TCGA-CN-5373 KRT5 INS Frame_Shift_Ins 12 52913991 - GT 47 72 HNSC TCGA-CQ-5323 KRT5 INS Frame_Shift_Ins 12 52911893 - A 29 54 HNSC TCGA-CQ-7065 KRT5 INS Frame_Shift_Ins 12 52911705 - T 36 66 HNSC TCGA-CR-7394 KRT5 SNP Silent 12 52913991 G A 47 72 HNSC TCGA-CV-6940 KRT5 SNP Nonsense_Mutation 12 52912854 C A 30 87 HNSC TCGA-CV-6961 KRT5 SNP Missense_Mutation 12 52910942 C G 29 65 HNSC TCGA-CV-7432 KRT5 SNP Missense_Mutation 12 52909018 A T 10 75 UCEC TCGA-D1-A17M KRT5 SNP Silent 12 52910981 G A 38 0 UCEC TCGA-D1-A17Q KRT5 SNP Missense_Mutation 12 52908953 G T 33 42 HNSC TCGA-H7-7774 KRT5 INS Frame_Shift_Ins 12 52913978 - GG 19 73 CARC Carc-DFCI-188 KRT5 SNP Missense_Mutation 12 52911475 G A 39 78 CARC Carc-H55 KRT5 SNP Silent 12 52910624 G A 40 33