ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls1899 KRT16 SNP Missense_Mutation 17 39768492 C T 19 65 ESO ESO-0167 KRT16 SNP Missense_Mutation 17 39768472 G A 38 54 LUAD LUAD-B02594 KRT16 SNP Silent 17 39768812 G C 47 50 LUAD LUAD-RT-S01702 KRT16 SNP Missense_Mutation 17 39767470 G C 33 55 LUAD LUAD_E00522 KRT16 SNP Missense_Mutation 17 39767206 G T 42 65 MED MD-331 KRT16 SNP Missense_Mutation 17 39767352 C T 27 61 MEL MEL-JWCI-WGS-1 KRT16 SNP Silent 17 39768431 G A 47 62 MEL MEL-JWCI-WGS-42 KRT16 SNP Missense_Mutation 17 39767213 C T 32 76 MEL MEL-Ma-Mel-54a KRT16 SNP Missense_Mutation 17 39768486 C A 21 65 MEL MEL-Ma-Mel-79 KRT16 SNP Silent 17 39768416 C T 30 55 MEL MEL-Ma-Mel-94 KRT16 SNP Missense_Mutation 17 39766595 C T 26 73 MM MM-0546 KRT16 SNP Silent 17 39767157 G A 41 55 GBM TCGA-06-0140 KRT16 SNP Silent 17 39767345 G A 40 18 GBM TCGA-06-0749 KRT16 SNP Missense_Mutation 17 39767641 C T 24 47 LUAD TCGA-17-Z016 KRT16 DEL Frame_Shift_Del 17 39767729 C - 26 44 LUSC TCGA-22-5472 KRT16 SNP Silent 17 39768836 C A 21 49 GBM TCGA-32-4213 KRT16 SNP Missense_Mutation 17 39768925 G A 39 56 LUSC TCGA-34-5231 KRT16 SNP Silent 17 39767163 C A 23 15 LUSC TCGA-43-6771 KRT16 SNP Missense_Mutation 17 39767921 G A 42 86 LUSC TCGA-46-3765 KRT16 INS Frame_Shift_Ins 17 39768931 - G 7 64 LUAD TCGA-49-4506 KRT16 SNP Missense_Mutation 17 39768924 C A 27 51 LUAD TCGA-50-5942 KRT16 SNP Missense_Mutation 17 39767654 C G 32 59 LUSC TCGA-66-2759 KRT16 SNP Missense_Mutation 17 39767629 C G 30 98 LUSC TCGA-66-2766 KRT16 SNP Silent 17 39768815 G T 43 49 GBM TCGA-76-4934 KRT16 SNP Silent 17 39766792 C T 21 74 CRC TCGA-AA-3977 KRT16 SNP Missense_Mutation 17 39766257 G A 37 65 CRC TCGA-AA-3984 KRT16 SNP Missense_Mutation 17 39767948 G A 38 69 UCEC TCGA-AP-A059 KRT16 SNP Missense_Mutation 17 39767921 G T 42 86 UCEC TCGA-AP-A0LM KRT16 SNP Missense_Mutation 17 39767654 C A 32 59 UCEC TCGA-AX-A0J1 KRT16 SNP Missense_Mutation 17 39766800 C A 28 62 KIRC TCGA-B0-5108 KRT16 SNP Missense_Mutation 17 39768515 G C 40 51 UCEC TCGA-B5-A11E KRT16 SNP Missense_Mutation 17 39767403 C T 27 51 UCEC TCGA-BG-A0M4 KRT16 SNP Missense_Mutation 17 39768852 C T 27 62 UCEC TCGA-BG-A0MQ KRT16 SNP Missense_Mutation 17 39766787 T G 60 50 HNSC TCGA-CN-5355 KRT16 SNP Missense_Mutation 17 39767694 C A 23 59 UCEC TCGA-D1-A16X KRT16 SNP Missense_Mutation 17 39767449 C T 32 66 UCEC TCGA-D1-A174 KRT16 SNP Silent 17 39768884 G A 46 59 UCEC TCGA-D1-A17Q KRT16 SNP Missense_Mutation 17 39767176 C T 27 55 UCEC TCGA-D1-A17Q KRT16 SNP Missense_Mutation 17 39767952 T G 62 92 BLCA TCGA-FD-A3N5 KRT16 SNP Missense_Mutation 17 39766722 T C 55 52