ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-038 KRT78 SNP Missense_Mutation 12 53241832 C T 26 54 LUAD LUAD-B01811 KRT78 SNP Silent 12 53240020 C T 29 75 LUAD LUAD-YINHD KRT78 SNP Missense_Mutation 12 53233070 G T 43 57 MEL ME014 KRT78 SNP Silent 12 53233763 G A 47 58 MEL MEL-JWCI-WGS-1 KRT78 SNP Silent 12 53240041 C T 21 53 MEL MEL-JWCI-WGS-1 KRT78 SNP Missense_Mutation 12 53241791 C T 30 52 MEL MEL-JWCI-WGS-12 KRT78 SNP Silent 12 53237949 C T 31 66 MEL MEL-JWCI-WGS-22 KRT78 SNP Missense_Mutation 12 53233093 C T 30 55 MEL MEL-JWCI-WGS-22 KRT78 SNP Silent 12 53240059 G A 41 66 MEL MEL-JWCI-WGS-25 KRT78 SNP Silent 12 53242361 G A 45 63 MEL MEL-JWCI-WGS-25 KRT78 SNP Missense_Mutation 12 53242615 C T 22 51 MEL MEL-Ma-Mel-48 KRT78 SNP Missense_Mutation 12 53233105 C T 22 36 MEL MEL-Ma-Mel-48 KRT78 SNP Silent 12 53237988 C T 24 71 MEL MEL-Ma-Mel-67 KRT78 SNP Silent 12 53241723 G A 35 52 OV TCGA-09-2050 KRT78 SNP Nonsense_Mutation 12 53238393 C A 30 63 LUSC TCGA-21-1070 KRT78 SNP Silent 12 53233571 C T 26 57 OV TCGA-23-2072 KRT78 SNP Missense_Mutation 12 53242380 G A 44 65 GBM TCGA-32-1977 KRT78 SNP Splice_site 12 53242331 C T 24 83 LUAD TCGA-49-4514 KRT78 DNP Missense_Mutation 12 53242431 GG TT 47 97 CRC TCGA-AA-3526 KRT78 SNP Missense_Mutation 12 53233617 G A 40 60 CRC TCGA-AA-3811 KRT78 SNP Silent 12 53238406 G A 38 0 CRC TCGA-AA-3864 KRT78 SNP Missense_Mutation 12 53240585 C T 19 49 CRC TCGA-AA-3971 KRT78 SNP Silent 12 53240569 G A 40 46 CRC TCGA-AA-A02J KRT78 SNP Missense_Mutation 12 53241719 G A 39 84 CRC TCGA-AG-A002 KRT78 SNP Nonsense_Mutation 12 53237996 C A 30 65 UCEC TCGA-AP-A056 KRT78 SNP Silent 12 53237961 C T 30 54 UCEC TCGA-AP-A059 KRT78 SNP Missense_Mutation 12 53241843 C A 24 57 UCEC TCGA-AX-A0J1 KRT78 SNP Missense_Mutation 12 53238425 C A 28 52 KIRC TCGA-B8-4151 KRT78 DEL In_Frame_Del 12 53242598 CCTGCTGCTGAAGCCGCC - 30 52 UCEC TCGA-BS-A0UF KRT78 SNP Missense_Mutation 12 53233608 T G 56 85 BLCA TCGA-C4-A0F6 KRT78 SNP Missense_Mutation 12 53241751 C A 31 66 BRCA TCGA-C8-A1HK KRT78 SNP Missense_Mutation 12 53233561 C T 22 65 HNSC TCGA-CN-4730 KRT78 SNP Missense_Mutation 12 53240016 C T 32 74 HNSC TCGA-CN-6997 KRT78 SNP Missense_Mutation 12 53237950 G A 40 56 HNSC TCGA-CQ-7068 KRT78 SNP Missense_Mutation 12 53238435 C G 30 75 HNSC TCGA-CR-7402 KRT78 SNP Missense_Mutation 12 53233651 G T 35 46 HNSC TCGA-CV-6956 KRT78 SNP Missense_Mutation 12 53241878 C T 18 60 KIRC TCGA-CZ-5989 KRT78 SNP Silent 12 53242514 C T 22 49 UCEC TCGA-D1-A103 KRT78 SNP Missense_Mutation 12 53233752 G A 42 59 UCEC TCGA-D1-A176 KRT78 SNP Missense_Mutation 12 53238401 C T 23 57 HNSC TCGA-D6-6515 KRT78 SNP Missense_Mutation 12 53233611 G A 40 50