ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-173 KRTAP5-3 SNP Silent 11 1628995 T G 55 40 MEL MEL-JWCI-WGS-29 KRTAP5-3 SNP Silent 11 1629292 C T 24 53 MEL MEL-JWCI-WGS-34 KRTAP5-3 SNP Missense_Mutation 11 1629423 C T 22 57 OV TCGA-04-1356 KRTAP5-3 SNP Silent 11 1629565 A G 6 45 GBM TCGA-12-5295 KRTAP5-3 SNP Missense_Mutation 11 1629152 C G 25 89 LUAD TCGA-17-Z055 KRTAP5-3 SNP Missense_Mutation 11 1629042 G A 44 48 LUSC TCGA-22-5472 KRTAP5-3 SNP Missense_Mutation 11 1629521 C A 26 84 OV TCGA-24-1436 KRTAP5-3 SNP Missense_Mutation 11 1629081 C A 24 45 LUAD TCGA-44-3918 KRTAP5-3 SNP Missense_Mutation 11 1629527 C T 26 63 LUSC TCGA-66-2734 KRTAP5-3 SNP Missense_Mutation 11 1629296 G A 41 40 CRC TCGA-AA-3966 KRTAP5-3 DEL Frame_Shift_Del 11 1629527 C - 26 63 UCEC TCGA-AP-A051 KRTAP5-3 SNP Silent 11 1628992 G T 34 75 UCEC TCGA-AP-A059 KRTAP5-3 SNP Silent 11 1629154 G A 34 57 UCEC TCGA-AX-A0J0 KRTAP5-3 SNP Missense_Mutation 11 1628905 C A 32 61 UCEC TCGA-AX-A0J0 KRTAP5-3 SNP Missense_Mutation 11 1629428 G A 41 49 UCEC TCGA-B5-A11E KRTAP5-3 SNP Silent 11 1629151 G A 34 58 UCEC TCGA-BG-A0M4 KRTAP5-3 SNP Silent 11 1629028 C T 20 49 KIRC TCGA-CJ-4634 KRTAP5-3 DEL Frame_Shift_Del 11 1629359 C - 26 72 HNSC TCGA-CN-6011 KRTAP5-3 SNP Silent 11 1628959 G A 46 51 HNSC TCGA-CR-6471 KRTAP5-3 SNP Missense_Mutation 11 1629441 A G 11 55 HNSC TCGA-CR-6484 KRTAP5-3 SNP Nonsense_Mutation 11 1629200 G C 45 43 HNSC TCGA-CR-7398 KRTAP5-3 DNP Missense_Mutation 11 1629194 CA AG 17 55 UCEC TCGA-D1-A103 KRTAP5-3 SNP Missense_Mutation 11 1629487 C A 28 63 UCEC TCGA-D1-A16X KRTAP5-3 SNP Silent 11 1629094 G A 34 75