ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0025 TRIM68 SNP Missense_Mutation 11 4621613 G A 39 58 LUAD LUAD-CHTN-Z4716A TRIM68 SNP Missense_Mutation 11 4622035 T A 50 58 LUAD LUAD-TJW61 TRIM68 SNP Silent 11 4622004 C T 24 51 MEL MEL-JWCI-WGS-15 TRIM68 SNP Silent 11 4621821 C A 30 51 MEL MEL-Ma-Mel-122 TRIM68 SNP Missense_Mutation 11 4621574 G A 41 78 MEL MEL-Ma-Mel-35 TRIM68 SNP Silent 11 4621926 G A 37 46 LUSC TCGA-18-3412 TRIM68 SNP Missense_Mutation 11 4624558 C T 29 54 OV TCGA-24-1545 TRIM68 SNP Missense_Mutation 11 4622020 C T 19 52 LUAD TCGA-35-3621 TRIM68 SNP Silent 11 4623478 C T 29 72 LUSC TCGA-37-4133 TRIM68 SNP Missense_Mutation 11 4626667 A T 7 82 LUSC TCGA-66-2766 TRIM68 DEL Splice_Site_Del 11 4624567 CCCACTGCAAGAGACAAAA - 30 55 LUSC TCGA-66-2791 TRIM68 SNP Silent 11 4621770 C T 29 65 BRCA TCGA-A2-A0EQ TRIM68 SNP Silent 11 4626420 C T 29 43 CRC TCGA-A6-3807 TRIM68 SNP Missense_Mutation 11 4622349 G A 33 81 BRCA TCGA-A8-A09R TRIM68 SNP Missense_Mutation 11 4621685 C T 19 53 CRC TCGA-AA-3666 TRIM68 SNP Silent 11 4621926 G A 37 46 CRC TCGA-AA-3672 TRIM68 SNP Missense_Mutation 11 4626437 G A 38 46 CRC TCGA-AA-3811 TRIM68 SNP Silent 11 4621713 C T 23 39 CRC TCGA-AA-3947 TRIM68 SNP Missense_Mutation 11 4621818 C A 24 53 UCEC TCGA-AP-A059 TRIM68 SNP Missense_Mutation 11 4626532 T C 60 50 UCEC TCGA-AX-A0J1 TRIM68 SNP Missense_Mutation 11 4621715 G A 42 53 HNSC TCGA-BA-6869 TRIM68 SNP Missense_Mutation 11 4621844 C G 20 79 UCEC TCGA-BG-A18B TRIM68 SNP Silent 11 4621922 G A 35 71 UCEC TCGA-BS-A0UV TRIM68 SNP Silent 11 4621686 G A 37 57 BLCA TCGA-C4-A0EZ TRIM68 SNP Nonsense_Mutation 11 4626603 C T 22 90 BLCA TCGA-CF-A3MI TRIM68 SNP Silent 11 4621770 C G 29 65 HNSC TCGA-CN-6023 TRIM68 SNP Missense_Mutation 11 4626315 C G 20 45 HNSC TCGA-CR-7386 TRIM68 SNP Missense_Mutation 11 4622349 G C 33 81 HNSC TCGA-CR-7398 TRIM68 SNP Missense_Mutation 11 4621792 T C 49 65 UCEC TCGA-E6-A1LZ TRIM68 SNP Missense_Mutation 11 4626698 C T 32 72