ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-CHTN-Z4716A TRIM39 SNP Missense_Mutation 6 30310001 C A 18 77 MEL ME009 TRIM39 SNP Silent 6 30309988 G A 41 54 MEL MEL-JWCI-WGS-11 TRIM39 SNP Missense_Mutation 6 30309578 C T 23 75 MEL MEL-JWCI-WGS-24 TRIM39 SNP Silent 6 30309844 C T 21 50 MEL MEL-JWCI-WGS-38 TRIM39 SNP Nonsense_Mutation 6 30303651 C T 23 57 MEL MEL-Ma-Mel-05 TRIM39 SNP Missense_Mutation 6 30303610 C T 29 60 MEL MEL-Ma-Mel-102 TRIM39 SNP Missense_Mutation 6 30309816 T A 64 68 MEL MEL-Ma-Mel-122 TRIM39 SNP Missense_Mutation 6 30309618 C T 24 64 MEL Mel_BRAFi_02_PRE TRIM39 SNP Silent 6 30309586 C T 30 50 PRAD P06-3939 TRIM39 SNP Missense_Mutation 6 30314235 C G 17 65 PRAD PR-09-3983 TRIM39 SNP Silent 6 30297148 G T 39 48 OV TCGA-04-1362 TRIM39 SNP Missense_Mutation 6 30309530 G C 36 59 LUAD TCGA-05-4415 TRIM39 SNP Missense_Mutation 6 30297471 G C 46 90 OV TCGA-13-0920 TRIM39 SNP Missense_Mutation 6 30309785 G A 47 73 OV TCGA-25-1316 TRIM39 SNP Missense_Mutation 6 30308086 A G 12 41 LUSC TCGA-33-4586 TRIM39 SNP Silent 6 30309598 A T 5 47 LUSC TCGA-34-2600 TRIM39 SNP Missense_Mutation 6 30297303 G A 37 52 LUAD TCGA-49-4490 TRIM39 SNP Silent 6 30309601 G A 42 63 LUAD TCGA-50-6593 TRIM39 SNP Missense_Mutation 6 30309955 G T 42 71 LUSC TCGA-66-2744 TRIM39 SNP Missense_Mutation 6 30310025 G C 33 77 LUSC TCGA-66-2791 TRIM39 SNP Missense_Mutation 6 30309968 C T 22 79 LUAD TCGA-75-5146 TRIM39 SNP Missense_Mutation 6 30303750 A C 13 75 BRCA TCGA-A1-A0SN TRIM39 SNP Missense_Mutation 6 30298612 C T 31 65 CRC TCGA-A6-2676 TRIM39 SNP Missense_Mutation 6 30297399 G A 39 58 CRC TCGA-AA-3877 TRIM39 SNP Missense_Mutation 6 30297398 C T 23 51 UCEC TCGA-AP-A056 TRIM39 SNP Silent 6 30308067 C T 31 46 KIRC TCGA-B0-5115 TRIM39 SNP Missense_Mutation 6 30308093 C T 21 50 HNSC TCGA-CN-4726 TRIM39 SNP Missense_Mutation 6 30309645 C T 18 65 HNSC TCGA-CN-5360 TRIM39 SNP Missense_Mutation 6 30309588 C T 24 84 HNSC TCGA-CR-7398 TRIM39 SNP Silent 6 30297214 C T 29 49 HNSC TCGA-CV-6935 TRIM39 SNP Missense_Mutation 6 30297275 G A 33 60 HNSC TCGA-CV-6961 TRIM39 SNP Missense_Mutation 6 30297129 C T 32 58