ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62854 TRIM14 SNP Missense 9 100850183 C T 19 36 LUAD LUAD-5V8LT TRIM14 SNP Missense_Mutation 9 100881439 G A 35 63 LUAD LUAD-CHTN-MAD06-00678 TRIM14 SNP Splice_Site 9 100872169 G A 46 51 MEL MEL-JWCI-WGS-5 TRIM14 SNP Missense_Mutation 9 100854238 G A 44 66 MM MM-0546 TRIM14 SNP Silent 9 100881369 G A 33 53 LUAD TCGA-05-4396 TRIM14 SNP Silent 9 100857228 G T 39 48 LUSC TCGA-18-4086 TRIM14 SNP Missense_Mutation 9 100881413 A G 8 36 GBM TCGA-26-5136 TRIM14 SNP Missense_Mutation 9 100857227 C T 19 52 CRC TCGA-AA-3877 TRIM14 SNP Nonsense_Mutation 9 100854209 G A 38 54 AML TCGA-AB-2808 TRIM14 SNP Nonsense_Mutation 9 100849785 C T 22 70 UCEC TCGA-B5-A0JY TRIM14 SNP Missense_Mutation 9 100862360 C A 32 66 HNSC TCGA-BA-4077 TRIM14 SNP Silent 9 100862396 G C 45 56 BRCA TCGA-BH-A0HQ TRIM14 SNP Nonsense_Mutation 9 100862246 G A 45 47 HNSC TCGA-CN-6019 TRIM14 SNP Silent 9 100862405 G A 45 54 HNSC TCGA-CR-6481 TRIM14 SNP Missense_Mutation 9 100872212 C T 29 74 UCEC TCGA-D1-A17Q TRIM14 SNP Missense_Mutation 9 100854205 G A 37 65 HNSC TCGA-D6-6516 TRIM14 SNP Missense_Mutation 9 100857229 G A 43 67 BRCA TCGA-E2-A1AZ TRIM14 SNP Missense_Mutation 9 100862335 G A 34 61 CARC Carc-Asa16 TRIM14 SNP Missense_Mutation 9 100849795 A G 7 65