ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0013 RNF214 SNP Missense_Mutation 11 117152044 C T 17 82 DLBCL DLBCL-Ls1620 RNF214 SNP Missense_Mutation 11 117109472 T G 60 53 HNSC HN_62421 RNF214 SNP Missense 11 117155807 C G 29 55 LUAD LUAD-NYU408 RNF214 SNP Missense_Mutation 11 117153233 G A 39 80 LUAD LUAD_E00522 RNF214 SNP Missense_Mutation 11 117105003 G T 35 62 MEL ME009 RNF214 SNP Silent 11 117109521 G A 44 52 MEL MEL-JWCI-27 RNF214 SNP Missense_Mutation 11 117110539 C T 29 54 MEL MEL-Ma-Mel-53 RNF214 SNP Missense_Mutation 11 117152058 C T 31 69 MEL Mel-BRAFi-03 RNF214 DNP Missense_Mutation 11 117153478 GG AA 39 81 LUAD TCGA-05-4396 RNF214 SNP Missense_Mutation 11 117109359 G T 45 51 LUAD TCGA-05-4396 RNF214 SNP Silent 11 117109606 C A 31 78 LUAD TCGA-05-4396 RNF214 SNP Nonsense_Mutation 11 117152352 G T 39 85 LUAD TCGA-05-4396 RNF214 SNP Missense_Mutation 11 117152676 G T 47 81 LUAD TCGA-17-Z022 RNF214 DNP Missense_Mutation 11 117109467 GG TT 35 54 LUAD TCGA-17-Z048 RNF214 SNP Missense_Mutation 11 117153155 C A 17 65 LUSC TCGA-37-3789 RNF214 SNP Missense_Mutation 11 117153509 C G 29 61 LUSC TCGA-66-2754 RNF214 SNP Silent 11 117150919 G T 47 56 UCEC TCGA-A5-A0GB RNF214 SNP Missense_Mutation 11 117152875 C T 22 79 CRC TCGA-AA-3715 RNF214 SNP Missense_Mutation 11 117152649 C A 32 65 CRC TCGA-AA-A010 RNF214 SNP Silent 11 117150669 C T 27 52 CRC TCGA-AG-3892 RNF214 SNP Missense_Mutation 11 117109610 C A 32 76 CRC TCGA-AG-3892 RNF214 SNP Missense_Mutation 11 117110570 G T 33 57 CRC TCGA-AG-A002 RNF214 SNP Nonsense_Mutation 11 117150911 G T 33 84 UCEC TCGA-AJ-A23M RNF214 SNP Missense_Mutation 11 117153160 C G 19 72 UCEC TCGA-AP-A051 RNF214 SNP Missense_Mutation 11 117153161 G A 40 84 UCEC TCGA-AP-A056 RNF214 SNP Missense_Mutation 11 117150675 A G 13 52 UCEC TCGA-AP-A056 RNF214 SNP Missense_Mutation 11 117152058 C T 31 69 UCEC TCGA-AP-A056 RNF214 SNP Missense_Mutation 11 117153160 C T 19 72 UCEC TCGA-AP-A059 RNF214 SNP Silent 11 117115292 G A 33 72 UCEC TCGA-AP-A05A RNF214 SNP Splice_site 11 117152119 G C 40 70 UCEC TCGA-AP-A0LM RNF214 SNP Missense_Mutation 11 117109649 G T 35 60 UCEC TCGA-B5-A0JY RNF214 SNP Missense_Mutation 11 117110559 G T 33 73 HNSC TCGA-BA-6869 RNF214 SNP Missense_Mutation 11 117153235 G A 44 53 BRCA TCGA-BH-A0DK RNF214 SNP Missense_Mutation 11 117152922 C A 21 71 UCEC TCGA-BS-A0UF RNF214 SNP Missense_Mutation 11 117109397 G T 33 77 UCEC TCGA-BS-A0UF RNF214 SNP Missense_Mutation 11 117110570 G T 33 57 UCEC TCGA-BS-A0UF RNF214 SNP Missense_Mutation 11 117152097 C T 31 70 UCEC TCGA-BS-A0UV RNF214 SNP Missense_Mutation 11 117152324 T G 61 52 UCEC TCGA-BS-A0UV RNF214 SNP Splice_site 11 117155869 G A 39 69 HNSC TCGA-CN-6011 RNF214 SNP Nonsense_Mutation 11 117110556 C T 29 72 HNSC TCGA-CN-6016 RNF214 SNP Missense_Mutation 11 117109781 A T 12 64 HNSC TCGA-CV-7411 RNF214 SNP Silent 11 117152363 G A 45 65 UCEC TCGA-D1-A103 RNF214 SNP Missense_Mutation 11 117117545 G T 35 54 UCEC TCGA-D1-A103 RNF214 SNP Splice_site 11 117155868 C T 19 47 BRCA TCGA-D8-A27H RNF214 SNP Missense_Mutation 11 117110556 C G 29 72 BRCA TCGA-E9-A295 RNF214 SNP Missense_Mutation 11 117109661 A C 9 62 BLCA TCGA-G2-A2EL RNF214 SNP Missense_Mutation 11 117105073 G A 37 73 CARC Carc-H55 RNF214 SNP Missense_Mutation 11 117109769 A G 12 52