ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0047 SRF SNP Silent 6 43146042 C T 23 37 BRCA BR-0052 SRF SNP Splice_site 6 43146620 G A 35 73 ESO ESO-141 SRF SNP Missense_Mutation 6 43146552 C T 22 69 LUAD LUAD-D01603 SRF SNP Missense_Mutation 6 43146857 G T 39 61 MEL ME009 SRF SNP Silent 6 43143611 C T 25 83 MEL ME033 SRF SNP Silent 6 43146186 C T 21 51 MM MM-0482 SRF SNP Missense_Mutation 6 43146035 C T 19 82 MM MM-0566 SRF SNP Splice_Site 6 43143706 G T 44 95 OV TCGA-13-1404 SRF SNP Missense_Mutation 6 43144302 G T 34 64 GBM TCGA-19-2619 SRF SNP Missense_Mutation 6 43141721 C T 18 96 LUSC TCGA-66-2744 SRF SNP Missense_Mutation 6 43146615 C A 21 98 LUSC TCGA-66-2785 SRF SNP Missense_Mutation 6 43143550 C G 30 95 UCEC TCGA-A5-A0G9 SRF SNP Missense_Mutation 6 43144340 C T 21 94 CRC TCGA-AA-3949 SRF SNP Missense_Mutation 6 43141726 C A 24 82 CRC TCGA-AA-3984 SRF SNP Missense_Mutation 6 43146043 G A 38 95 CRC TCGA-AA-A01R SRF SNP Missense_Mutation 6 43143699 A G 8 88 UCEC TCGA-B5-A11U SRF SNP Missense_Mutation 6 43144316 A G 7 79 UCEC TCGA-BG-A0VX SRF SNP Missense_Mutation 6 43141804 G T 33 96 BRCA TCGA-BH-A0BF SRF SNP Missense_Mutation 6 43141698 G C 33 58 KIRC TCGA-BP-4166 SRF SNP Missense_Mutation 6 43143556 C A 22 95 HNSC TCGA-CN-6011 SRF SNP Silent 6 43144380 C T 29 70 KIRC TCGA-CZ-5984 SRF SNP Silent 6 43146557 G A 35 64 UCEC TCGA-D1-A103 SRF SNP Silent 6 43141653 G A 48 61 UCEC TCGA-D1-A103 SRF SNP Missense_Mutation 6 43141687 A C 12 89 BRCA TCGA-D8-A1JJ SRF SNP Silent 6 43141677 G C 46 56