ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-12 BSND SNP Missense_Mutation 1 55472896 G A 43 51 MEL MEL-JWCI-WGS-13 BSND SNP Missense_Mutation 1 55472776 G A 41 62 MEL MEL-JWCI-WGS-24 BSND SNP Missense_Mutation 1 55473996 G A 41 56 MEL MEL-Ma-Mel-04 BSND SNP Missense_Mutation 1 55464947 C T 31 59 MEL MEL-Ma-Mel-28 BSND SNP Silent 1 55474199 A G 2 49 MEL MEL-Ma-Mel-48 BSND SNP Silent 1 55473902 C T 22 54 OV TCGA-04-1347 BSND SNP Silent 1 55472682 G A 34 63 LUAD TCGA-05-4382 BSND SNP Missense_Mutation 1 55464866 G T 45 84 LUAD TCGA-17-Z025 BSND SNP Missense_Mutation 1 55474144 G T 39 28 LUAD TCGA-17-Z031 BSND SNP Missense_Mutation 1 55472900 C T 29 56 LUSC TCGA-18-3417 BSND SNP Silent 1 55470715 C T 20 71 LUSC TCGA-18-3417 BSND SNP Missense_Mutation 1 55473948 G C 41 59 GBM TCGA-19-5960 BSND SNP Missense_Mutation 1 55470704 G A 40 52 LUSC TCGA-22-4607 BSND SNP Missense_Mutation 1 55464936 T A 51 82 LUAD TCGA-44-2657 BSND SNP Missense_Mutation 1 55474212 G A 33 79 LUAD TCGA-49-6767 BSND SNP Silent 1 55474247 C A 23 30 LUAD TCGA-50-6593 BSND SNP Silent 1 55472787 C T 24 51 LUSC TCGA-60-2720 BSND SNP Silent 1 55464892 C T 29 65 OV TCGA-61-2094 BSND SNP Missense_Mutation 1 55473915 C T 22 79 LUSC TCGA-66-2789 BSND SNP Missense_Mutation 1 55474046 C G 18 49 CRC TCGA-AA-3811 BSND SNP Missense_Mutation 1 55472757 A C 3 53 UCEC TCGA-B5-A0K9 BSND SNP Silent 1 55472943 C T 23 31 UCEC TCGA-B5-A11E BSND SNP Missense_Mutation 1 55464948 G A 39 62 UCEC TCGA-B5-A11E BSND SNP Silent 1 55470703 C T 31 46 BRCA TCGA-BH-A0C7 BSND SNP Missense_Mutation 1 55474123 C T 26 52 KIRC TCGA-BP-4967 BSND SNP Missense_Mutation 1 55464986 G A 40 45 KIRC TCGA-BP-5187 BSND SNP Missense_Mutation 1 55474113 T A 59 49 UCEC TCGA-D1-A15X BSND SNP Splice_Site 1 55472947 T C 59 58 UCEC TCGA-D1-A16X BSND SNP Silent 1 55472814 G A 37 43 BRCA TCGA-D8-A1JP BSND SNP Missense_Mutation 1 55464896 G T 48 52