ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls2245 INO80D SNP Splice_site 2 206921666 A G 14 91 ESO ESO-1481 INO80D SNP Missense_Mutation 2 206869417 G A 40 99 HNSC HN_62602 INO80D SNP Missense 2 206927527 G A 37 100 LUAD LUAD-B01811 INO80D SNP Missense_Mutation 2 206921578 C A 24 97 LUAD LUAD-NYU284 INO80D SNP Silent 2 206892969 C T 21 97 LUAD LUAD-S01356 INO80D SNP Missense_Mutation 2 206921296 G C 35 66 LUAD LUAD-S01357 INO80D SNP Nonsense_Mutation 2 206874488 T A 61 77 LUAD LUAD-S01405 INO80D SNP Silent 2 206921388 C G 29 55 LUAD LUAD-S01405 INO80D SNP Missense_Mutation 2 206921621 C G 32 100 MEL MEL-JWCI-WGS-13 INO80D SNP Silent 2 206870039 G A 35 74 MM MM-0469 INO80D SNP Silent 2 206927633 A G 14 56 PRAD PR-01-1934 INO80D SNP Missense_Mutation 2 206869474 G C 33 99 LUAD TCGA-05-4396 INO80D SNP Missense_Mutation 2 206869637 G T 47 99 LUAD TCGA-05-4430 INO80D SNP Missense_Mutation 2 206869874 T A 59 56 LUSC TCGA-21-1076 INO80D SNP Silent 2 206911302 T A 55 53 LUSC TCGA-21-5787 INO80D SNP Missense_Mutation 2 206927738 C A 17 100 LUSC TCGA-22-4591 INO80D SNP Missense_Mutation 2 206869230 C A 28 73 OV TCGA-24-2298 INO80D SNP Missense_Mutation 2 206869178 T C 49 89 OV TCGA-24-2298 INO80D SNP Missense_Mutation 2 206927647 C T 23 100 LUSC TCGA-34-5240 INO80D SNP Silent 2 206869731 T C 52 81 LUSC TCGA-39-5039 INO80D SNP Missense_Mutation 2 206870222 C A 26 98 LUAD TCGA-50-5946 INO80D SNP Silent 2 206874387 G A 43 54 LUSC TCGA-60-2719 INO80D SNP Silent 2 206921016 G A 33 67 OV TCGA-61-2094 INO80D SNP Silent 2 206869554 G T 43 46 LUAD TCGA-73-4668 INO80D SNP Missense_Mutation 2 206921452 G T 44 68 CRC TCGA-AA-3710 INO80D SNP Missense_Mutation 2 206892935 G A 46 81 CRC TCGA-AA-3947 INO80D DEL Frame_Shift_Del 2 206921296 G - 35 66 CRC TCGA-AG-3892 INO80D SNP Silent 2 206869647 G T 45 59 UCEC TCGA-AP-A059 INO80D SNP Missense_Mutation 2 206869499 G A 33 99 UCEC TCGA-AP-A0LM INO80D SNP Silent 2 206870229 G A 39 45 UCEC TCGA-AP-A0LM INO80D SNP Missense_Mutation 2 206921026 G A 42 98 UCEC TCGA-AX-A05S INO80D DEL In_Frame_Del 2 206921231 AAG - 1 51 UCEC TCGA-AX-A05Z INO80D SNP Missense_Mutation 2 206870180 C T 31 83 UCEC TCGA-AX-A0J1 INO80D SNP Missense_Mutation 2 206921026 G A 42 98 KIRC TCGA-B0-4822 INO80D SNP Missense_Mutation 2 206892941 A T 8 89 UCEC TCGA-B5-A0JR INO80D SNP Missense_Mutation 2 206920963 G A 44 98 UCEC TCGA-B5-A11E INO80D SNP Missense_Mutation 2 206870221 G T 34 98 UCEC TCGA-B5-A11E INO80D SNP Missense_Mutation 2 206921224 G T 35 75 UCEC TCGA-B5-A11E INO80D SNP Splice_Site 2 206927770 C A 28 100 UCEC TCGA-B5-A11X INO80D SNP Missense_Mutation 2 206874391 C T 31 99 KIRC TCGA-BP-4158 INO80D SNP Missense_Mutation 2 206882406 T A 52 91 UCEC TCGA-BS-A0UV INO80D SNP Silent 2 206869530 G A 38 46 UCEC TCGA-BS-A0UV INO80D SNP Missense_Mutation 2 206920931 G A 41 76 BLCA TCGA-BT-A2LB INO80D SNP Silent 2 206921331 C T 32 64 BLCA TCGA-BT-A3PJ INO80D SNP Missense_Mutation 2 206869295 C T 29 82 KIRC TCGA-CJ-5678 INO80D SNP Missense_Mutation 2 206870035 C G 22 69 HNSC TCGA-CQ-5332 INO80D SNP Missense_Mutation 2 206869901 G A 43 74 HNSC TCGA-CV-7099 INO80D SNP Missense_Mutation 2 206869474 G C 33 99 HNSC TCGA-CV-7242 INO80D SNP Silent 2 206869167 A G 15 32 BLCA TCGA-DK-A1A5 INO80D SNP Missense_Mutation 2 206872011 C T 29 97 BLCA TCGA-DK-A1AB INO80D SNP Splice_site 2 206884568 T A 51 56 BLCA TCGA-DK-A2I4 INO80D SNP Missense_Mutation 2 206870253 C G 32 68 BRCA TCGA-E9-A1R7 INO80D SNP Missense_Mutation 2 206869432 G T 41 99 UCEC TCGA-EO-A1Y8 INO80D SNP Missense_Mutation 2 206882451 C A 29 100