ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CLL CW113 ABT1 SNP Missense_Mutation 6 26598695 G A 40 76 DLBCL DLBCL-Ls378 ABT1 SNP Missense_Mutation 6 26598544 C T 27 96 LUAD LUAD-B01811 ABT1 SNP Missense_Mutation 6 26598785 G T 38 62 LUAD LUAD-NYU776 ABT1 SNP Splice_site 6 26597211 A G 8 60 LUAD LUAD-RT-S01301 ABT1 SNP Missense_Mutation 6 26598298 G T 38 65 LUAD LUAD-RT-S01813 ABT1 SNP Missense_Mutation 6 26597394 G C 40 65 MM MM-0607 ABT1 SNP Missense_Mutation 6 26597436 T C 56 84 MM MM-0638 ABT1 SNP Missense_Mutation 6 26598595 G A 45 97 LUAD TCGA-05-4396 ABT1 SNP Nonsense_Mutation 6 26598526 G T 37 97 LUAD TCGA-05-4397 ABT1 SNP Missense_Mutation 6 26598745 C T 19 58 OV TCGA-25-1632 ABT1 SNP Silent 6 26598254 C G 21 54 LUAD TCGA-50-5930 ABT1 SNP Nonsense_Mutation 6 26597220 G T 33 75 LUAD TCGA-50-6590 ABT1 SNP Missense_Mutation 6 26598587 C G 26 96 CRC TCGA-AA-3867 ABT1 SNP Missense_Mutation 6 26598593 G A 40 69 CRC TCGA-AA-A00N ABT1 SNP Missense_Mutation 6 26598192 A C 1 55 CRC TCGA-AG-A002 ABT1 SNP Missense_Mutation 6 26598209 G T 35 55 BRCA TCGA-AN-A0XS ABT1 SNP Missense_Mutation 6 26598210 G T 41 74 UCEC TCGA-AP-A051 ABT1 SNP Missense_Mutation 6 26598693 G T 34 59 UCEC TCGA-AP-A0LG ABT1 SNP Silent 6 26598284 G A 38 42 UCEC TCGA-AP-A0LM ABT1 SNP Missense_Mutation 6 26598655 G A 41 69 UCEC TCGA-B5-A0JY ABT1 SNP Missense_Mutation 6 26598743 G A 41 58 UCEC TCGA-B5-A11E ABT1 SNP Missense_Mutation 6 26598290 G T 47 71 UCEC TCGA-B5-A11E ABT1 SNP Missense_Mutation 6 26598304 G A 38 73 UCEC TCGA-B5-A11E ABT1 SNP Missense_Mutation 6 26598749 A C 9 60 KIRC TCGA-CJ-5682 ABT1 SNP Missense_Mutation 6 26598223 G T 41 96 HNSC TCGA-CV-6935 ABT1 SNP Silent 6 26597372 G T 38 51 HNSC TCGA-CV-7245 ABT1 SNP Missense_Mutation 6 26598238 G A 40 81 UCEC TCGA-D1-A15X ABT1 SNP Missense_Mutation 6 26598524 G A 34 97