ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-Ma-Mel-105 HSPBAP1 SNP Missense_Mutation 3 122459514 G A 39 47 LUAD TCGA-05-4396 HSPBAP1 SNP Missense_Mutation 3 122459244 G T 47 81 LUAD TCGA-05-4396 HSPBAP1 SNP Missense_Mutation 3 122459941 C A 23 68 GBM TCGA-06-0241 HSPBAP1 SNP Missense_Mutation 3 122459902 A G 7 74 OV TCGA-13-0913 HSPBAP1 SNP Silent 3 122487638 T A 51 48 GBM TCGA-14-0786 HSPBAP1 SNP Missense_Mutation 3 122459942 G A 39 80 LUSC TCGA-18-5592 HSPBAP1 SNP Nonsense_Mutation 3 122496727 C A 32 87 LUAD TCGA-44-2657 HSPBAP1 SNP Missense_Mutation 3 122459659 C A 29 52 LUAD TCGA-50-5049 HSPBAP1 SNP Missense_Mutation 3 122459941 C A 23 68 LUSC TCGA-66-2757 HSPBAP1 SNP Silent 3 122487665 G A 36 58 LUSC TCGA-66-2792 HSPBAP1 SNP Missense_Mutation 3 122512524 C G 26 71 UCEC TCGA-A5-A0GA HSPBAP1 SNP Missense_Mutation 3 122487561 G A 48 77 BRCA TCGA-A8-A07O HSPBAP1 SNP Missense_Mutation 3 122459670 G A 33 54 CRC TCGA-AA-A00N HSPBAP1 SNP Missense_Mutation 3 122487556 G T 33 47 KIRC TCGA-B0-4707 HSPBAP1 SNP Missense_Mutation 3 122459679 G T 46 61 UCEC TCGA-B5-A11E HSPBAP1 SNP Missense_Mutation 3 122459317 T C 50 40 UCEC TCGA-B5-A11E HSPBAP1 SNP Silent 3 122459660 A G 5 46 UCEC TCGA-B5-A11R HSPBAP1 SNP Missense_Mutation 3 122471443 C G 29 95 HNSC TCGA-BB-4227 HSPBAP1 SNP Silent 3 122474119 C G 29 66 UCEC TCGA-BS-A0UF HSPBAP1 SNP Nonsense_Mutation 3 122496715 C A 32 73 UCEC TCGA-BS-A0UJ HSPBAP1 SNP Missense_Mutation 3 122459289 T G 63 50 BLCA TCGA-BT-A20O HSPBAP1 SNP Missense_Mutation 3 122459659 C T 29 52 BLCA TCGA-DK-A2I4 HSPBAP1 SNP Silent 3 122459618 C T 29 45 BRCA TCGA-E2-A14X HSPBAP1 SNP Missense_Mutation 3 122459884 G A 47 79 UCEC TCGA-FI-A2EW HSPBAP1 SNP Silent 3 122478202 C T 29 56