ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD TCGA-17-Z045 COPS7B SNP Missense_Mutation 2 232663663 G T 44 82 LUSC TCGA-21-5782 COPS7B SNP Missense_Mutation 2 232660884 C G 29 68 LUSC TCGA-22-5473 COPS7B SNP Missense_Mutation 2 232653351 G C 42 93 OV TCGA-24-1563 COPS7B SNP Missense_Mutation 2 232660972 A G 8 65 LUAD TCGA-44-2668 COPS7B SNP Missense_Mutation 2 232672272 C T 19 86 GBM TCGA-76-6285 COPS7B SNP Missense_Mutation 2 232653347 A T 7 83 BRCA TCGA-A1-A0SP COPS7B SNP Missense_Mutation 2 232653392 C T 30 93 CRC TCGA-AA-A01R COPS7B SNP Missense_Mutation 2 232672230 G A 38 86 UCEC TCGA-AX-A0J1 COPS7B SNP Missense_Mutation 2 232659000 G A 34 88 HNSC TCGA-BA-7269 COPS7B SNP Missense_Mutation 2 232653363 C A 20 93