ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME032 EXOSC2 SNP Splice_site 9 133570980 G A 35 95 MEL MEL-13463 EXOSC2 SNP Missense_Mutation 9 133574767 G A 35 99 MEL MEL-JWCI-WGS-25 EXOSC2 SNP Silent 9 133573590 G T 47 76 OV TCGA-23-1117 EXOSC2 SNP Missense_Mutation 9 133578463 G T 35 85 CRC TCGA-AA-3679 EXOSC2 SNP Splice_site 9 133570879 G T 43 68 CRC TCGA-AA-3864 EXOSC2 SNP Missense_Mutation 9 133569236 C A 23 72 CRC TCGA-AG-A002 EXOSC2 SNP Missense_Mutation 9 133578479 C T 31 71 KIRC TCGA-B0-4693 EXOSC2 SNP Missense_Mutation 9 133578519 T A 55 90 UCEC TCGA-B5-A11E EXOSC2 SNP Nonsense_Mutation 9 133573555 C T 17 99 UCEC TCGA-BS-A0TC EXOSC2 SNP Missense_Mutation 9 133579087 G A 33 99 BLCA TCGA-DK-A1AC EXOSC2 SNP Missense_Mutation 9 133569207 C T 28 64