ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62863 HEXB SNP Synonymous 5 74016299 A G 16 36 LUAD LUAD-RT-S01769 HEXB SNP Missense_Mutation 5 74016529 G A 45 60 MEL ME009 HEXB SNP Missense_Mutation 5 73992858 G A 35 95 MEL MEL-JWCI-WGS-12 HEXB SNP Silent 5 74016326 C T 18 63 MM MM-0191 HEXB SNP De_novo_Start_OutOfFrame 5 73985210 G T 35 42 OV TCGA-24-1469 HEXB SNP Missense_Mutation 5 74014631 G C 43 80 BRCA TCGA-A2-A0YJ HEXB SNP Missense_Mutation 5 73981270 T C 63 60 UCEC TCGA-A5-A0GW HEXB SNP Nonsense_Mutation 5 74009409 C T 31 58 CRC TCGA-AA-3516 HEXB SNP Silent 5 74009342 T G 56 55 CRC TCGA-AA-3947 HEXB SNP Missense_Mutation 5 74009374 G A 40 46 CRC TCGA-AG-A002 HEXB SNP Missense_Mutation 5 73981317 T G 53 46 CRC TCGA-AG-A016 HEXB SNP Missense_Mutation 5 74014148 G A 41 60 UCEC TCGA-AP-A056 HEXB SNP Splice_Site 5 73985152 G T 33 84 UCEC TCGA-AP-A056 HEXB SNP Missense_Mutation 5 74016271 A G 5 72 BRCA TCGA-AR-A24V HEXB SNP Missense_Mutation 5 74014695 C G 32 73 UCEC TCGA-AX-A060 HEXB SNP Silent 5 74012460 C T 25 40 UCEC TCGA-AX-A0J0 HEXB SNP Missense_Mutation 5 73992830 A G 5 74 UCEC TCGA-B5-A11E HEXB SNP Silent 5 74009438 G A 42 48 UCEC TCGA-BK-A0CB HEXB SNP Missense_Mutation 5 73985275 C T 22 85 UCEC TCGA-BS-A0UA HEXB SNP Silent 5 73981173 C T 28 55 UCEC TCGA-BS-A0UF HEXB SNP Missense_Mutation 5 74001048 C T 26 100 UCEC TCGA-D1-A17Q HEXB SNP Missense_Mutation 5 73989527 G A 37 73 BRCA TCGA-E9-A1N5 HEXB SNP Missense_Mutation 5 73985157 C T 29 48 BLCA TCGA-G2-A2EO HEXB SNP Missense_Mutation 5 73981280 G A 45 58 BLCA TCGA-H4-A2HQ HEXB SNP Missense_Mutation 5 74014165 G C 41 100 CARC Carc-BWH5 HEXB SNP Missense_Mutation 5 74001102 C T 32 100