ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0054 CCNB1 SNP Splice_site 5 68463108 A G 7 55 LUAD LUAD-F00162 CCNB1 SNP Missense_Mutation 5 68470210 G C 48 87 MM MM-0546 CCNB1 SNP Missense_Mutation 5 68470134 G A 45 100 LUSC TCGA-22-4613 CCNB1 SNP Silent 5 68470110 G C 47 53 LUSC TCGA-43-5668 CCNB1 SNP Missense_Mutation 5 68470119 A C 3 56 LUAD TCGA-50-5051 CCNB1 SNP Silent 5 68473356 C T 29 56 LUSC TCGA-60-2726 CCNB1 SNP Splice_Site 5 68473065 G C 33 86 LUAD TCGA-67-6217 CCNB1 SNP Missense_Mutation 5 68467140 C A 26 60 BRCA TCGA-A8-A092 CCNB1 DEL Splice_Site 5 68467280 GTAA - 44 99 CRC TCGA-AA-3966 CCNB1 SNP Missense_Mutation 5 68470115 G A 39 59 CRC TCGA-AA-A01K CCNB1 SNP Missense_Mutation 5 68467140 C T 26 60 UCEC TCGA-AP-A054 CCNB1 SNP Splice_site 5 68463091 T C 51 79 UCEC TCGA-AP-A056 CCNB1 SNP Missense_Mutation 5 68470860 A C 9 71 UCEC TCGA-AP-A059 CCNB1 SNP Silent 5 68471358 T C 59 53 UCEC TCGA-AX-A063 CCNB1 DEL Frame_Shift_Del 5 68464151 TT - 56 53 UCEC TCGA-AX-A0J1 CCNB1 SNP Missense_Mutation 5 68470918 G A 39 88 UCEC TCGA-B5-A0JY CCNB1 SNP Missense_Mutation 5 68470862 G T 33 60 UCEC TCGA-B5-A11E CCNB1 SNP Missense_Mutation 5 68464052 C A 24 81 UCEC TCGA-B5-A11E CCNB1 SNP Missense_Mutation 5 68470121 T C 58 92 UCEC TCGA-BS-A0UV CCNB1 SNP Missense_Mutation 5 68470114 C T 31 70 HNSC TCGA-CN-5356 CCNB1 SNP Silent 5 68473452 G A 35 51 HNSC TCGA-CV-7407 CCNB1 SNP Missense_Mutation 5 68467126 A C 1 56 HNSC TCGA-CX-7219 CCNB1 SNP Missense_Mutation 5 68471233 G A 37 87 BRCA TCGA-E2-A15K CCNB1 SNP Missense_Mutation 5 68470891 G T 44 79 HNSC TCGA-HL-7533 CCNB1 SNP Missense_Mutation 5 68470931 G C 33 58