ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B01246 CCND1 SNP Silent 11 69465912 G A 33 86 LUAD LUAD-RT-S01810 CCND1 SNP Silent 11 69462802 G T 39 25 LUAD LUAD_E00565 CCND1 SNP Missense_Mutation 11 69457826 G A 41 95 MEL ME024 CCND1 SNP Missense_Mutation 11 69466022 C T 22 87 MEL ME049 CCND1 SNP Missense_Mutation 11 69465970 G A 42 60 MM MM-0322 CCND1 SNP Missense_Mutation 11 69456092 A G 7 73 MM MM-0335 CCND1 SNP Missense 11 69456219 A T 4 59 MM MM-0427 CCND1 SNP Missense_Mutation 11 69456241 C G 26 92 MM MM-0429 CCND1 SNP Missense_Mutation 11 69456104 G A 46 92 MM MM-0429 CCND1 SNP Silent 11 69456210 C G 24 55 MM MM-0451 CCND1 SNP Missense_Mutation 11 69458005 G C 35 34 MM MM-0635 CCND1 SNP Missense_Mutation 11 69462891 G C 33 68 MM MM-442 CCND1 SNP Silent 11 69456108 A G 3 56 MM MM-442 CCND1 SNP Missense_Mutation 11 69456133 C T 22 78 MM MM-442 CCND1 SNP Silent 11 69456201 C T 24 61 LUAD TCGA-05-4426 CCND1 SNP Silent 11 69462817 C A 23 47 LUSC TCGA-34-2608 CCND1 SNP Missense_Mutation 11 69458669 G A 45 73 GBM TCGA-41-4097 CCND1 SNP Missense_Mutation 11 69457803 G T 46 95 LUAD TCGA-49-6742 CCND1 DNP Missense_Mutation 11 69458698 GG TA 39 32 LUAD TCGA-67-3771 CCND1 SNP Missense_Mutation 11 69456155 A C 10 73 UCEC TCGA-AP-A054 CCND1 SNP Missense_Mutation 11 69465889 T C 55 91 UCEC TCGA-AP-A0LM CCND1 SNP Missense_Mutation 11 69458005 G T 35 34 UCEC TCGA-AX-A05Z CCND1 SNP Missense_Mutation 11 69462881 T C 56 74 UCEC TCGA-AX-A062 CCND1 SNP Nonsense_Mutation 11 69465985 G T 41 64 UCEC TCGA-AX-A063 CCND1 SNP Missense_Mutation 11 69462905 G A 45 94 UCEC TCGA-AX-A0J0 CCND1 SNP Missense_Mutation 11 69458697 C T 27 54 UCEC TCGA-B5-A0JV CCND1 SNP Missense_Mutation 11 69466019 C T 17 100 HNSC TCGA-BA-4075 CCND1 SNP Silent 11 69462871 C T 26 94 UCEC TCGA-BG-A0M7 CCND1 SNP Missense_Mutation 11 69466019 C T 17 100 UCEC TCGA-BG-A0MQ CCND1 SNP Missense_Mutation 11 69465892 C A 24 62 UCEC TCGA-BG-A0VW CCND1 SNP Silent 11 69457918 C T 25 68 BRCA TCGA-BH-A0BP CCND1 SNP Missense_Mutation 11 69465940 C T 27 68 UCEC TCGA-BS-A0TJ CCND1 INS In_Frame_Ins 11 69466031 - GCG 59 92 UCEC TCGA-BS-A0U5 CCND1 SNP Missense_Mutation 11 69466040 T G 59 79 BLCA TCGA-BT-A20J CCND1 SNP Missense_Mutation 11 69456203 C T 31 92 HNSC TCGA-CN-4728 CCND1 SNP Silent 11 69457891 C T 26 68 HNSC TCGA-CV-6441 CCND1 SNP Missense_Mutation 11 69466006 G C 41 86 HNSC TCGA-CV-6441 CCND1 DEL In_Frame_Del 11 69466013 CTTGCACAC - 28 87 UCEC TCGA-D1-A0ZO CCND1 SNP Missense_Mutation 11 69466019 C T 17 100 UCEC TCGA-D1-A0ZU CCND1 SNP Missense_Mutation 11 69466021 C T 18 100 UCEC TCGA-D1-A163 CCND1 SNP Missense_Mutation 11 69466019 C T 17 100 UCEC TCGA-D1-A16D CCND1 DEL In_Frame_Del 11 69466027 GACGTGCGG - 37 100 UCEC TCGA-D1-A174 CCND1 SNP Missense_Mutation 11 69466022 C A 22 87 UCEC TCGA-D1-A17D CCND1 SNP Missense_Mutation 11 69466021 C T 18 100 BLCA TCGA-DK-A1AC CCND1 SNP Silent 11 69458749 C T 32 49