ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-184 CCND2 SNP Nonsense_Mutation 12 4409107 G T 39 54 ESO ESO-720 CCND2 SNP Missense_Mutation 12 4383276 G A 37 90 HNSC HN_62505 CCND2 SNP Missense 12 4383237 G A 44 56 HNSC HN_62505 CCND2 SNP Synonymous 12 4387967 G C 47 67 LUAD LUAD-B01145 CCND2 SNP Missense_Mutation 12 4383271 G A 37 48 LUAD LUAD-B02515 CCND2 SNP Missense_Mutation 12 4387986 G T 45 96 LUAD LUAD-CHTN-MAD06-00668 CCND2 SNP Silent 12 4385368 C A 29 68 LUAD LUAD-CHTN-Z4716A CCND2 SNP Missense_Mutation 12 4385183 C A 17 83 MED MD-057 CCND2 SNP Missense_Mutation 12 4409146 C T 22 93 MEL MEL-JWCI-WGS-25 CCND2 SNP Nonsense_Mutation 12 4387961 G A 41 96 MEL MEL-Ma-Mel-120 CCND2 SNP Nonsense_Mutation 12 4409098 C T 21 71 LUAD TCGA-17-Z022 CCND2 SNP Missense_Mutation 12 4398020 C T 26 96 LUSC TCGA-22-1012 CCND2 SNP Missense_Mutation 12 4409107 G C 39 54 GBM TCGA-27-2518 CCND2 SNP Nonsense_Mutation 12 4409083 C T 25 79 LUSC TCGA-60-2698 CCND2 DEL Frame_Shift_Del 12 4385331 C - 18 98 LUSC TCGA-60-2710 CCND2 SNP Silent 12 4385368 C A 29 68 LUSC TCGA-66-2780 CCND2 SNP Silent 12 4383320 T C 62 48 LUSC TCGA-66-2780 CCND2 SNP Missense_Mutation 12 4383326 G T 36 57 GBM TCGA-76-4928 CCND2 SNP Missense_Mutation 12 4398029 C G 21 96 CRC TCGA-AA-3525 CCND2 SNP Nonstop_Mutation 12 4409173 T C 59 86 UCEC TCGA-AP-A051 CCND2 SNP Missense_Mutation 12 4385219 A C 9 89 UCEC TCGA-AP-A0LG CCND2 SNP Nonsense_Mutation 12 4409088 C G 18 58 UCEC TCGA-AP-A0LM CCND2 SNP Missense_Mutation 12 4385256 C T 23 66 UCEC TCGA-AP-A0LM CCND2 SNP Splice_Site 12 4385387 G T 44 97 UCEC TCGA-AP-A0LM CCND2 SNP Missense_Mutation 12 4398043 G A 38 96 UCEC TCGA-AP-A0LM CCND2 SNP Missense_Mutation 12 4409158 C T 27 67 UCEC TCGA-AX-A0J1 CCND2 SNP Missense_Mutation 12 4383358 T G 50 81 KIRC TCGA-B8-5551 CCND2 SNP Silent 12 4398012 T C 61 50 UCEC TCGA-BS-A0UF CCND2 SNP Missense_Mutation 12 4398020 C T 26 96 UCEC TCGA-BS-A0UV CCND2 SNP Silent 12 4398036 G A 37 44 HNSC TCGA-CR-7373 CCND2 SNP Silent 12 4409145 C T 22 56 KIRC TCGA-CZ-5465 CCND2 SNP Missense_Mutation 12 4385304 C G 30 98 UCEC TCGA-D1-A17Q CCND2 SNP Splice_Site 12 4398007 G T 33 96