ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL ME009 UQCRC1 SNP Silent 3 48642136 G A 43 50 MEL MEL-13447 UQCRC1 SNP Nonsense_Mutation 3 48642183 C A 30 100 MEL MEL-13561 UQCRC1 SNP Splice_site 3 48641668 G A 45 87 MEL MEL-JWCI-WGS-8 UQCRC1 SNP Missense_Mutation 3 48638807 G A 47 62 MEL MEL-Ma-Mel-36 UQCRC1 SNP Missense_Mutation 3 48643224 A T 1 52 PRAD PR-02-1736 UQCRC1 SNP Missense_Mutation 3 48637966 C A 18 100 OV TCGA-04-1530 UQCRC1 SNP Silent 3 48638211 G C 35 54 OV TCGA-09-2044 UQCRC1 DNP Missense_Mutation 3 48643278 CC AA 30 99 GBM TCGA-26-5134 UQCRC1 SNP Missense_Mutation 3 48641675 T C 54 56 LUAD TCGA-50-5049 UQCRC1 SNP Silent 3 48637934 G A 43 56 LUAD TCGA-50-6593 UQCRC1 SNP Silent 3 48646610 A G 11 48 BRCA TCGA-A1-A0SO UQCRC1 DEL In_Frame_Del 3 48638832 CTGCATATGTCCATGGGATGC - 32 70 BRCA TCGA-A8-A07O UQCRC1 SNP Missense_Mutation 3 48641015 C G 18 100 CRC TCGA-AA-3821 UQCRC1 SNP Missense_Mutation 3 48636569 G A 38 65 CRC TCGA-AA-A01S UQCRC1 SNP Missense_Mutation 3 48643256 C T 29 99 UCEC TCGA-AP-A056 UQCRC1 SNP Silent 3 48638130 G A 37 56 UCEC TCGA-AP-A056 UQCRC1 SNP Missense_Mutation 3 48641675 T G 54 56 UCEC TCGA-AP-A0LM UQCRC1 SNP Silent 3 48641052 G A 39 28 BLCA TCGA-BT-A0YX UQCRC1 SNP Silent 3 48641043 G A 45 49 HNSC TCGA-CR-7404 UQCRC1 SNP Missense_Mutation 3 48641703 G C 33 73 UCEC TCGA-D1-A163 UQCRC1 SNP Missense_Mutation 3 48636590 G A 39 81 BRCA TCGA-D8-A1JK UQCRC1 SNP Missense_Mutation 3 48637563 T C 58 77