ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B02050 FAM26E SNP Silent 6 116836996 G T 40 40 LUAD LUAD-F00121 FAM26E SNP Missense_Mutation 6 116833358 G A 40 63 LUAD LUAD-S01413 FAM26E SNP Missense_Mutation 6 116833260 G T 36 57 MEL ME044 FAM26E SNP Missense_Mutation 6 116836892 G A 41 74 MEL MEL-JWCI-WGS-1 FAM26E SNP Missense_Mutation 6 116833274 G A 41 61 MEL MEL-JWCI-WGS-12 FAM26E SNP Missense_Mutation 6 116836973 C A 26 69 MEL MEL-JWCI-WGS-34 FAM26E SNP Missense_Mutation 6 116836979 C T 30 51 MEL MEL-Ma-Mel-85 FAM26E SNP Silent 6 116837116 G A 37 37 MM MM-0524 FAM26E SNP Missense_Mutation 6 116836781 A G 12 69 LUAD TCGA-64-5781 FAM26E SNP Missense_Mutation 6 116837003 G T 46 98 CRC TCGA-AA-3977 FAM26E SNP Missense_Mutation 6 116836833 G A 37 68 CRC TCGA-AA-A010 FAM26E SNP Silent 6 116833255 G A 37 40 UCEC TCGA-AP-A059 FAM26E SNP Missense_Mutation 6 116833152 A G 14 50 UCEC TCGA-AP-A0LM FAM26E SNP Silent 6 116833024 C A 32 41 UCEC TCGA-AX-A0J0 FAM26E SNP Missense_Mutation 6 116833089 T G 62 74 UCEC TCGA-B5-A11E FAM26E SNP Silent 6 116836777 C T 26 57 UCEC TCGA-BS-A0TC FAM26E SNP Silent 6 116837113 G A 33 66 UCEC TCGA-BS-A0UJ FAM26E SNP Missense_Mutation 6 116836906 T A 49 39 UCEC TCGA-D1-A17U FAM26E SNP Silent 6 116836819 T C 60 53