ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62237 FAM46C SNP Synonymous 1 118165589 A G 14 10 MEL MEL-JWCI-WGS-7 FAM46C DNP Missense_Mutation 1 118166443 CC TT 18 100 MM MM-0216 FAM46C SNP Missense_Mutation 1 118166098 C G 32 97 MM MM-0363 FAM46C SNP Missense_Mutation 1 118165758 G C 33 96 MM MM-0390 FAM46C SNP Missense 1 118166034 G T 41 83 MM MM-0406 FAM46C DEL In_frame_Del 1 118166046 ATC - 4 88 MM MM-0408 FAM46C SNP Missense 1 118166431 T G 59 90 MM MM-0412 FAM46C DEL Frame_Shift_Del 1 118165627 TAAC - 49 89 MM MM-0421-FIX FAM46C SNP Synonymous 1 118165562 G T 42 52 MM MM-0472 FAM46C SNP Missense_Mutation 1 118165759 A G 10 88 MM MM-0506 FAM46C SNP Nonsense_Mutation 1 118165497 G T 33 60 MM MM-0507 FAM46C SNP Missense_Mutation 1 118165924 T A 60 88 MM MM-0529 FAM46C SNP Missense_Mutation 1 118166211 G T 35 100 MM MM-0546 FAM46C SNP Silent 1 118166315 C T 29 100 MM MM-0554 FAM46C SNP Missense_Mutation 1 118166239 T G 56 92 MM MM-0576 FAM46C SNP Missense_Mutation 1 118166038 C G 32 96 MM MM-0576 FAM46C SNP Silent 1 118166117 C T 23 14 MM MM-0594 FAM46C SNP Missense_Mutation 1 118166059 C A 32 96 MM MM-0600 FAM46C SNP Missense_Mutation 1 118166042 C G 30 57 MM MM-0638 FAM46C SNP Nonsense_Mutation 1 118166202 G T 33 96 LUAD TCGA-05-4396 FAM46C SNP Missense_Mutation 1 118165836 C A 24 74 LUAD TCGA-05-4396 FAM46C SNP Silent 1 118166117 C A 23 14 LUAD TCGA-05-4396 FAM46C SNP Missense_Mutation 1 118166139 G T 39 83 LUAD TCGA-05-4396 FAM46C SNP Missense_Mutation 1 118166214 G T 39 86 LUAD TCGA-05-4396 FAM46C SNP Missense_Mutation 1 118166248 G T 39 100 LUAD TCGA-05-4396 FAM46C SNP Missense_Mutation 1 118166326 C A 23 100 GBM TCGA-06-0214 FAM46C SNP Missense_Mutation 1 118166248 G A 39 100 GBM TCGA-06-0241 FAM46C SNP Missense_Mutation 1 118165644 G A 40 82 OV TCGA-13-1510 FAM46C SNP Missense_Mutation 1 118165807 A T 7 66 GBM TCGA-16-1045 FAM46C SNP Missense_Mutation 1 118166577 G A 40 86 LUAD TCGA-17-Z045 FAM46C SNP Silent 1 118166264 A T 7 27 LUSC TCGA-18-3419 FAM46C SNP Missense_Mutation 1 118166109 C A 21 83 LUAD TCGA-35-3621 FAM46C SNP Missense_Mutation 1 118166014 G C 40 96 BRCA TCGA-A8-A09G FAM46C SNP Missense_Mutation 1 118166421 C T 31 78 CRC TCGA-AA-3949 FAM46C SNP Missense_Mutation 1 118166184 G A 38 73 BRCA TCGA-AN-A0FJ FAM46C SNP Missense_Mutation 1 118166379 G A 38 56 UCEC TCGA-AX-A060 FAM46C SNP Missense_Mutation 1 118165591 C A 24 97 UCEC TCGA-B5-A0K2 FAM46C SNP Missense_Mutation 1 118165644 G A 40 82 KIRC TCGA-B8-5550 FAM46C SNP Silent 1 118166327 G T 39 29 HNSC TCGA-BB-4227 FAM46C SNP Silent 1 118165574 C A 30 52 UCEC TCGA-BG-A0LX FAM46C SNP Silent 1 118166654 G T 46 83 BRCA TCGA-BH-A0DZ FAM46C SNP Silent 1 118166486 C T 29 85 UCEC TCGA-BS-A0TE FAM46C SNP Missense_Mutation 1 118165695 G A 40 75 UCEC TCGA-BS-A0UF FAM46C SNP Missense_Mutation 1 118166276 A C 1 50 HNSC TCGA-CN-6020 FAM46C SNP Missense_Mutation 1 118166445 G T 40 100 HNSC TCGA-CR-5248 FAM46C SNP Missense_Mutation 1 118166279 C G 29 86 HNSC TCGA-CR-7364 FAM46C SNP Silent 1 118165682 C T 29 74 UCEC TCGA-D1-A103 FAM46C SNP Silent 1 118166015 T C 58 28 UCEC TCGA-D1-A16F FAM46C SNP Missense_Mutation 1 118166310 T C 60 92