ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CRC CRC-0009 FAM111B SNP Missense 11 58877139 C T 28 52 LUAD LUAD-B01811 FAM111B SNP Missense_Mutation 11 58893015 G T 44 49 LUAD LUAD-CHTN-MAD06-00668 FAM111B SNP Missense_Mutation 11 58892775 A C 16 70 LUAD LUAD-S01345 FAM111B SNP Missense_Mutation 11 58891936 G C 33 42 LUAD LUAD-S01345 FAM111B SNP Silent 11 58891951 G A 33 52 MEL MEL-Ma-Mel-65 FAM111B SNP Silent 11 58892305 T C 58 50 LUAD TCGA-05-4396 FAM111B SNP Missense_Mutation 11 58892585 C A 31 48 LUAD TCGA-05-4396 FAM111B SNP Silent 11 58892633 C A 23 51 LUAD TCGA-05-4396 FAM111B SNP Missense_Mutation 11 58892820 G T 39 40 OV TCGA-13-0885 FAM111B SNP Missense_Mutation 11 58892562 G A 34 52 LUSC TCGA-18-3406 FAM111B SNP Missense_Mutation 11 58893612 T C 52 75 LUSC TCGA-18-3411 FAM111B SNP Missense_Mutation 11 58893299 A G 4 65 OV TCGA-25-1313 FAM111B SNP Nonsense_Mutation 11 58893255 G A 47 45 LUSC TCGA-33-4566 FAM111B SNP Silent 11 58892264 C A 31 51 LUAD TCGA-38-4628 FAM111B SNP Missense_Mutation 11 58892054 C G 29 49 LUSC TCGA-39-5030 FAM111B SNP Missense_Mutation 11 58893237 C T 27 47 LUSC TCGA-46-3767 FAM111B SNP Silent 11 58892347 A G 16 51 LUAD TCGA-55-1592 FAM111B SNP Missense_Mutation 11 58891882 C A 27 48 UCEC TCGA-A5-A0VP FAM111B SNP Missense_Mutation 11 58893036 G A 37 42 CRC TCGA-AA-3555 FAM111B SNP Missense_Mutation 11 58893359 G A 37 38 CRC TCGA-AA-3977 FAM111B SNP Missense_Mutation 11 58892317 T G 64 61 CRC TCGA-AA-3984 FAM111B SNP Silent 11 58892779 G A 37 43 CRC TCGA-AA-A00K FAM111B SNP Nonsense_Mutation 11 58893362 C T 19 51 CRC TCGA-AA-A00N FAM111B SNP Silent 11 58892779 G A 37 43 CRC TCGA-AA-A00N FAM111B SNP Missense_Mutation 11 58893483 C T 19 42 CRC TCGA-AG-3601 FAM111B SNP Missense_Mutation 11 58877121 A G 9 58 CRC TCGA-AG-A002 FAM111B SNP Missense_Mutation 11 58891794 A C 2 49 CRC TCGA-AG-A002 FAM111B SNP Missense_Mutation 11 58892158 G T 33 49 CRC TCGA-AG-A002 FAM111B SNP Missense_Mutation 11 58892819 C T 31 42 CRC TCGA-AG-A002 FAM111B SNP Missense_Mutation 11 58893108 C T 27 49 CRC TCGA-AG-A002 FAM111B SNP Missense_Mutation 11 58893641 C A 32 52 BRCA TCGA-AN-A0XU FAM111B SNP Silent 11 58893517 C G 24 43 UCEC TCGA-AP-A051 FAM111B SNP Missense_Mutation 11 58892352 G A 41 57 UCEC TCGA-AP-A051 FAM111B SNP Silent 11 58892857 G A 34 47 UCEC TCGA-AP-A051 FAM111B SNP Silent 11 58893622 T A 60 44 UCEC TCGA-AP-A056 FAM111B SNP Missense_Mutation 11 58892748 C T 19 35 UCEC TCGA-AP-A059 FAM111B SNP Missense_Mutation 11 58892444 G A 45 61 UCEC TCGA-AP-A059 FAM111B SNP Nonsense_Mutation 11 58893085 G A 42 64 UCEC TCGA-AP-A059 FAM111B SNP Missense_Mutation 11 58893108 C T 27 49 UCEC TCGA-AX-A05Z FAM111B SNP Missense_Mutation 11 58891940 C A 29 53 UCEC TCGA-AX-A05Z FAM111B SNP Missense_Mutation 11 58893195 A C 4 17 UCEC TCGA-AX-A060 FAM111B SNP Missense_Mutation 11 58893105 G A 48 49 UCEC TCGA-AX-A063 FAM111B SNP Silent 11 58892671 G A 42 41 UCEC TCGA-AX-A0J0 FAM111B SNP Missense_Mutation 11 58892737 G T 33 50 UCEC TCGA-AX-A0J1 FAM111B SNP Missense_Mutation 11 58892924 G A 37 50 UCEC TCGA-B5-A0JY FAM111B SNP Missense_Mutation 11 58892543 C A 32 46 UCEC TCGA-B5-A11E FAM111B SNP Missense_Mutation 11 58892778 C T 23 60 UCEC TCGA-B5-A11J FAM111B SNP Missense_Mutation 11 58893237 C T 27 47 HNSC TCGA-BA-4075 FAM111B DEL Frame_Shift_Del 11 58892538 AAATT - 5 56 HNSC TCGA-BA-5149 FAM111B SNP Missense_Mutation 11 58892771 C G 29 60 BLCA TCGA-BL-A3JM FAM111B SNP Nonsense_Mutation 11 58893255 G A 47 45 UCEC TCGA-BS-A0UF FAM111B SNP Missense_Mutation 11 58893641 C A 32 52 BRCA TCGA-C8-A12P FAM111B DEL Frame_Shift_Del 11 58892505 GA - 41 48 KIRC TCGA-CJ-4635 FAM111B SNP Silent 11 58877131 A C 8 48 HNSC TCGA-CV-6948 FAM111B SNP Missense_Mutation 11 58892341 T A 51 42 HNSC TCGA-CV-7089 FAM111B SNP Silent 11 58891901 C T 24 57 UCEC TCGA-D1-A0ZO FAM111B SNP Silent 11 58892887 A G 9 45 UCEC TCGA-D1-A103 FAM111B SNP Missense_Mutation 11 58893158 T C 60 58 BLCA TCGA-DK-A3IN FAM111B SNP Missense_Mutation 11 58892744 C G 29 51 BLCA TCGA-DK-A3IN FAM111B SNP Nonsense_Mutation 11 58893519 C G 29 69 BLCA TCGA-GD-A3OP FAM111B SNP Missense_Mutation 11 58893123 C G 20 48