ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-1488 FAM111A SNP Missense_Mutation 11 58920327 G C 33 81 HNSC HN_62672 FAM111A SNP Missense 11 58920402 G A 41 48 LUAD LUAD-CHTN-Z4716A FAM111A SNP Missense_Mutation 11 58920849 A G 15 53 LUAD LUAD-YINHD FAM111A SNP Missense_Mutation 11 58919953 G T 33 46 MEL ME009 FAM111A SNP Missense_Mutation 11 58919500 C T 20 47 MEL ME011 FAM111A SNP Silent 11 58919285 C T 18 45 MEL MEL-Ma-Mel-65 FAM111A SNP Missense_Mutation 11 58920178 T C 57 53 MEL MEL-Ma-Mel-94 FAM111A SNP Silent 11 58916378 C T 20 50 MM MM-0624 FAM111A SNP Missense_Mutation 11 58919237 A C 2 37 PRAD P04-2599 FAM111A SNP Missense_Mutation 11 58919785 C T 28 66 LUAD TCGA-05-4396 FAM111A SNP Nonsense_Mutation 11 58919562 G T 47 84 OV TCGA-09-1661 FAM111A SNP Missense_Mutation 11 58920846 C G 31 33 LUAD TCGA-17-Z037 FAM111A SNP Missense_Mutation 11 58919346 G C 33 56 GBM TCGA-19-5954 FAM111A SNP Silent 11 58919918 A G 15 48 OV TCGA-24-1418 FAM111A SNP Missense_Mutation 11 58920334 G C 36 55 OV TCGA-24-1563 FAM111A SNP Missense_Mutation 11 58920238 C G 20 49 LUSC TCGA-34-5928 FAM111A SNP Missense_Mutation 11 58920951 G C 33 61 LUSC TCGA-60-2698 FAM111A SNP Silent 11 58920584 G A 33 42 LUSC TCGA-60-2711 FAM111A SNP Silent 11 58920509 A T 16 28 BRCA TCGA-A1-A0SH FAM111A SNP Missense_Mutation 11 58920660 G A 33 49 CRC TCGA-A6-2676 FAM111A SNP Missense_Mutation 11 58919659 G A 35 49 CRC TCGA-AA-3867 FAM111A SNP Silent 11 58920140 G A 40 53 CRC TCGA-AA-3966 FAM111A SNP Missense_Mutation 11 58920196 G A 40 41 CRC TCGA-AG-A002 FAM111A SNP Silent 11 58919840 C A 24 50 CRC TCGA-AG-A002 FAM111A SNP Silent 11 58920755 T C 63 43 BRCA TCGA-AN-A0AR FAM111A DEL In_Frame_Del 11 58919851 ATG - 4 46 BRCA TCGA-AN-A0FD FAM111A SNP Silent 11 58920329 G A 34 47 UCEC TCGA-AP-A051 FAM111A SNP Missense_Mutation 11 58919530 G T 42 68 UCEC TCGA-AP-A056 FAM111A SNP Missense_Mutation 11 58919799 A G 2 67 UCEC TCGA-AP-A0LM FAM111A SNP Missense_Mutation 11 58920195 C T 19 46 UCEC TCGA-AP-A0LM FAM111A SNP Missense_Mutation 11 58920330 C T 26 51 UCEC TCGA-AP-A0LM FAM111A SNP Missense_Mutation 11 58920834 C A 21 47 KIRC TCGA-B0-5694 FAM111A SNP Missense_Mutation 11 58920102 A G 1 50 UCEC TCGA-B5-A0JY FAM111A SNP Missense_Mutation 11 58919492 G T 33 43 UCEC TCGA-B5-A0K1 FAM111A SNP Silent 11 58916408 C T 31 40 UCEC TCGA-B5-A11E FAM111A SNP Silent 11 58919864 A G 2 47 UCEC TCGA-BS-A0UF FAM111A SNP Missense_Mutation 11 58919526 C T 27 28 UCEC TCGA-BS-A0UF FAM111A SNP Silent 11 58919582 C T 30 53 UCEC TCGA-BS-A0UJ FAM111A SNP Missense_Mutation 11 58919517 A G 4 55 UCEC TCGA-BS-A0UV FAM111A SNP Missense_Mutation 11 58919674 C T 31 50 HNSC TCGA-CN-6020 FAM111A SNP Missense_Mutation 11 58919457 A T 16 46 HNSC TCGA-CR-6472 FAM111A SNP Silent 11 58920182 G T 45 48 HNSC TCGA-CR-6484 FAM111A SNP Silent 11 58920371 G A 45 60 HNSC TCGA-CV-6941 FAM111A SNP Missense_Mutation 11 58920865 G C 42 73 HNSC TCGA-CV-6961 FAM111A SNP Missense_Mutation 11 58919875 A G 2 69 UCEC TCGA-D1-A15X FAM111A SNP Missense_Mutation 11 58920814 C T 28 71 UCEC TCGA-D1-A177 FAM111A SNP Missense_Mutation 11 58919767 G A 38 31 UCEC TCGA-D1-A17Q FAM111A SNP Silent 11 58920029 C T 31 51 BRCA TCGA-EW-A1PD FAM111A SNP Missense_Mutation 11 58920622 C G 25 45