ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-1163 FAM200A SNP Missense_Mutation 7 99145058 C G 19 49 OV TCGA-04-1525 FAM200A SNP Missense_Mutation 7 99145624 G C 41 55 GBM TCGA-06-0155 FAM200A SNP Missense_Mutation 7 99144668 G A 41 60 GBM TCGA-06-0174 FAM200A SNP Silent 7 99145995 A C 11 50 OV TCGA-24-1474 FAM200A SNP Missense_Mutation 7 99145297 C T 31 51 CRC TCGA-AA-3555 FAM200A SNP Missense_Mutation 7 99145140 A T 9 60 CRC TCGA-AA-3811 FAM200A SNP Missense_Mutation 7 99145142 A G 2 60 UCEC TCGA-AP-A059 FAM200A SNP Missense_Mutation 7 99144854 G A 39 50 KIRC TCGA-B0-4710 FAM200A SNP Missense_Mutation 7 99144587 A C 9 59 KIRC TCGA-B0-4710 FAM200A SNP Missense_Mutation 7 99144589 C T 20 60 UCEC TCGA-B5-A0JY FAM200A SNP Silent 7 99144588 A G 2 51 UCEC TCGA-B5-A11N FAM200A SNP Missense_Mutation 7 99145297 C T 31 51 KIRC TCGA-B8-4154 FAM200A SNP Missense_Mutation 7 99145313 G A 45 63 KIRC TCGA-BP-4162 FAM200A SNP Missense_Mutation 7 99145777 A T 12 62 KIRC TCGA-BP-4762 FAM200A SNP Missense_Mutation 7 99145240 G T 46 63 KIRC TCGA-BP-4775 FAM200A SNP Missense_Mutation 7 99144481 A G 13 59 UCEC TCGA-BS-A0UF FAM200A SNP Silent 7 99145599 G A 37 31 UCEC TCGA-BS-A0UF FAM200A SNP Missense_Mutation 7 99145681 C T 19 51 UCEC TCGA-BS-A0UV FAM200A SNP Missense_Mutation 7 99144807 C A 32 49 UCEC TCGA-D1-A103 FAM200A SNP Missense_Mutation 7 99144400 A C 11 59