ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls3200 GDF11 SNP Silent 12 56142521 A T 10 50 ESO ESO-167 GDF11 SNP Silent 12 56143396 C T 29 65 PRAD PR-P559 GDF11 SNP Splice_site 12 56143668 G T 44 59 LUAD TCGA-05-4396 GDF11 SNP Missense_Mutation 12 56143376 C A 23 94 OV TCGA-24-2288 GDF11 SNP Silent 12 56137370 G A 35 61 CRC TCGA-AA-3672 GDF11 SNP Missense_Mutation 12 56142573 C T 27 63 CRC TCGA-AA-3821 GDF11 SNP Missense_Mutation 12 56143562 C A 22 96 CRC TCGA-AA-A010 GDF11 SNP Missense_Mutation 12 56142696 G A 37 92 UCEC TCGA-AP-A059 GDF11 SNP Missense_Mutation 12 56143508 A G 14 88 UCEC TCGA-B5-A11H GDF11 SNP Missense_Mutation 12 56143386 G A 37 94 UCEC TCGA-BG-A0MG GDF11 SNP Splice_site 12 56142370 C T 27 81 UCEC TCGA-BS-A0UJ GDF11 SNP Missense_Mutation 12 56142546 A G 10 61 UCEC TCGA-BS-A0UV GDF11 SNP Missense_Mutation 12 56142696 G A 37 92 BLCA TCGA-C4-A0F6 GDF11 SNP Missense_Mutation 12 56142751 C T 23 93 KIRC TCGA-CJ-4904 GDF11 SNP Nonsense_Mutation 12 56142619 C G 29 69 HNSC TCGA-CV-5430 GDF11 SNP Silent 12 56143303 T C 62 60 BLCA TCGA-DK-A3IS GDF11 SNP Missense_Mutation 12 56137466 C G 19 57 BLCA TCGA-GV-A3QI GDF11 SNP Missense_Mutation 12 56143318 C G 17 55 HNSC TCGA-HL-7533 GDF11 SNP Missense_Mutation 12 56142406 G A 46 94