ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-D02185 PRAMEF18 SNP Missense_Mutation 1 13695853 G T 35 58 LUAD LUAD_E00522 PRAMEF18 SNP Missense_Mutation 1 13695818 A G 7 50 LUAD TCGA-44-2656 PRAMEF18 SNP Missense_Mutation 1 13474988 T C 59 48 OV TCGA-61-1736 PRAMEF18 DEL Frame_Shift_Del 1 13475115 CTCAAGACGGA - 28 61 UCEC TCGA-AP-A051 PRAMEF18 SNP Missense_Mutation 1 13475241 C A 32 49 UCEC TCGA-AP-A056 PRAMEF18 SNP Missense_Mutation 1 13474910 A C 1 44 UCEC TCGA-B5-A11E PRAMEF18 SNP Missense_Mutation 1 13475213 C T 32 39 UCEC TCGA-BS-A0UF PRAMEF18 SNP Missense_Mutation 1 13475258 G T 35 61 HNSC TCGA-CQ-6225 PRAMEF18 SNP Missense_Mutation 1 13475012 G T 35 60 HNSC TCGA-CR-7398 PRAMEF18 DEL Frame_Shift_Del 1 13474788 G - 47 51 HNSC TCGA-CV-5442 PRAMEF18 INS Frame_Shift_Ins 1 13474787 - G 63 58 BLCA TCGA-DK-A1AE PRAMEF18 SNP Silent 1 13475073 C T 32 49