ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62686 RMND5A SNP Missense 2 86992290 A G 7 90 LUAD LUAD-S01356 RMND5A SNP Silent 2 86997152 A T 7 52 LUAD TCGA-05-4396 RMND5A SNP Missense_Mutation 2 86980603 C A 21 61 GBM TCGA-06-0648 RMND5A SNP Silent 2 86992995 G A 45 51 OV TCGA-13-0760 RMND5A SNP Missense_Mutation 2 86992174 G C 46 74 LUSC TCGA-33-4586 RMND5A SNP Missense_Mutation 2 86947815 C T 27 66 LUAD TCGA-44-2665 RMND5A SNP Silent 2 86993022 A G 3 52 LUSC TCGA-46-3768 RMND5A SNP Missense_Mutation 2 86980655 G T 35 58 LUAD TCGA-55-1595 RMND5A SNP Silent 2 86992312 A G 1 59 LUAD TCGA-67-3770 RMND5A SNP Missense_Mutation 2 86997154 C G 25 100 UCEC TCGA-AP-A054 RMND5A SNP Translation_Start_Site 2 88019376 C T 19 46 UCEC TCGA-AP-A056 RMND5A SNP Missense_Mutation 2 87000524 T C 49 93 UCEC TCGA-AX-A05Z RMND5A SNP Missense_Mutation 2 86979111 C A 32 59 KIRC TCGA-B0-5703 RMND5A SNP Silent 2 86980658 C T 29 61 UCEC TCGA-BG-A0VZ RMND5A DEL Frame_Shift_Del 2 86997177 TTAA - 64 52 UCEC TCGA-BS-A0UF RMND5A SNP Missense_Mutation 2 86968107 G T 33 81 BLCA TCGA-CF-A27C RMND5A SNP Missense_Mutation 2 86992169 G A 41 82 BLCA TCGA-CF-A27C RMND5A SNP Missense_Mutation 2 86992260 G A 37 74 HNSC TCGA-CV-5443 RMND5A SNP Missense_Mutation 2 86947840 A T 3 76 BRCA TCGA-D8-A1JC RMND5A SNP Missense_Mutation 2 86993049 C A 18 66