ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-191 RHOD SNP Silent 11 66839013 C T 29 50 ESO ESO-708 RHOD SNP Missense_Mutation 11 66839030 A G 2 52 LUAD LUAD-CHTN-3090346 RHOD SNP Missense_Mutation 11 66838933 G T 38 71 LUAD LUAD-RT-S01813 RHOD DNP Missense_Mutation 11 66839064 GG TA 47 60 MEL MEL-Ma-Mel-114 RHOD SNP Missense_Mutation 11 66838930 G A 43 55 LUAD TCGA-05-4432 RHOD SNP Missense_Mutation 11 66837915 A G 8 70 GBM TCGA-16-1048 RHOD SNP Splice_site 11 66839075 C A 27 30 LUAD TCGA-44-3398 RHOD SNP Silent 11 66834240 G T 48 49 LUAD TCGA-64-5778 RHOD SNP Silent 11 66833438 C T 17 44 UCEC TCGA-AX-A0J1 RHOD SNP Missense_Mutation 11 66837972 A G 10 70 HNSC TCGA-CV-7245 RHOD SNP Missense_Mutation 11 66834226 C T 23 74