ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-106 RHOG SNP Silent 11 3848964 C T 27 44 MM MM-0608 RHOG SNP Missense_Mutation 11 3849123 G C 33 75 GBM TCGA-12-0692 RHOG SNP Silent 11 3849147 C T 32 74 OV TCGA-24-2271 RHOG SNP Missense 11 3849245 C A 27 72 UCEC TCGA-A5-A0GP RHOG SNP Missense_Mutation 11 3849290 C T 27 76 UCEC TCGA-AP-A051 RHOG SNP Silent 11 3849087 C T 26 63 UCEC TCGA-B5-A11E RHOG SNP Missense_Mutation 11 3848963 G A 42 83 HNSC TCGA-BA-5149 RHOG SNP Missense_Mutation 11 3848803 A C 12 73 UCEC TCGA-BG-A0M2 RHOG SNP Silent 11 3849021 C T 32 82 UCEC TCGA-D1-A160 RHOG SNP Missense_Mutation 11 3849260 A G 2 89 UCEC TCGA-D1-A17A RHOG SNP Missense_Mutation 11 3848954 G A 44 72