Across TCGA pan-cancer cohorts, RHOV Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated RHOV data layer compared with 23 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher RHOV Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RHOV expression acts as an unfavorable survival marker.
CESC and HNSC are the cancer types where RHOV Mutation most reproducibly stratifies survival.