Across TCGA pan-cancer cohorts, RRAS2 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated RRAS2 data layer compared with 23 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in uterine carcinosarcoma (UCS), where higher RRAS2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RRAS2 expression acts as an unfavorable survival marker.
UCS and PRAD are the cancer types where RRAS2 Mutation most reproducibly stratifies survival.