Across TCGA pan-cancer cohorts, RPS10 Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated RPS10 data layer compared with 27 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher RPS10 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RPS10 expression acts as an unfavorable survival marker.
CESC are the cancer types where RPS10 Mutation most reproducibly stratifies survival.