Across TCGA pan-cancer cohorts, RPS3A Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RPS3A data layer compared with 22 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in lung adenocarcinoma (LUAD), where higher RPS3A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RPS3A expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
LUAD, UCEC, and SKCM are the cancer types where RPS3A Mutation most reproducibly stratifies survival.