Across TCGA pan-cancer cohorts, RPL7L1 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RPL7L1 data layer compared with 26 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in breast invasive carcinoma (BRCA), where higher RPL7L1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated RPL7L1 expression acts as an unfavorable survival marker.
BRCA, STAD, and UCEC are the cancer types where RPL7L1 Mutation most reproducibly stratifies survival.