Across TCGA pan-cancer cohorts, RAB5A Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated RAB5A data layer compared with 24 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher RAB5A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RAB5A expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
CESC, LUAD, and UCEC are the cancer types where RAB5A Mutation most reproducibly stratifies survival.