Across TCGA pan-cancer cohorts, SLC33A1 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SLC33A1 data layer compared with 25 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 SLC33A1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SLC33A1 expression acts as an unfavorable survival marker.
CESC, OV, and UCEC are the cancer types where SLC33A1 Mutation most reproducibly stratifies survival.