Across TCGA pan-cancer cohorts, SCAMP3 Mutation is linked to patient survival in 6 of 34 cancer types, making it a survival-associated SCAMP3 data layer compared with 25 for mass-spec protein and 7 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher SCAMP3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SCAMP3 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
CESC, ESCA, and UCEC are the cancer types where SCAMP3 Mutation most reproducibly stratifies survival.