Across TCGA pan-cancer cohorts, CCDC102A Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated CCDC102A data layer compared with 24 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in stomach adenocarcinoma (STAD), where higher CCDC102A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated CCDC102A expression acts as an unfavorable survival marker.
STAD, LIHC, and UCEC are the cancer types where CCDC102A Mutation most reproducibly stratifies survival.