Across TCGA pan-cancer cohorts, SLC30A7 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SLC30A7 data layer compared with 27 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in liver hepatocellular carcinoma (LIHC), where higher SLC30A7 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SLC30A7 expression acts as an unfavorable survival marker.
LIHC, BRCA, and PRAD are the cancer types where SLC30A7 Mutation most reproducibly stratifies survival.