Across TCGA pan-cancer cohorts, MIR548H4 Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated MIR548H4 data layer compared with 3 for mass-spec protein.
The strongest signal is observed in cholangiocarcinoma (CHOL), where higher MIR548H4 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated MIR548H4 expression acts as an unfavorable survival marker.
CHOL are the cancer types where MIR548H4 Mutation most reproducibly stratifies survival.