Across TCGA pan-cancer cohorts, MIR548I4 Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated MIR548I4 data layer compared with 6 for mass-spec protein.
The strongest signal is observed in mesothelioma (MESO), where higher MIR548I4 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated MIR548I4 expression acts as an unfavorable survival marker.
MESO are the cancer types where MIR548I4 Mutation most reproducibly stratifies survival.