Across TCGA pan-cancer cohorts, ATP5IF1 Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated ATP5IF1 data layer compared with 27 for mass-spec protein and 6 for mass-spec protein.
The strongest signal is observed in stomach adenocarcinoma (STAD), where higher ATP5IF1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ATP5IF1 expression acts as an unfavorable survival marker.
STAD are the cancer types where ATP5IF1 Mutation most reproducibly stratifies survival.