Across TCGA pan-cancer cohorts, ATP6V0C Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated ATP6V0C data layer compared with 19 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher ATP6V0C Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated ATP6V0C expression acts as an unfavorable survival marker.
SKCM and ACC are the cancer types where ATP6V0C Mutation most reproducibly stratifies survival.