Across TCGA pan-cancer cohorts, EIF3H Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated EIF3H data layer compared with 25 for mass-spec protein and 7 for mass-spec protein.
The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher EIF3H Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated EIF3H expression acts as an unfavorable survival marker.
SKCM, CHOL, and LIHC are the cancer types where EIF3H Mutation most reproducibly stratifies survival.