Across TCGA pan-cancer cohorts, SFXN3 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated SFXN3 data layer compared with 28 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher SFXN3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SFXN3 expression acts as an unfavorable survival marker.
SKCM and UCEC are the cancer types where SFXN3 Mutation most reproducibly stratifies survival.