Across TCGA pan-cancer cohorts, SVOP Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SVOP data layer compared with 23 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in breast invasive carcinoma (BRCA), where higher SVOP Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SVOP expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
BRCA, KICH, and UCEC are the cancer types where SVOP Mutation most reproducibly stratifies survival.