Across TCGA pan-cancer cohorts, SHF Mutation is linked to patient survival in 1 of 34 cancer types, making it a survival-associated SHF data layer compared with 29 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in ovarian serous cystadenocarcinoma (OV), where higher SHF Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SHF expression acts as an unfavorable survival marker.
OV are the cancer types where SHF Mutation most reproducibly stratifies survival.