Across TCGA pan-cancer cohorts, SH2D4B Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated SH2D4B data layer compared with 19 for mass-spec protein.
The strongest signal is observed in breast invasive carcinoma (BRCA), where higher SH2D4B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SH2D4B expression acts as an unfavorable survival marker, although some lineages such as SKCM and UCEC show a favorable association.
BRCA, BLCA, and SKCM are the cancer types where SH2D4B Mutation most reproducibly stratifies survival.