Across TCGA pan-cancer cohorts, SH2D1A Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated SH2D1A data layer compared with 25 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher SH2D1A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated SH2D1A expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
CESC, UCEC, and BLCA are the cancer types where SH2D1A Mutation most reproducibly stratifies survival.