Across TCGA pan-cancer cohorts, SAT2 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated SAT2 data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.
The strongest signal is observed in kidney renal papillary cell carcinoma (KIRP), where higher SAT2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SAT2 expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.
KIRP, UCEC, and SKCM are the cancer types where SAT2 Mutation most reproducibly stratifies survival.