Across TCGA pan-cancer cohorts, SLC28A2 Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated SLC28A2 data layer compared with 24 for mass-spec protein.
The strongest signal is observed in bladder urothelial carcinoma (BLCA), where higher SLC28A2 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated SLC28A2 expression acts as an unfavorable survival marker, although some lineages such as COAD show a favorable association.
BLCA, GBM, and SKCM are the cancer types where SLC28A2 Mutation most reproducibly stratifies survival.