Across TCGA pan-cancer cohorts, IFI27L1 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated IFI27L1 data layer compared with 23 for mass-spec protein.
The strongest signal is observed in rectum adenocarcinoma (READ), where higher IFI27L1 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IFI27L1 expression acts as an unfavorable survival marker, although some lineages such as SKCM show a favorable association.
READ and SKCM are the cancer types where IFI27L1 Mutation most reproducibly stratifies survival.