Across TCGA pan-cancer cohorts, CYP27C1 Mutation is linked to patient survival in 2 of 34 cancer types, making it a survival-associated CYP27C1 data layer compared with 25 for mass-spec protein and 1 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher CYP27C1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated CYP27C1 expression acts as an unfavorable survival marker.
COAD and HNSC are the cancer types where CYP27C1 Mutation most reproducibly stratifies survival.