Across TCGA pan-cancer cohorts, CALML3 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated CALML3 data layer compared with 22 for mass-spec protein and 4 for mass-spec protein.
The strongest signal is observed in adrenocortical carcinoma (ACC), where higher CALML3 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated CALML3 expression acts as an unfavorable survival marker.
ACC, LUAD, and PRAD are the cancer types where CALML3 Mutation most reproducibly stratifies survival.