Across TCGA pan-cancer cohorts, LINC00886 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated LINC00886 data layer compared with 23 for mass-spec protein.
The strongest signal is observed in colon adenocarcinoma (COAD), where higher LINC00886 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated LINC00886 expression acts as an unfavorable survival marker.
COAD, LUSC, and UCEC are the cancer types where LINC00886 Mutation most reproducibly stratifies survival.