NSMAF

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, NSMAF Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated NSMAF data layer compared with 23 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in breast invasive carcinoma (BRCA), where higher NSMAF Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated NSMAF expression acts as an unfavorable survival marker, although some lineages such as UCEC and BLCA show a favorable association.

BRCA, UCEC, and SARC are the cancer types where NSMAF Mutation most reproducibly stratifies survival.

Mutation survival associations by lineage

Ranked by sampling consensus. AUC1 and AUC2 indicate survival in the high- and low-expression groups, respectively; the lower AUC marks the poorer-surviving group. p-values are from the log-rank test.
LineageMeasureSplitStageAUC1
high
AUC2
low
pSampling consensus
BRCAOSMedianIII,IV0.1060.906<.00126view →
UCECDFSMedianAll0.9650.625.01510view →
SARCOSMedianAll0.1260.860<.0016view →
BLCADFSMedianII,III,IV0.7420.324.0414view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

NSMAF–BRCA (OS)

Kaplan–Meier survival curve for NSMAF mutant vs wild-type samples in BRCA.

Open the BRCA breakdown →

Exploration