H3-3A

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, H3-3A Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated H3-3A data layer compared with 23 for mass-spec protein and 2 for mass-spec protein.

The strongest signal is observed in cervical squamous cell carcinoma and endocervical adenocarcinoma (CESC), where higher H3-3A Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated H3-3A expression acts as an unfavorable survival marker.

CESC, LUSC, and DLBC are the cancer types where H3-3A 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
CESCOSMedianIII,IV0.0950.755<.00142view →
LUSCOSMedianAll0.0800.762<.00124view →
DLBCOSMedianAll0.0540.842<.00112view →
LGGOSMedianAll0.2440.801<.0017view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

H3-3A–CESC (OS)

Kaplan–Meier survival curve for H3-3A mutant vs wild-type samples in CESC.

Open the CESC breakdown →

Exploration