H3-3B

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, H3-3B Mutation is linked to patient survival in 5 of 34 cancer types, making it a survival-associated H3-3B data layer compared with 22 for mass-spec protein.

The strongest signal is observed in lung adenocarcinoma (LUAD), where higher H3-3B Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated H3-3B expression acts as an unfavorable survival marker.

LUAD, MESO, and CHOL are the cancer types where H3-3B 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
LUADOSMedianAll0.3370.837<.00118view →
MESODFSMedianII,III,IV0.0390.407<.00112view →
CHOLOSMedianAll0.1550.725.0293view →
LUSCOSMedianII,III,IV0.2790.732.0383view →
SKCMDFSMedianII,III,IV0.1000.235.0421view →
Pink = unfavorable, green = favorable. Showing the 5 strongest of 5 lineages.

H3-3B–LUAD (OS)

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

Open the LUAD breakdown →

Exploration