H3C1

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, H3C1 Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated H3C1 data layer compared with 22 for mass-spec protein.

The strongest signal is observed in lung squamous cell carcinoma (LUSC), where higher H3C1 Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated H3C1 expression acts as an unfavorable survival marker.

LUSC, COAD, and ACC are the cancer types where H3C1 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
LUSCDFSMedianII,III,IV0.1350.663.0159view →
COADOSMedianAll0.1130.806<.0016view →
ACCOSMedianAll0.1180.624.0386view →
LUADOSMedianAll0.2410.684.0373view →
Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

H3C1–LUSC (DFS)

Kaplan–Meier survival curve for H3C1 mutant vs wild-type samples in LUSC.

Open the LUSC breakdown →

Exploration