IGHV3-30

Mutation & survival
SurvivalMutationKaplan–Meier · TCGA cohorts

Across TCGA pan-cancer cohorts, IGHV3-30 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated IGHV3-30 data layer compared with 25 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in lymphoid neoplasm diffuse large b-cell lymphoma (DLBC), where higher IGHV3-30 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated IGHV3-30 expression acts as an unfavorable survival marker.

DLBC, LUAD, and LUSC are the cancer types where IGHV3-30 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
DLBCOSMedianII,III,IV0.1180.802.02512view →
LUADOSMedianAll0.2580.812.00412view →
LUSCOSMedianAll0.1960.659.0453view →
Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

IGHV3-30–DLBC (OS)

Kaplan–Meier survival curve for IGHV3-30 mutant vs wild-type samples in DLBC.

Open the DLBC breakdown →

Exploration