Across TCGA pan-cancer cohorts, S100A13 Mutation is linked to patient survival in 3 of 34 cancer types, making it a survival-associated S100A13 data layer compared with 23 for mass-spec protein and 6 for mass-spec protein.

The strongest signal is observed in stomach adenocarcinoma (STAD), where higher S100A13 Mutation is associated with worse overall survival. In most high-consensus cancer types, elevated S100A13 expression acts as an unfavorable survival marker.

STAD, COAD, and CHOL are the cancer types where S100A13 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.

Lineage	Measure	Split	Stage	AUC1 high	AUC2 low	p	Sampling consensus
STAD	OS	Median	All	0.003	0.688	<.001	36	view →
COAD	DFS	Median	All	0.074	0.781	<.001	12	view →
CHOL	OS	Median	All	0.155	0.725	.029	3	view →

Pink = unfavorable, green = favorable. Showing the 3 strongest of 3 lineages.

Exploration

Same gene, other analysis: S100A13 tumor-vs-normal RNA expression · all S100A13 data types