RAP1A

Across TCGA pan-cancer cohorts, RAP1A Mutation is linked to patient survival in 4 of 34 cancer types, making it a survival-associated RAP1A data layer compared with 21 for mass-spec protein and 5 for mass-spec protein.

The strongest signal is observed in skin cutaneous melanoma (SKCM), where higher RAP1A Mutation is associated with worse disease-free survival. In most high-consensus cancer types, elevated RAP1A expression acts as an unfavorable survival marker, although some lineages such as UCEC show a favorable association.

SKCM, THCA, and CHOL are the cancer types where RAP1A 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
SKCM	DFS	Median	II,III,IV	0.029	0.683	<.001	12	view →
THCA	DFS	Median	All	0.161	0.829	.007	9	view →
CHOL	OS	Median	All	0.155	0.725	.029	3	view →
UCEC	OS	Median	All	1.000	0.662	.045	2	view →

Pink = unfavorable, green = favorable. Showing the 4 strongest of 4 lineages.

RAP1A–SKCM (DFS)

Open the SKCM breakdown →