Across TCGA patient cohorts, IFNA22P mutation is significantly associated with the RNA expression of many other genes, with 56 significant associations in total. SKCM shows the largest number of these associations.

The most reproducible IFNA22P-associated genes across cancer lineages are RN7SL478P, TUBAP1, and ARL6IP1P3. Each is linked with IFNA22P in more than 1 cancer types. Because this analysis shows association rather than direction, both IFNA22P-to-partner and partner-to-IFNA22P results are reported.

Each partner links to its own Q-omics profile.

mutation associated genes by consensus

Ranked by combined sampling and lineage consensus. X-score (IFNA22P→partner) and Y-score (partner→IFNA22P) are standardized regression coefficients; both directions are reported because the association is undirected. p-values are from the association test.

Lineage	Partner gene	X-score	Y-score	p(X)	p(Y)	Sampling consensus	Lineage consensus
SKCM	RN7SL478P →	+0.204	+2.947	<.001	.007	3	2
SKCM	TUBAP1 →	+0.048	+2.893	.002	.006	3	2
SKCM	ARL6IP1P3 →	+0.135	+3.126	<.001	.004	3	2
SKCM	RN7SL784P →	+0.169	+2.976	.001	.006	3	2
SKCM	MTND1P33 →	+0.024	+4.039	<.001	.009	3	1
SKCM	RAC1P7 →	+0.061	+4.039	<.001	.009	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 56 associations by consensus.

Exploration

IFNA22P survival (RNA) · tumor vs normal (RNA) · all IFNA22P data types