Across TCGA patient cohorts, SNORA3C mutation is significantly associated with the RNA expression of many other genes, with 42 significant associations in total. UCEC shows the largest number of these associations.

The most reproducible SNORA3C-associated genes across cancer lineages are RNU6-1300P, RPL23AP68, and TBC1D3F. Each is linked with SNORA3C in more than 1 cancer types. Because this analysis shows association rather than direction, both SNORA3C-to-partner and partner-to-SNORA3C 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 (SNORA3C→partner) and Y-score (partner→SNORA3C) 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
COAD	RNU6-1300P →	+0.462	+5.212	.002	.007	3	1
COAD	RPL23AP68 →	+0.140	+5.357	<.001	.006	3	1
COAD	TBC1D3F →	+0.020	+5.017	.002	.009	3	1
COAD	FAM25C →	+0.356	+5.357	<.001	.006	3	1
UCEC	LINC01670 →	+0.075	+2.995	.003	.005	3	1
UCEC	RNU1-17P →	+0.275	+3.198	.001	.009	3	1

Each partner links to its Q-omics profile. Showing the 6 strongest of 42 associations by consensus.

Exploration

SNORA3C survival (RNA) · tumor vs normal (RNA) · all SNORA3C data types