List of variants in gene COQ8B reported as uncertain significance for Nephrotic syndrome, type 9

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_024876.4(COQ8B):c.1297-6T>G	rs199934542	0.00056
NM_024876.4(COQ8B):c.953C>T (p.Thr318Met)	rs55899516	0.00018
NM_024876.4(COQ8B):c.826G>C (p.Ala276Pro)	rs200480831	0.00016
NM_024876.4(COQ8B):c.1035+3A>G	rs368182892	0.00009
NM_024876.4(COQ8B):c.1391G>A (p.Arg464His)	rs185934352	0.00009
NM_024876.4(COQ8B):c.737G>A (p.Ser246Asn)	rs200841458	0.00004
NM_024876.4(COQ8B):c.1186G>A (p.Glu396Lys)	rs1318617277	0.00001
NM_024876.4(COQ8B):c.1552C>T (p.Arg518Cys)	rs746915084	0.00001
NM_024876.4(COQ8B):c.116G>T (p.Gly39Val)
NM_024876.4(COQ8B):c.1459G>T (p.Ala487Ser)
NM_024876.4(COQ8B):c.1465C>T (p.His489Tyr)
NM_024876.4(COQ8B):c.451G>A (p.Gly151Arg)
NM_024876.4(COQ8B):c.538C>T (p.Arg180Cys)	rs866812916
NM_024876.4(COQ8B):c.748G>C (p.Asp250His)	rs769834604
NM_024876.4(COQ8B):c.853T>C (p.Cys285Arg)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.