List of variants in gene CARD14, LOC126862662, SGSH studied for Autoinflammatory syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001366385.1(CARD14):c.2458C>T (p.Arg820Trp)	rs11652075	0.39960
NM_001366385.1(CARD14):c.2409G>A (p.Thr803=)	rs115102551	0.00689
NM_001366385.1(CARD14):c.2496C>T (p.Leu832=)	rs139789664	0.00506
NM_001366385.1(CARD14):c.2648G>A (p.Arg883His)	rs2289541	0.00267
NM_001366385.1(CARD14):c.2569+4T>C	rs146678380	0.00181
NM_001366385.1(CARD14):c.2403C>T (p.Ser801=)	rs189286068	0.00026
NM_001366385.1(CARD14):c.2476C>T (p.Arg826Trp)	rs139467141	0.00018
NM_001366385.1(CARD14):c.2641G>A (p.Gly881Arg)	rs548495951	0.00002
NM_001366385.1(CARD14):c.2473G>A (p.Ala825Thr)	rs538251591	0.00001
NM_001366385.1(CARD14):c.2517G>C (p.Lys839Asn)	rs950950885	0.00001
NM_001366385.1(CARD14):c.2535G>A (p.Leu845=)	rs1193362044	0.00001
NM_001366385.1(CARD14):c.2579G>T (p.Ser860Ile)	rs865872056	0.00001
NM_001366385.1(CARD14):c.2638T>C (p.Ser880Pro)	rs754405150	0.00001
NM_001366385.1(CARD14):c.2591A>G (p.Tyr864Cys)	rs1196800518

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.