ClinVar Miner

List of variants in gene SPAG1 studied for autosomal dominant nocturnal frontal lobe epilepsy

Included ClinVar conditions (8):

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: 3

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003114.5(SPAG1):c.2014C>T (p.Gln672Ter)	rs201740530	0.00010
NM_003114.5(SPAG1):c.2542del (p.Asp848fs)	rs886037653
NM_003114.5(SPAG1):c.679G>T (p.Glu227Ter)	rs397518459

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.