ClinVar Miner

List of variants in gene CHRNA4 reported as likely benign for Autosomal dominant nocturnal frontal lobe epilepsy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NM_000744.6(CHRNA4):c.105C>T (p.His35=) rs199541666
NM_000744.6(CHRNA4):c.1083G>A (p.Pro361=) rs202140852
NM_000744.6(CHRNA4):c.1104C>T (p.Cys368=) rs202166947
NM_000744.6(CHRNA4):c.132C>T (p.Leu44=) rs1555840462
NM_000744.6(CHRNA4):c.1527C>T (p.Ala509=) rs758693290
NM_000744.6(CHRNA4):c.1726G>C (p.Asp576His) rs537904499
NM_000744.6(CHRNA4):c.372C>T (p.Val124=) rs201386851
NM_000744.6(CHRNA4):c.77-10C>T rs200490160
NM_000744.6(CHRNA4):c.777C>T (p.Cys259=) rs1555837947
NM_000744.6(CHRNA4):c.912A>G (p.Pro304=) rs1041716120

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.