ClinVar Miner

List of variants in gene NHLRC1 reported as benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (88):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
NM_198586.3(NHLRC1):c.*237T>C rs73379118
NM_198586.3(NHLRC1):c.*276G>C rs11966748
NM_198586.3(NHLRC1):c.*336G>A rs10949482
NM_198586.3(NHLRC1):c.*344A>T rs147528518
NM_198586.3(NHLRC1):c.*482C>G rs114713758
NM_198586.3(NHLRC1):c.*55G>C rs11966789
NM_198586.3(NHLRC1):c.*621T>A rs10949481
NM_198586.3(NHLRC1):c.*626C>T rs10949480
NM_198586.3(NHLRC1):c.*85T>A rs73379121
NM_198586.3(NHLRC1):c.303G>T (p.Pro101=) rs187783545
NM_198586.3(NHLRC1):c.312T>C (p.His104=) rs115931931
NM_198586.3(NHLRC1):c.32C>A (p.Ala11Glu) rs139029314
NM_198586.3(NHLRC1):c.332C>T (p.Pro111Leu) rs10949483
NM_198586.3(NHLRC1):c.969C>T (p.Ser323=) rs142941035

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.