ClinVar Miner

List of variants in gene DCX reported as pathogenic for Abnormal cortical gyration

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001195553.2(DCX):c.23_24del (p.His7_Phe8insTer) rs797045510
NM_001195553.2(DCX):c.280A>G (p.Asn94Asp) rs797045512
NM_001195553.2(DCX):c.339dup (p.Gly114fs) rs797045514
NM_001195553.2(DCX):c.528del (p.Phe176fs) rs797045515
NM_001195553.2(DCX):c.681dup (p.Leu228fs) rs587783579
NM_001195553.2(DCX):c.685_699dup (p.Tyr229_Gly233dup) rs797045518
NM_001195553.2(DCX):c.81_85dup (p.Pro29fs) rs797045519
NM_001195553.2(DCX):c.875dup (p.Thr293fs) rs797045520
NM_178151.2(DCX):c.226_234delCGTTTTCGCins2

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.