ClinVar Miner

List of variants in gene CNTN2 reported as benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NM_005076.5(CNTN2):c.105C>T (p.Phe35=) rs147074435
NM_005076.5(CNTN2):c.1309C>G (p.Leu437Val) rs79431021
NM_005076.5(CNTN2):c.1516C>A (p.Arg506=) rs114903768
NM_005076.5(CNTN2):c.178G>A (p.Ala60Thr) rs12076297
NM_005076.5(CNTN2):c.1896C>T (p.Phe632=) rs145918837
NM_005076.5(CNTN2):c.1969C>T (p.Arg657Trp) rs2305276
NM_005076.5(CNTN2):c.1975A>G (p.Asn659Asp) rs41264871
NM_005076.5(CNTN2):c.2469G>A (p.Gly823=) rs138090348
NM_005076.5(CNTN2):c.2583G>A (p.Ala861=) rs115143667
NM_005076.5(CNTN2):c.2886C>T (p.His962=) rs56111335
NM_005076.5(CNTN2):c.2922T>G (p.Pro974=) rs116036521
NM_005076.5(CNTN2):c.2964G>A (p.Gly988=) rs566959580
NM_005076.5(CNTN2):c.297C>T (p.Asn99=) rs9787172
NM_005076.5(CNTN2):c.63C>T (p.Ser21=) rs149630443
NM_005076.5(CNTN2):c.947C>T (p.Thr316Ile) rs139732336

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.