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
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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

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