ClinVar Miner

List of variants in gene SCN2A reported as likely benign for Benign familial neonatal-infantile seizures

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Total variants: 22
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HGVS dbSNP
NM_001040142.1(SCN2A):c.*2490G>A rs189308010
NM_001040142.2(SCN2A):c.*2480A>G
NM_001040142.2(SCN2A):c.*792A>G rs539290679
NM_001040142.2(SCN2A):c.*874A>G
NM_001040142.2(SCN2A):c.122G>A (p.Arg41His)
NM_001040142.2(SCN2A):c.1542T>C (p.Ser514=)
NM_001040142.2(SCN2A):c.1725G>A (p.Ala575=) rs543538780
NM_001040142.2(SCN2A):c.1759A>C (p.Ile587Leu) rs148275498
NM_001040142.2(SCN2A):c.2005C>T (p.Leu669Phe)
NM_001040142.2(SCN2A):c.2046G>T (p.Lys682Asn) rs756493732
NM_001040142.2(SCN2A):c.2051G>A (p.Arg684Gln) rs146949852
NM_001040142.2(SCN2A):c.2157A>G (p.Glu719=) rs779574574
NM_001040142.2(SCN2A):c.2723A>G (p.Lys908Arg) rs2228980
NM_001040142.2(SCN2A):c.2923C>T (p.Leu975=) rs375858093
NM_001040142.2(SCN2A):c.3457G>A (p.Glu1153Lys) rs200138205
NM_001040142.2(SCN2A):c.3735T>C (p.Ala1245=) rs527970192
NM_001040142.2(SCN2A):c.4287T>C (p.Tyr1429=) rs150209984
NM_001040142.2(SCN2A):c.4565G>C (p.Gly1522Ala) rs147522594
NM_001040142.2(SCN2A):c.5155T>C (p.Leu1719=) rs199698414
NM_001040142.2(SCN2A):c.5397T>C (p.Tyr1799=) rs200603552
NM_001040142.2(SCN2A):c.5544T>C (p.Ser1848=) rs761713186
NM_001040142.2(SCN2A):c.681A>G (p.Thr227=)

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