ClinVar Miner

List of variants in gene SCN2B reported as likely benign for Atrial fibrillation, familial, 14

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Total variants: 17
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HGVS dbSNP
NM_004588.5(SCN2B):c.126T>C (p.Asn42=)
NM_004588.5(SCN2B):c.129C>T (p.Gly43=) rs150955748
NM_004588.5(SCN2B):c.150C>T (p.Cys50=) rs751437266
NM_004588.5(SCN2B):c.238-6C>T rs200842493
NM_004588.5(SCN2B):c.324C>T (p.Tyr108=)
NM_004588.5(SCN2B):c.340C>T (p.Leu114=) rs961380475
NM_004588.5(SCN2B):c.348C>T (p.Asn116=) rs72544144
NM_004588.5(SCN2B):c.354G>A (p.Gln118=)
NM_004588.5(SCN2B):c.357G>A (p.Pro119=) rs149169244
NM_004588.5(SCN2B):c.39C>T (p.Ser13=) rs772656576
NM_004588.5(SCN2B):c.470C>T (p.Thr157Met) rs760333798
NM_004588.5(SCN2B):c.495C>T (p.Ser165=)
NM_004588.5(SCN2B):c.561A>G (p.Lys187=)
NM_004588.5(SCN2B):c.594C>T (p.Thr198=)
NM_004588.5(SCN2B):c.615C>T (p.Asp205=) rs201971719
NM_004588.5(SCN2B):c.630G>A (p.Pro210=)
NM_004588.5(SCN2B):c.639C>T (p.Gly213=)

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