ClinVar Miner

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

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Total variants: 40
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HGVS dbSNP
NM_001040142.1(SCN2A):c.*2490G>A rs189308010
NM_021007.2(SCN2A):c.*1474G>A rs138232803
NM_021007.2(SCN2A):c.*1507T>G rs149580267
NM_021007.2(SCN2A):c.*1753C>T rs74881341
NM_021007.2(SCN2A):c.*2039A>G rs554913735
NM_021007.2(SCN2A):c.*2222G>A rs187365022
NM_021007.2(SCN2A):c.*2358A>C rs191911206
NM_021007.2(SCN2A):c.*2364T>G rs73969402
NM_021007.2(SCN2A):c.*2422G>T rs73972503
NM_021007.2(SCN2A):c.*2423A>G rs77976453
NM_021007.2(SCN2A):c.*2440C>G rs73972504
NM_021007.2(SCN2A):c.*417C>T rs141754622
NM_021007.2(SCN2A):c.*557G>A rs182846824
NM_021007.2(SCN2A):c.*792A>G rs539290679
NM_021007.2(SCN2A):c.*853C>T rs188104763
NM_021007.2(SCN2A):c.*88G>A rs574867892
NM_021007.2(SCN2A):c.100G>A (p.Ala34Thr) rs144814658
NM_021007.2(SCN2A):c.1269G>A (p.Val423=) rs139815570
NM_021007.2(SCN2A):c.1725G>A (p.Ala575=) rs543538780
NM_021007.2(SCN2A):c.1785T>C (p.Asp595=) rs141815642
NM_021007.2(SCN2A):c.1842G>T (p.Pro614=) rs114315466
NM_021007.2(SCN2A):c.1959G>A (p.Val653=) rs200546427
NM_021007.2(SCN2A):c.2034A>G (p.Thr678=) rs147891446
NM_021007.2(SCN2A):c.24G>A (p.Pro8=) rs149534277
NM_021007.2(SCN2A):c.2723A>G (p.Lys908Arg) rs2228980
NM_021007.2(SCN2A):c.2955C>T (p.Ser985=) rs149859004
NM_021007.2(SCN2A):c.3123G>A (p.Pro1041=) rs147576541
NM_021007.2(SCN2A):c.3213A>C (p.Gly1071=) rs199997352
NM_021007.2(SCN2A):c.3372C>T (p.Ser1124=) rs571408286
NM_021007.2(SCN2A):c.3453C>T (p.Pro1151=) rs145662546
NM_021007.2(SCN2A):c.3594G>A (p.Arg1198=) rs140194137
NM_021007.2(SCN2A):c.3735T>C (p.Ala1245=) rs527970192
NM_021007.2(SCN2A):c.4565G>C (p.Gly1522Ala) rs147522594
NM_021007.2(SCN2A):c.4989C>T (p.Ile1663=) rs373347369
NM_021007.2(SCN2A):c.5229A>G (p.Lys1743=) rs2227898
NM_021007.2(SCN2A):c.5364G>A (p.Glu1788=) rs199925238
NM_021007.2(SCN2A):c.5517C>T (p.Leu1839=) rs148424455
NM_021007.2(SCN2A):c.5910G>A (p.Thr1970=) rs75057869
NM_021007.2(SCN2A):c.5931T>C (p.Ser1977=) rs187728892
NM_021007.2(SCN2A):c.960T>C (p.Ile320=) rs185590667

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