ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as benign for Severe myoclonic epilepsy in infancy

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Total variants: 39
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HGVS dbSNP
NM_001365536.1(SCN9A):c.*1013C>T rs16851754
NM_001365536.1(SCN9A):c.*1118_*1119insCA rs140616949
NM_001365536.1(SCN9A):c.*1184T>G rs11902920
NM_001365536.1(SCN9A):c.*129C>T rs16851759
NM_001365536.1(SCN9A):c.*1492C>G rs73017542
NM_001365536.1(SCN9A):c.*1605del rs148459420
NM_001365536.1(SCN9A):c.*1660G>A rs16851753
NM_001365536.1(SCN9A):c.*1774G>A rs114843828
NM_001365536.1(SCN9A):c.*1796C>T rs16851751
NM_001365536.1(SCN9A):c.*2136C>G rs77050817
NM_001365536.1(SCN9A):c.*2146G>C rs1062844
NM_001365536.1(SCN9A):c.*2154C>G rs17804037
NM_001365536.1(SCN9A):c.*2297A>T rs75345520
NM_001365536.1(SCN9A):c.*237C>G rs16851755
NM_001365536.1(SCN9A):c.*244_*247dup rs143461219
NM_001365536.1(SCN9A):c.*2540C>T rs58249489
NM_001365536.1(SCN9A):c.*2616_*2626del rs145255931
NM_001365536.1(SCN9A):c.*2640G>A rs13396526
NM_001365536.1(SCN9A):c.*2854T>C rs73017538
NM_001365536.1(SCN9A):c.*416dup rs3834910
NM_001365536.1(SCN9A):c.*529_*530del rs140024416
NM_001365536.1(SCN9A):c.*771_*772dup rs144515054
NM_001365536.1(SCN9A):c.*798dup rs564394161
NM_001365536.1(SCN9A):c.1119T>C (p.Ala373=) rs13414203
NM_001365536.1(SCN9A):c.1155G>T (p.Val385=) rs58465962
NM_001365536.1(SCN9A):c.1266A>G (p.Glu422=) rs13402180
NM_001365536.1(SCN9A):c.1287T>A (p.Arg429=) rs6747673
NM_001365536.1(SCN9A):c.1469G>A (p.Ser490Asn) rs58022607
NM_001365536.1(SCN9A):c.1975-12dup rs35888674
NM_001365536.1(SCN9A):c.2105-14C>T rs6432893
NM_001365536.1(SCN9A):c.2105-15G>A rs4525717
NM_001365536.1(SCN9A):c.2874+13del rs200434162
NM_001365536.1(SCN9A):c.3004G>T (p.Val1002Leu) rs4369876
NM_001365536.1(SCN9A):c.3675C>A (p.Ile1225=) rs77144869
NM_001365536.1(SCN9A):c.3802-4A>G rs75230218
NM_001365536.1(SCN9A):c.3802-8T>C rs76550960
NM_001365536.1(SCN9A):c.4399-10_4399-7del rs77944059
NM_001365536.1(SCN9A):c.4812G>T (p.Val1604=) rs149207258
NM_001365536.1(SCN9A):c.5756A>G (p.Asp1919Gly) rs3750904

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