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_002977.3(SCN9A):c.*1013C>T rs16851754
NM_002977.3(SCN9A):c.*1118_*1119insCA rs140616949
NM_002977.3(SCN9A):c.*1184T>G rs11902920
NM_002977.3(SCN9A):c.*129C>T rs16851759
NM_002977.3(SCN9A):c.*1492C>G rs73017542
NM_002977.3(SCN9A):c.*1605delT rs148459420
NM_002977.3(SCN9A):c.*1660G>A rs16851753
NM_002977.3(SCN9A):c.*1774G>A rs114843828
NM_002977.3(SCN9A):c.*1796C>T rs16851751
NM_002977.3(SCN9A):c.*2136C>G rs77050817
NM_002977.3(SCN9A):c.*2146G>C rs1062844
NM_002977.3(SCN9A):c.*2154C>G rs17804037
NM_002977.3(SCN9A):c.*2297A>T rs75345520
NM_002977.3(SCN9A):c.*237C>G rs16851755
NM_002977.3(SCN9A):c.*244_*247dupGATT rs143461219
NM_002977.3(SCN9A):c.*2540C>T rs58249489
NM_002977.3(SCN9A):c.*2616_*2626delAACTTTTTTAA rs145255931
NM_002977.3(SCN9A):c.*2640G>A rs13396526
NM_002977.3(SCN9A):c.*2854T>C rs73017538
NM_002977.3(SCN9A):c.*416dupT rs3834910
NM_002977.3(SCN9A):c.*529_*530delCT rs140024416
NM_002977.3(SCN9A):c.*771_*772dupAA rs144515054
NM_002977.3(SCN9A):c.*798dupA rs564394161
NM_002977.3(SCN9A):c.1119T>C (p.Ala373=) rs13414203
NM_002977.3(SCN9A):c.1155G>T (p.Val385=) rs58465962
NM_002977.3(SCN9A):c.1266A>G (p.Glu422=) rs13402180
NM_002977.3(SCN9A):c.1287T>A (p.Arg429=) rs6747673
NM_002977.3(SCN9A):c.1469G>A (p.Ser490Asn) rs58022607
NM_002977.3(SCN9A):c.1942-3dupT rs35888674
NM_002977.3(SCN9A):c.2072-14C>T rs6432893
NM_002977.3(SCN9A):c.2072-15G>A rs4525717
NM_002977.3(SCN9A):c.2841+13delA rs200434162
NM_002977.3(SCN9A):c.2971G>T (p.Val991Leu) rs4369876
NM_002977.3(SCN9A):c.3642C>A (p.Ile1214=) rs77144869
NM_002977.3(SCN9A):c.3769-4A>G rs75230218
NM_002977.3(SCN9A):c.3769-8T>C rs76550960
NM_002977.3(SCN9A):c.4366-10_4366-7delGTTT rs77944059
NM_002977.3(SCN9A):c.4779G>T (p.Val1593=) rs149207258
NM_002977.3(SCN9A):c.5723A>G (p.Asp1908Gly) rs3750904

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