ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as benign

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Gene type:
ClinVar version:
Total variants: 78
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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.*1605del 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_*247dup rs143461219
NM_002977.3(SCN9A):c.*2540C>T rs58249489
NM_002977.3(SCN9A):c.*2616_*2626del rs145255931
NM_002977.3(SCN9A):c.*2640G>A rs13396526
NM_002977.3(SCN9A):c.*2854T>C rs73017538
NM_002977.3(SCN9A):c.*416dup rs3834910
NM_002977.3(SCN9A):c.*529_*530del rs140024416
NM_002977.3(SCN9A):c.*771_*772dup rs144515054
NM_002977.3(SCN9A):c.*798dup 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.1326G>A (p.Ala442=) rs200065104
NM_002977.3(SCN9A):c.1398C>T (p.Ser466=) rs201531206
NM_002977.3(SCN9A):c.1469G>A (p.Ser490Asn) rs58022607
NM_002977.3(SCN9A):c.1828C>A (p.Pro610Thr) rs41268673
NM_002977.3(SCN9A):c.1838C>T (p.Pro613Leu) rs200671761
NM_002977.3(SCN9A):c.1942-12dup rs35888674
NM_002977.3(SCN9A):c.1942-3del rs35888674
NM_002977.3(SCN9A):c.1964A>G (p.Lys655Arg) rs121908919
NM_002977.3(SCN9A):c.2072-14C>T rs6432893
NM_002977.3(SCN9A):c.2072-15G>A rs4525717
NM_002977.3(SCN9A):c.2157G>C (p.Trp719Cys) rs202055175
NM_002977.3(SCN9A):c.2215A>G (p.Ile739Val) rs182650126
NM_002977.3(SCN9A):c.2311-20A>T rs199905079
NM_002977.3(SCN9A):c.2359A>G (p.Met787Val) rs149707354
NM_002977.3(SCN9A):c.2376T>C (p.Tyr792=) rs142219317
NM_002977.3(SCN9A):c.2404A>G (p.Ser802Gly) rs201890240
NM_002977.3(SCN9A):c.2484+6C>T rs145316463
NM_002977.3(SCN9A):c.2700C>T (p.Asn900=) rs201560403
NM_002977.3(SCN9A):c.2733C>T (p.Arg911=) rs199653503
NM_002977.3(SCN9A):c.2794A>C (p.Met932Leu) rs12478318
NM_002977.3(SCN9A):c.2820C>G (p.Val940=) rs764006250
NM_002977.3(SCN9A):c.2841+13del rs200434162
NM_002977.3(SCN9A):c.2971G>T (p.Val991Leu) rs4369876
NM_002977.3(SCN9A):c.3018G>C (p.Lys1006Asn) rs147623238
NM_002977.3(SCN9A):c.3162C>T (p.Ser1054=) rs111674454
NM_002977.3(SCN9A):c.3255C>T (p.Ser1085=) rs749337119
NM_002977.3(SCN9A):c.3328C>T (p.Arg1110Trp) rs190664764
NM_002977.3(SCN9A):c.3329G>A (p.Arg1110Gln) rs74401238
NM_002977.3(SCN9A):c.3369G>T (p.Leu1123Phe) rs200160858
NM_002977.3(SCN9A):c.3448= (p.Arg1150=) rs6746030
NM_002977.3(SCN9A):c.3448C>T (p.Arg1150Trp) rs6746030
NM_002977.3(SCN9A):c.3473A>C (p.Asn1158Thr) rs151241025
NM_002977.3(SCN9A):c.3642C>A (p.Ile1214=) rs77144869
NM_002977.3(SCN9A):c.3651T>C (p.Tyr1217=) rs144941725
NM_002977.3(SCN9A):c.3734A>G (p.Asn1245Ser) rs141268327
NM_002977.3(SCN9A):c.3769-4A>G rs75230218
NM_002977.3(SCN9A):c.3769-8T>C rs76550960
NM_002977.3(SCN9A):c.4077T>C (p.Cys1359=) rs199673396
NM_002977.3(SCN9A):c.4143C>T (p.Val1381=) rs558455181
NM_002977.3(SCN9A):c.4281C>T (p.Val1427=) rs188336294
NM_002977.3(SCN9A):c.4323C>T (p.Phe1441=) rs201145311
NM_002977.3(SCN9A):c.4366-10_4366-7delGTTT rs77944059
NM_002977.3(SCN9A):c.4366-14G>T rs112927502
NM_002977.3(SCN9A):c.4366-17_4366-16insA rs569037217
NM_002977.3(SCN9A):c.4612T>C (p.Trp1538Arg) rs202084411
NM_002977.3(SCN9A):c.4741+16T>A rs10180721
NM_002977.3(SCN9A):c.4779G>T (p.Val1593=) rs149207258
NM_002977.3(SCN9A):c.4890T>C (p.Leu1630=) rs199550149
NM_002977.3(SCN9A):c.5678G>A (p.Arg1893His) rs79805025
NM_002977.3(SCN9A):c.5723A>G (p.Asp1908Gly) rs3750904
NM_002977.3(SCN9A):c.5746C>T (p.Leu1916Phe) rs111558968

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