ClinVar Miner

List of variants in gene SCN10A reported as likely benign by GeneDx

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Gene type:
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Total variants: 67
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HGVS dbSNP
NM_006514.3(SCN10A):c.-8A>T rs200901459
NM_006514.3(SCN10A):c.1093-7C>A rs374658847
NM_006514.3(SCN10A):c.1138G>A (p.Val380Ile) rs142276689
NM_006514.3(SCN10A):c.1140A>T (p.Val380=) rs1057523742
NM_006514.3(SCN10A):c.1141A>G (p.Ile381Val) rs150923753
NM_006514.3(SCN10A):c.1197G>A (p.Ala399=) rs759422516
NM_006514.3(SCN10A):c.1233T>A (p.Ile411=) rs144482572
NM_006514.3(SCN10A):c.1249_1251delAAG (p.Lys417del) rs758898721
NM_006514.3(SCN10A):c.1260G>A (p.Glu420=) rs1057524558
NM_006514.3(SCN10A):c.1266C>T (p.Leu422=) rs143438557
NM_006514.3(SCN10A):c.1291-4G>A rs376077984
NM_006514.3(SCN10A):c.1305A>G (p.Leu435=) rs1345381163
NM_006514.3(SCN10A):c.1453C>T (p.Arg485Cys) rs151153639
NM_006514.3(SCN10A):c.1461+19T>A rs199927297
NM_006514.3(SCN10A):c.1518T>C (p.His506=) rs1553620505
NM_006514.3(SCN10A):c.1590C>T (p.His530=) rs770543896
NM_006514.3(SCN10A):c.1661T>C (p.Leu554Pro) rs138404783
NM_006514.3(SCN10A):c.1713G>A (p.Pro571=) rs148905110
NM_006514.3(SCN10A):c.1867+13C>T rs138063699
NM_006514.3(SCN10A):c.1908C>T (p.Thr636=) rs147235762
NM_006514.3(SCN10A):c.1914G>A (p.Leu638=) rs774983974
NM_006514.3(SCN10A):c.1949T>A (p.Met650Lys) rs201698323
NM_006514.3(SCN10A):c.2106+9T>C rs1057524209
NM_006514.3(SCN10A):c.2382G>A (p.Leu794=) rs1057523925
NM_006514.3(SCN10A):c.2475A>C (p.Glu825Asp) rs146028829
NM_006514.3(SCN10A):c.270+12T>C rs761698317
NM_006514.3(SCN10A):c.2703G>A (p.Pro901=) rs142531478
NM_006514.3(SCN10A):c.3585T>C (p.Phe1195=) rs368972137
NM_006514.3(SCN10A):c.3618G>A (p.Val1206=) rs1057523717
NM_006514.3(SCN10A):c.3674T>C (p.Ile1225Thr) rs139638446
NM_006514.3(SCN10A):c.3681+16G>A rs746661487
NM_006514.3(SCN10A):c.3681+9C>T rs201158753
NM_006514.3(SCN10A):c.3705G>A (p.Ala1235=) rs147376215
NM_006514.3(SCN10A):c.372C>T (p.Ile124=) rs575521978
NM_006514.3(SCN10A):c.3805-12A>G rs985392065
NM_006514.3(SCN10A):c.3859G>A (p.Val1287Ile) rs145032037
NM_006514.3(SCN10A):c.390-15A>G rs1057523824
NM_006514.3(SCN10A):c.3990T>G (p.Ser1330=) rs149685953
NM_006514.3(SCN10A):c.39C>T (p.Phe13=) rs181048561
NM_006514.3(SCN10A):c.4089+12A>T rs151164057
NM_006514.3(SCN10A):c.41G>T (p.Arg14Leu) rs141207048
NM_006514.3(SCN10A):c.4282-13G>A rs374834768
NM_006514.3(SCN10A):c.4282-16G>C rs376080236
NM_006514.3(SCN10A):c.4378C>T (p.Arg1460Trp) rs148619598
NM_006514.3(SCN10A):c.4379G>A (p.Arg1460Gln) rs369399424
NM_006514.3(SCN10A):c.4416C>T (p.Ile1472=) rs144944369
NM_006514.3(SCN10A):c.4515G>A (p.Thr1505=) rs191624001
NM_006514.3(SCN10A):c.4568G>A (p.Cys1523Tyr) rs142217269
NM_006514.3(SCN10A):c.4584C>T (p.Phe1528=) rs141828577
NM_006514.3(SCN10A):c.4694G>A (p.Ser1565Asn) rs200063383
NM_006514.3(SCN10A):c.4980G>A (p.Ser1660=) rs544529883
NM_006514.3(SCN10A):c.5295G>A (p.Ser1765=) rs145313578
NM_006514.3(SCN10A):c.5358C>T (p.Ile1786=) rs188413410
NM_006514.3(SCN10A):c.5445C>T (p.Ser1815=) rs111535651
NM_006514.3(SCN10A):c.5496T>C (p.Thr1832=) rs112374164
NM_006514.3(SCN10A):c.5605C>T (p.Arg1869Cys) rs141648641
NM_006514.3(SCN10A):c.5757G>A (p.Pro1919=) rs145340685
NM_006514.3(SCN10A):c.5834A>G (p.Glu1945Gly) rs372702302
NM_006514.3(SCN10A):c.599+9_599+10dup rs750166682
NM_006514.3(SCN10A):c.609C>A (p.Gly203=) rs532353167
NM_006514.3(SCN10A):c.612A>G (p.Thr204=) rs565457429
NM_006514.3(SCN10A):c.648A>C (p.Thr216=) rs150977149
NM_006514.3(SCN10A):c.853G>A (p.Glu285Lys) rs146151670
NM_006514.3(SCN10A):c.87T>C (p.Ala29=) rs148392780
NM_006514.3(SCN10A):c.903G>A (p.Lys301=) rs750691811
NM_006514.3(SCN10A):c.950+17T>C rs188914048
NM_006514.3(SCN10A):c.969T>C (p.Tyr323=) rs143668889

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