ClinVar Miner

List of variants in gene SCN10A reported as benign

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Gene type:
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Total variants: 73
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HGVS dbSNP
NM_006514.3(SCN10A):c.1157T>G (p.Phe386Cys) rs78555408
NM_006514.3(SCN10A):c.1284G>A (p.Glu428=) rs62244070
NM_006514.3(SCN10A):c.1290+237G>A rs7374030
NM_006514.3(SCN10A):c.1291-4G>A rs376077984
NM_006514.3(SCN10A):c.1291-5C>T rs563934615
NM_006514.3(SCN10A):c.1453C>T (p.Arg485Cys) rs151153639
NM_006514.3(SCN10A):c.1461+294T>C rs12630795
NM_006514.3(SCN10A):c.1462-265A>G rs7431144
NM_006514.3(SCN10A):c.1476C>T (p.Leu492=) rs7617919
NM_006514.3(SCN10A):c.1525T>C (p.Ser509Pro) rs7630989
NM_006514.3(SCN10A):c.1768G>A (p.Gly590Arg) rs35332705
NM_006514.3(SCN10A):c.1867+57G>A rs12054245
NM_006514.3(SCN10A):c.1867+82G>A rs12494065
NM_006514.3(SCN10A):c.1868-118A>C rs72866265
NM_006514.3(SCN10A):c.1868-208A>C rs72866266
NM_006514.3(SCN10A):c.1868-36T>G rs7618620
NM_006514.3(SCN10A):c.1868-9A>G rs6599250
NM_006514.3(SCN10A):c.1949T>A (p.Met650Lys) rs201698323
NM_006514.3(SCN10A):c.2043C>T (p.Phe681=) rs367743519
NM_006514.3(SCN10A):c.2106+44C>T rs72866260
NM_006514.3(SCN10A):c.2280+263T>C rs73826310
NM_006514.3(SCN10A):c.2280+298C>T rs72866253
NM_006514.3(SCN10A):c.2281-247G>C rs7433306
NM_006514.3(SCN10A):c.2640+170G>T rs75284873
NM_006514.3(SCN10A):c.2641-95C>G rs73825883
NM_006514.3(SCN10A):c.268C>T (p.Arg90Trp) rs144270136
NM_006514.3(SCN10A):c.270+133A>T rs79414348
NM_006514.3(SCN10A):c.285G>T (p.Leu95=) rs560088419
NM_006514.3(SCN10A):c.3508-189G>T rs6805187
NM_006514.3(SCN10A):c.3542C>T (p.Thr1181Met) rs150773437
NM_006514.3(SCN10A):c.3682-206A>T rs6796459
NM_006514.3(SCN10A):c.3682-329T>C rs61014925
NM_006514.3(SCN10A):c.3682-66T>C rs6793226
NM_006514.3(SCN10A):c.3805-156C>T rs7372672
NM_006514.3(SCN10A):c.3805-240A>G rs62242430
NM_006514.3(SCN10A):c.3805-41G>A rs6781740
NM_006514.3(SCN10A):c.390-9G>A rs370917734
NM_006514.3(SCN10A):c.4009T>A (p.Ser1337Thr) rs11711062
NM_006514.3(SCN10A):c.4090-19C>T rs77494117
NM_006514.3(SCN10A):c.4282-152A>T rs6599248
NM_006514.3(SCN10A):c.4282-165G>A rs78376096
NM_006514.3(SCN10A):c.4323A>G (p.Lys1441=) rs6790627
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.45C>T (p.Arg15=) rs34314583
NM_006514.3(SCN10A):c.462G>A (p.Glu154=) rs541804553
NM_006514.3(SCN10A):c.4656G>A (p.Ala1552=) rs151182542
NM_006514.3(SCN10A):c.4657+16C>T rs115824540
NM_006514.3(SCN10A):c.4680T>G (p.Leu1560=) rs529845623
NM_006514.3(SCN10A):c.4694G>A (p.Ser1565Asn) rs200063383
NM_006514.3(SCN10A):c.471-111A>G rs62244081
NM_006514.3(SCN10A):c.4710G>A (p.Thr1570=) rs78425180
NM_006514.3(SCN10A):c.4866T>C (p.Ser1622=) rs6599242
NM_006514.3(SCN10A):c.4872C>T (p.Phe1624=) rs149642957
NM_006514.3(SCN10A):c.4984G>A (p.Gly1662Ser) rs151090729
NM_006514.3(SCN10A):c.5047C>T (p.Pro1683Ser) rs146999807
NM_006514.3(SCN10A):c.5089G>A (p.Val1697Ile) rs77804526
NM_006514.3(SCN10A):c.5137= (p.Val1713=) rs6599241
NM_006514.3(SCN10A):c.5137G>A (p.Val1713Met) rs6599241
NM_006514.3(SCN10A):c.5217C>T (p.Asp1739=) rs116353929
NM_006514.3(SCN10A):c.5295G>A (p.Ser1765=) rs145313578
NM_006514.3(SCN10A):c.53C>T (p.Pro18Leu) rs190176472
NM_006514.3(SCN10A):c.5496T>C (p.Thr1832=) rs112374164
NM_006514.3(SCN10A):c.5628C>G (p.Thr1876=) rs147660344
NM_006514.3(SCN10A):c.5657C>T (p.Ala1886Val) rs142653846
NM_006514.3(SCN10A):c.5834A>G (p.Glu1945Gly) rs372702302
NM_006514.3(SCN10A):c.599+120C>T rs10212338
NM_006514.3(SCN10A):c.600-43G>C rs73826327
NM_006514.3(SCN10A):c.618A>G (p.Ile206Met) rs74717885
NM_006514.3(SCN10A):c.648A>C (p.Thr216=) rs150977149
NM_006514.3(SCN10A):c.884-13T>C rs7641844
NM_006514.3(SCN10A):c.951-186G>A rs6798015

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