ClinVar Miner

List of variants in gene SCN10A reported as benign by GeneDx

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Gene type:
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Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_006514.4(SCN10A):c.5137A>G (p.Met1713Val) rs6599241 1.00000
NM_006514.4(SCN10A):c.4866T>C (p.Ser1622=) rs6599242 0.93283
NM_006514.4(SCN10A):c.4282-152A>T rs6599248 0.82340
NM_006514.4(SCN10A):c.951-186G>A rs6798015 0.70024
NM_006514.4(SCN10A):c.2281-247G>C rs7433306 0.69924
NM_006514.4(SCN10A):c.1868-9A>G rs6599250 0.69912
NM_006514.4(SCN10A):c.3507+249C>G rs7617547 0.46953
NM_006514.4(SCN10A):c.*123C>T rs6599240 0.44172
NM_006514.4(SCN10A):c.3508-189G>T rs6805187 0.42313
NM_006514.4(SCN10A):c.599+62G>A rs4420804 0.42127
NM_006514.4(SCN10A):c.884-13T>C rs7641844 0.30982
NM_006514.4(SCN10A):c.3805-240A>G rs62242430 0.25302
NM_006514.4(SCN10A):c.2280+35C>T rs9830687 0.25291
NM_006514.4(SCN10A):c.599+120C>T rs10212338 0.25242
NM_006514.4(SCN10A):c.3805-41G>A rs6781740 0.25086
NM_006514.4(SCN10A):c.471-111A>G rs62244081 0.22654
NM_006514.4(SCN10A):c.3682-329T>C rs61014925 0.21303
NM_006514.4(SCN10A):c.4323A>G (p.Lys1441=) rs6790627 0.20722
NM_006514.4(SCN10A):c.1476C>T (p.Leu492=) rs7617919 0.20158
NM_006514.4(SCN10A):c.1461+294T>C rs12630795 0.20098
NM_006514.4(SCN10A):c.1284G>A (p.Glu428=) rs62244070 0.20052
NM_006514.4(SCN10A):c.2640+165G>A rs34786326 0.19932
NM_006514.4(SCN10A):c.1462-265A>G rs7431144 0.17025
NM_006514.4(SCN10A):c.270+148C>A rs11719241 0.11599
NM_006514.4(SCN10A):c.600-43G>C rs73826327 0.09441
NM_006514.4(SCN10A):c.2280+298C>T rs72866253 0.09094
NM_006514.4(SCN10A):c.1868-118A>C rs72866265 0.09091
NM_006514.4(SCN10A):c.1525T>C (p.Ser509Pro) rs7630989 0.08988
NM_006514.4(SCN10A):c.1867+82G>A rs12494065 0.08873
NM_006514.4(SCN10A):c.1868-36T>G rs7618620 0.08643
NM_006514.4(SCN10A):c.1755+251A>T rs7373595 0.08056
NM_006514.4(SCN10A):c.3682-206A>T rs6796459 0.07601
NM_006514.4(SCN10A):c.3682-66T>C rs6793226 0.07600
NM_006514.4(SCN10A):c.2641-95C>G rs73825883 0.06788
NM_006514.4(SCN10A):c.1290+237G>A rs7374030 0.06685
NM_006514.4(SCN10A):c.2280+263T>C rs73826310 0.05716
NM_006514.4(SCN10A):c.1867+57G>A rs12054245 0.05614
NM_006514.4(SCN10A):c.4282-165G>A rs78376096 0.04453
NM_006514.4(SCN10A):c.270+133A>T rs79414348 0.04285
NM_006514.4(SCN10A):c.3805-156C>T rs7372672 0.04099
NM_006514.4(SCN10A):c.1868-208A>C rs72866266 0.03125
NM_006514.4(SCN10A):c.2640+170G>T rs75284873 0.02979
NM_006514.4(SCN10A):c.470+63G>A rs75062405 0.02369
NM_006514.4(SCN10A):c.5217C>T (p.Asp1739=) rs116353929 0.02232
NM_006514.4(SCN10A):c.390-265A>C rs116529743 0.02041
NM_006514.4(SCN10A):c.4710G>A (p.Thr1570=) rs78425180 0.01966
NM_006514.4(SCN10A):c.4090-19C>T rs77494117 0.01447
NM_006514.4(SCN10A):c.618A>G (p.Ile206Met) rs74717885 0.01345
NM_006514.4(SCN10A):c.5089G>A (p.Val1697Ile) rs77804526 0.00850
NM_006514.4(SCN10A):c.45C>T (p.Arg15=) rs34314583 0.00684
NM_006514.4(SCN10A):c.4009T>A (p.Ser1337Thr) rs11711062 0.00451
NM_006514.4(SCN10A):c.4657+16C>T rs115824540 0.00446
NM_006514.4(SCN10A):c.4656G>A (p.Ala1552=) rs151182542 0.00431
NM_006514.4(SCN10A):c.1768G>A (p.Gly590Arg) rs35332705 0.00371
NM_006514.4(SCN10A):c.5657C>T (p.Ala1886Val) rs142653846 0.00318
NM_006514.4(SCN10A):c.268C>T (p.Arg90Trp) rs144270136 0.00148
NM_006514.4(SCN10A):c.4984G>A (p.Gly1662Ser) rs151090729 0.00047
NM_006514.4(SCN10A):c.3542C>T (p.Thr1181Met) rs150773437 0.00026
NM_006514.4(SCN10A):c.5047C>T (p.Pro1683Ser) rs146999807 0.00025
NM_006514.4(SCN10A):c.4379G>A (p.Arg1460Gln) rs369399424 0.00001
NM_006514.4(SCN10A):c.4680T>G (p.Leu1560=) rs529845623 0.00001
NM_006514.4(SCN10A):c.2106+44C>T rs72866260
NM_006514.4(SCN10A):c.4658-244C>T rs62243861
NM_006514.4(SCN10A):c.5605C>T (p.Arg1869Cys) rs141648641

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