ClinVar Miner

List of variants in gene SCN10A reported as benign for not specified

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Total variants: 24
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HGVS dbSNP
NM_006514.3(SCN10A):c.1284G>A (p.Glu428=) rs62244070
NM_006514.3(SCN10A):c.1453C>T (p.Arg485Cys) rs151153639
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.1868-9A>G rs6599250
NM_006514.3(SCN10A):c.3542C>T (p.Thr1181Met) rs150773437
NM_006514.3(SCN10A):c.4009T>A (p.Ser1337Thr) rs11711062
NM_006514.3(SCN10A):c.4090-19C>T rs77494117
NM_006514.3(SCN10A):c.4323A>G (p.Lys1441=) rs6790627
NM_006514.3(SCN10A):c.45C>T (p.Arg15=) rs34314583
NM_006514.3(SCN10A):c.4656G>A (p.Ala1552=) rs151182542
NM_006514.3(SCN10A):c.4657+16C>T rs115824540
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.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.5657C>T (p.Ala1886Val) rs142653846
NM_006514.3(SCN10A):c.618A>G (p.Ile206Met) rs74717885
NM_006514.3(SCN10A):c.884-13T>C rs7641844

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