ClinVar Miner

List of variants in gene SCN10A reported as benign for Brugada syndrome

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_006514.3(SCN10A):c.1157T>G (p.Phe386Cys) rs78555408
NM_006514.3(SCN10A):c.1453C>T (p.Arg485Cys) rs151153639
NM_006514.3(SCN10A):c.1768G>A (p.Gly590Arg) rs35332705
NM_006514.3(SCN10A):c.268C>T (p.Arg90Trp) rs144270136
NM_006514.3(SCN10A):c.3542C>T (p.Thr1181Met) rs150773437
NM_006514.3(SCN10A):c.390-9G>A rs370917734
NM_006514.3(SCN10A):c.4009T>A (p.Ser1337Thr) rs11711062
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.4656G>A (p.Ala1552=) rs151182542
NM_006514.3(SCN10A):c.4694G>A (p.Ser1565Asn) rs200063383
NM_006514.3(SCN10A):c.4710G>A (p.Thr1570=) rs78425180
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.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.5657C>T (p.Ala1886Val) rs142653846
NM_006514.3(SCN10A):c.5834A>G (p.Glu1945Gly) rs372702302
NM_006514.3(SCN10A):c.618A>G (p.Ile206Met) rs74717885
NM_006514.3(SCN10A):c.648A>C (p.Thr216=) rs150977149

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