ClinVar Miner

List of variants in gene SCN5A reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_000335.5(SCN5A):c.1890+50C>T rs9827213 0.00996
NM_000335.5(SCN5A):c.4215G>A (p.Gly1405=) rs41311123 0.00859
NM_000335.5(SCN5A):c.1967C>T (p.Pro656Leu) rs41313681 0.00115
NM_000335.5(SCN5A):c.6013C>G (p.Pro2005Ala) rs45489199 0.00109
NM_000335.5(SCN5A):c.856G>T (p.Ala286Ser) rs61746118 0.00089
NM_000335.5(SCN5A):c.5793G>A (p.Ala1931=) rs200594132 0.00070
NM_000335.5(SCN5A):c.5504T>C (p.Ile1835Thr) rs45563942 0.00066
NM_000335.5(SCN5A):c.895T>A (p.Leu299Met) rs199473087 0.00053
NM_000335.5(SCN5A):c.3663+10T>C rs200656652 0.00046
NM_000335.5(SCN5A):c.1479G>A (p.Arg493=) rs138870926 0.00043
NM_000335.5(SCN5A):c.456C>T (p.Asp152=) rs190803993 0.00031
NM_000335.5(SCN5A):c.4932G>A (p.Thr1644=) rs376150162 0.00030
NM_000335.5(SCN5A):c.4785C>T (p.Phe1595=) rs141789366 0.00027
NM_000335.5(SCN5A):c.4200C>T (p.Asn1400=) rs778436757 0.00013
NM_000335.5(SCN5A):c.4779C>T (p.Phe1593=) rs376720757 0.00013
NM_000335.5(SCN5A):c.5130C>T (p.Ala1710=) rs377478501 0.00011
NM_000335.5(SCN5A):c.5199C>T (p.Asn1733=) rs368980118 0.00010
NM_000335.5(SCN5A):c.5397A>G (p.Lys1799=) rs140641458 0.00010
NM_000335.5(SCN5A):c.5556T>C (p.Ile1852=) rs188792047 0.00010
NM_000335.5(SCN5A):c.2103G>A (p.Pro701=) rs564847999 0.00009
NM_000335.5(SCN5A):c.3951G>A (p.Glu1317=) rs769473892 0.00009
NM_000335.5(SCN5A):c.885G>A (p.Glu295=) rs373342830 0.00009
NM_000335.5(SCN5A):c.435C>T (p.Cys145=) rs587781159 0.00004
NM_000335.5(SCN5A):c.4435-10C>T rs747594441 0.00004
NM_000335.5(SCN5A):c.5172G>A (p.Pro1724=) rs372629753 0.00004
NM_000335.5(SCN5A):c.1188C>T (p.Val396=) rs749683415 0.00003
NM_000335.5(SCN5A):c.1557T>C (p.Ser519=) rs371560571 0.00003
NM_000335.5(SCN5A):c.3831C>T (p.Ile1277=) rs778600514 0.00003
NM_000335.5(SCN5A):c.5415T>A (p.Thr1805=) rs777429289 0.00003
NM_000335.5(SCN5A):c.480C>T (p.Val160=) rs549015769 0.00002
NM_000335.5(SCN5A):c.5673C>T (p.Ile1891=) rs763463291 0.00001
NM_000335.5(SCN5A):c.6000C>T (p.Leu2000=) rs538707712 0.00001
NM_000335.5(SCN5A):c.3468C>T (p.Leu1156=) rs570719978
NM_000335.5(SCN5A):c.393-4G>C
NM_000335.5(SCN5A):c.4422A>G (p.Gln1474=) rs2125835217
NM_000335.5(SCN5A):c.5848G>T (p.Val1950Leu) rs41315493
NM_000335.5(SCN5A):c.6003C>A (p.Ala2001=)

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