ClinVar Miner

List of variants in gene SCN5A studied for Brugada syndrome 1; Long QT syndrome 3; Sick sinus syndrome 1, autosomal recessive; Progressive familial heart block type 1A; Paroxysmal familial ventricular fibrillation 1; Dilated cardiomyopathy 1E; SUDDEN INFANT DEATH SYNDROME; Atrial fibrillation, familial, 10

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Total variants: 15
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HGVS dbSNP
NM_000335.4(SCN5A):c.1099C>T (p.Arg367Cys) rs199473097
NM_000335.4(SCN5A):c.1282G>A (p.Glu428Lys) rs199473111
NM_000335.4(SCN5A):c.152C>T (p.Ala51Val) rs727505131
NM_000335.4(SCN5A):c.2399G>A (p.Arg800His) rs566251672
NM_000335.4(SCN5A):c.3553G>A (p.Ala1185Thr) rs199473595
NM_000335.4(SCN5A):c.4783T>A (p.Phe1595Ile) rs199473278
NM_000335.4(SCN5A):c.5686C>T (p.Arg1896Trp) rs45465995
NM_000335.4(SCN5A):c.5735G>A (p.Arg1912His) rs199473327
NM_000335.4(SCN5A):c.5783G>A (p.Arg1928His) rs727504822
NM_000335.4(SCN5A):c.5792C>T (p.Ala1931Val)
NM_000335.4(SCN5A):c.5800G>A (p.Gly1934Ser) rs199473637
NM_000335.4(SCN5A):c.5869C>T (p.Arg1957Ter) rs757532106
NM_000335.4(SCN5A):c.5901C>G (p.Ile1967Met) rs199473333
NM_000335.4(SCN5A):c.665G>A (p.Arg222Gln) rs45546039
NM_000335.4(SCN5A):c.880G>A (p.Val294Met) rs199473086

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