ClinVar Miner

List of variants in gene SCN5A reported as uncertain significance by Center for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues

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Total variants: 16
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NM_000335.4(SCN5A):c.1045G>A (p.Asp349Asn) rs779687673
NM_000335.4(SCN5A):c.1298G>A (p.Arg433His) rs879035421
NM_000335.4(SCN5A):c.142G>A (p.Glu48Lys) rs199473048
NM_000335.4(SCN5A):c.1844G>A (p.Gly615Glu) rs12720452
NM_000335.4(SCN5A):c.1943C>T (p.Pro648Leu) rs45609733
NM_000335.4(SCN5A):c.2213A>C (p.His738Pro) rs1135401948
NM_000335.4(SCN5A):c.2643G>T (p.Met881Ile) rs1559756973
NM_000335.4(SCN5A):c.422T>A (p.Ile141Asn) rs772186966
NM_000335.4(SCN5A):c.4390T>C (p.Phe1464Leu) rs1559728884
NM_000335.4(SCN5A):c.4502G>A (p.Gly1501Asp) rs1230010586
NM_000335.4(SCN5A):c.6007T>C (p.Phe2003Leu) rs41311117
NM_000335.4(SCN5A):c.6013C>G (p.Pro2005Ala) rs45489199
NM_000335.4(SCN5A):c.6031C>T (p.Arg2011Cys) rs199473640
NM_000335.4(SCN5A):c.659C>T (p.Thr220Ile) rs45620037
NM_000335.4(SCN5A):c.880G>A (p.Val294Met) rs199473086

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