ClinVar Miner

List of variants in gene SCN5A reported as likely benign for not provided

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Total variants: 45
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HGVS dbSNP
NC_000003.12:g.38598642_38598644del
NM_000335.4(SCN5A):c.1372C>T (p.Arg458Cys) rs752130196
NM_000335.4(SCN5A):c.1519-225G>C
NM_000335.4(SCN5A):c.1715C>A (p.Ala572Asp) rs36210423
NM_000335.4(SCN5A):c.1752C>G (p.Gly584=) rs1166588443
NM_000335.4(SCN5A):c.1852C>T (p.Leu618Phe) rs45488304
NM_000335.4(SCN5A):c.1890+50C>T rs9827213
NM_000335.4(SCN5A):c.1967C>T (p.Pro656Leu) rs41313681
NM_000335.4(SCN5A):c.2014G>A (p.Ala672Thr) rs199473140
NM_000335.4(SCN5A):c.2103G>A (p.Pro701=) rs564847999
NM_000335.4(SCN5A):c.2436+136C>G
NM_000335.4(SCN5A):c.2437-133_2437-132insT
NM_000335.4(SCN5A):c.2616C>T (p.Asp872=)
NM_000335.4(SCN5A):c.2770G>A (p.Val924Ile) rs199473177
NM_000335.4(SCN5A):c.3388-274T>C
NM_000335.4(SCN5A):c.3508+11G>A
NM_000335.4(SCN5A):c.3837+302G>A
NM_000335.4(SCN5A):c.3838-298G>A
NM_000335.4(SCN5A):c.3875T>C (p.Phe1292Ser) rs41311127
NM_000335.4(SCN5A):c.402C>T (p.Asn134=)
NM_000335.4(SCN5A):c.4174T>C (p.Leu1392=)
NM_000335.4(SCN5A):c.4243-4C>T rs772447988
NM_000335.4(SCN5A):c.4401C>T (p.Val1467=) rs766197312
NM_000335.4(SCN5A):c.4539+278C>A
NM_000335.4(SCN5A):c.4811-79dup
NM_000335.4(SCN5A):c.4811-80C>A
NM_000335.4(SCN5A):c.4811-82_4811-81insCA
NM_000335.4(SCN5A):c.4854G>A (p.Pro1618=) rs368031564
NM_000335.4(SCN5A):c.4857G>A (p.Thr1619=) rs753174463
NM_000335.4(SCN5A):c.495C>T (p.Thr165=) rs62242804
NM_000335.4(SCN5A):c.5256C>T (p.Thr1752=) rs1553692850
NM_000335.4(SCN5A):c.5504T>C (p.Ile1835Thr) rs45563942
NM_000335.4(SCN5A):c.5848G>T (p.Val1950Leu) rs41315493
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.611+16G>A
NM_000335.4(SCN5A):c.611+174G>A
NM_000335.4(SCN5A):c.611+237G>A
NM_000335.4(SCN5A):c.659C>T (p.Thr220Ile) rs45620037
NM_000335.4(SCN5A):c.703+6A>G rs781104838
NM_000335.4(SCN5A):c.748C>T (p.Leu250=)
NM_000335.4(SCN5A):c.80G>A (p.Arg27His) rs199473045
NM_000335.4(SCN5A):c.935-241C>T
NM_000335.4(SCN5A):c.935-46C>G
NM_000335.4(SCN5A):c.998+107G>A

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