ClinVar Miner

List of variants in gene SCN5A reported as likely benign for Cardiovascular phenotype

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Total variants: 70
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HGVS dbSNP
NM_000335.4(SCN5A):c.1008G>A (p.Pro336=) rs200285003
NM_000335.4(SCN5A):c.102C>T (p.Arg34=) rs41313239
NM_000335.4(SCN5A):c.1044C>T (p.Pro348=) rs370346797
NM_000335.4(SCN5A):c.1065C>T (p.Phe355=) rs45570333
NM_000335.4(SCN5A):c.1188C>T (p.Val396=) rs749683415
NM_000335.4(SCN5A):c.1236C>T (p.Val412=) rs45565936
NM_000335.4(SCN5A):c.1272C>T (p.Ile424=) rs267599794
NM_000335.4(SCN5A):c.1335C>T (p.His445=) rs368045716
NM_000335.4(SCN5A):c.1681C>T (p.Leu561=) rs45522138
NM_000335.4(SCN5A):c.1714_1715delinsTT (p.Ala572Phe) rs730880211
NM_000335.4(SCN5A):c.1755C>T (p.His585=) rs201024847
NM_000335.4(SCN5A):c.1852C>T (p.Leu618Phe) rs45488304
NM_000335.4(SCN5A):c.1902G>A (p.Ser634=) rs764360705
NM_000335.4(SCN5A):c.2001C>T (p.Ser667=) rs587781161
NM_000335.4(SCN5A):c.2013C>T (p.Ser671=) rs751050999
NM_000335.4(SCN5A):c.2074C>A (p.Gln692Lys) rs45553235
NM_000335.4(SCN5A):c.2103G>A (p.Pro701=) rs564847999
NM_000335.4(SCN5A):c.2181C>T (p.Ile727=) rs186942072
NM_000335.4(SCN5A):c.2184A>T (p.Val728=) rs886039142
NM_000335.4(SCN5A):c.2259C>T (p.Asn753=) rs878911306
NM_000335.4(SCN5A):c.2313C>T (p.Leu771=) rs876657580
NM_000335.4(SCN5A):c.2437-5C>A rs72549411
NM_000335.4(SCN5A):c.2484C>T (p.Leu828=) rs923903065
NM_000335.4(SCN5A):c.2529A>G (p.Thr843=) rs771936542
NM_000335.4(SCN5A):c.3495C>T (p.Asp1165=) rs1358339064
NM_000335.4(SCN5A):c.357C>G (p.Pro119=) rs749556647
NM_000335.4(SCN5A):c.3618C>T (p.Phe1206=) rs184934308
NM_000335.4(SCN5A):c.3627C>T (p.Phe1209=) rs962909965
NM_000335.4(SCN5A):c.3645A>T (p.Leu1215=) rs760539539
NM_000335.4(SCN5A):c.3723C>T (p.Ala1241=) rs61737829
NM_000335.4(SCN5A):c.3870G>A (p.Leu1290=) rs41313033
NM_000335.4(SCN5A):c.3909G>A (p.Thr1303=) rs764462471
NM_000335.4(SCN5A):c.3910C>T (p.Leu1304=) rs1553695779
NM_000335.4(SCN5A):c.4068G>A (p.Ala1356=) rs187370816
NM_000335.4(SCN5A):c.4167C>T (p.Thr1389=) rs747356664
NM_000335.4(SCN5A):c.4209C>T (p.Asn1403=) rs397517954
NM_000335.4(SCN5A):c.4299T>C (p.Tyr1433=) rs200556220
NM_000335.4(SCN5A):c.4401C>T (p.Val1467=) rs766197312
NM_000335.4(SCN5A):c.4506C>T (p.Ser1502=) rs45548237
NM_000335.4(SCN5A):c.456C>T (p.Asp152=) rs190803993
NM_000335.4(SCN5A):c.4590C>T (p.Asp1530=) rs372507927
NM_000335.4(SCN5A):c.4626G>A (p.Val1542=) rs1444726385
NM_000335.4(SCN5A):c.486C>T (p.Tyr162=) rs45489099
NM_000335.4(SCN5A):c.4932G>A (p.Thr1644=) rs376150162
NM_000335.4(SCN5A):c.5169G>A (p.Gly1723=) rs1553692900
NM_000335.4(SCN5A):c.5199C>T (p.Asn1733=) rs368980118
NM_000335.4(SCN5A):c.5357G>A (p.Ser1786Asn) rs199473316
NM_000335.4(SCN5A):c.5364C>T (p.Asp1788=) rs375752426
NM_000335.4(SCN5A):c.5424T>C (p.Ile1808=) rs769534824
NM_000335.4(SCN5A):c.5451C>T (p.Ala1817=) rs370114378
NM_000335.4(SCN5A):c.5709G>A (p.Ser1903=) rs376826051
NM_000335.4(SCN5A):c.5718T>C (p.Val1906=) rs1553692515
NM_000335.4(SCN5A):c.5793G>A (p.Ala1931=) rs200594132
NM_000335.4(SCN5A):c.5793G>C (p.Ala1931=) rs200594132
NM_000335.4(SCN5A):c.5799C>T (p.Ser1933=) rs375254452
NM_000335.4(SCN5A):c.5882C>T (p.Pro1961Leu) rs199473638
NM_000335.4(SCN5A):c.5886C>T (p.Pro1962=) rs889590315
NM_000335.4(SCN5A):c.6000C>T (p.Leu2000=) rs538707712
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.630G>A (p.Val210=) rs193922727
NM_000335.4(SCN5A):c.681G>A (p.Leu227=) rs369623575
NM_000335.4(SCN5A):c.717C>T (p.Ile239=) rs41285129
NM_000335.4(SCN5A):c.726C>A (p.Ala242=) rs746812420
NM_000335.4(SCN5A):c.744G>A (p.Lys248=) rs45453395
NM_000335.4(SCN5A):c.801C>T (p.Ile267=) rs45587735
NM_000335.4(SCN5A):c.856G>T (p.Ala286Ser) rs61746118
NM_000335.4(SCN5A):c.864C>T (p.Asn288=) rs373728726
NM_000335.4(SCN5A):c.895T>A (p.Leu299Met) rs199473087
NM_000335.4(SCN5A):c.990T>G (p.Ser330=) rs779310644

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