ClinVar Miner

List of variants in gene SCN5A reported by Integrated Genetics/Laboratory Corporation of America

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 66
Download table as spreadsheet
HGVS dbSNP
NM_000335.4(SCN5A):c.1065C>T (p.Phe355=) rs45570333
NM_000335.4(SCN5A):c.1066G>A (p.Asp356Asn) rs199473565
NM_000335.4(SCN5A):c.1152C>T (p.Ser384=) rs372970828
NM_000335.4(SCN5A):c.1236C>T (p.Val412=) rs45565936
NM_000335.4(SCN5A):c.1338+3G>A rs1553704675
NM_000335.4(SCN5A):c.1535C>T (p.Thr512Ile) rs199473118
NM_000335.4(SCN5A):c.1579G>A (p.Gly527Arg) rs763550164
NM_000335.4(SCN5A):c.1587T>C (p.Ile529=) rs45624133
NM_000335.4(SCN5A):c.1681C>T (p.Leu561=) rs45522138
NM_000335.4(SCN5A):c.1715C>A (p.Ala572Asp) rs36210423
NM_000335.4(SCN5A):c.1734C>T (p.Pro578=) rs200868190
NM_000335.4(SCN5A):c.1735G>A (p.Gly579Arg) rs199473128
NM_000335.4(SCN5A):c.1752C>G (p.Gly584=) rs1166588443
NM_000335.4(SCN5A):c.1813G>A (p.Gly605Arg) rs1553704001
NM_000335.4(SCN5A):c.1844G>A (p.Gly615Glu) rs12720452
NM_000335.4(SCN5A):c.1852C>T (p.Leu618Phe) rs45488304
NM_000335.4(SCN5A):c.1891-8G>A rs12720064
NM_000335.4(SCN5A):c.1943C>T (p.Pro648Leu) rs45609733
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.2182G>A (p.Val728Ile) rs958480279
NM_000335.4(SCN5A):c.2364C>T (p.Ile788=) rs183177363
NM_000335.4(SCN5A):c.2399G>A (p.Arg800His) rs566251672
NM_000335.4(SCN5A):c.2431C>T (p.Arg811Cys) rs794728864
NM_000335.4(SCN5A):c.2436+12G>A rs41312419
NM_000335.4(SCN5A):c.2437-5C>A rs72549411
NM_000335.4(SCN5A):c.2440C>T (p.Arg814Trp) rs199473161
NM_000335.4(SCN5A):c.2496C>T (p.Ile832=) rs761287478
NM_000335.4(SCN5A):c.2575C>T (p.Gln859Ter) rs794728865
NM_000335.4(SCN5A):c.2770G>A (p.Val924Ile) rs199473177
NM_000335.4(SCN5A):c.3389C>T (p.Thr1130Ile) rs199473197
NM_000335.4(SCN5A):c.3503C>T (p.Thr1168Ile) rs779305181
NM_000335.4(SCN5A):c.3508+10C>T rs41258454
NM_000335.4(SCN5A):c.3509-1G>C rs1553698563
NM_000335.4(SCN5A):c.3681C>G (p.Tyr1227Ter) rs1559738598
NM_000335.4(SCN5A):c.3875T>C (p.Phe1292Ser) rs41311127
NM_000335.4(SCN5A):c.3943C>T (p.Arg1315Ter) rs1553695764
NM_000335.4(SCN5A):c.3951G>A (p.Glu1317=) rs769473892
NM_000335.4(SCN5A):c.3985G>A (p.Ala1329Thr) rs199473224
NM_000335.4(SCN5A):c.4098A>G (p.Thr1366=) rs563832893
NM_000335.4(SCN5A):c.4215G>A (p.Gly1405=) rs41311123
NM_000335.4(SCN5A):c.4434+13C>T rs148598985
NM_000335.4(SCN5A):c.4506C>T (p.Ser1502=) rs45548237
NM_000335.4(SCN5A):c.5034C>T (p.Phe1678=) rs867169736
NM_000335.4(SCN5A):c.5181C>T (p.Cys1727=) rs193922726
NM_000335.4(SCN5A):c.5199C>T (p.Asn1733=) rs368980118
NM_000335.4(SCN5A):c.5256C>T (p.Thr1752=) rs1553692850
NM_000335.4(SCN5A):c.5317A>T (p.Asn1773Tyr) rs199473633
NM_000335.4(SCN5A):c.5347G>A (p.Glu1783Lys) rs137854601
NM_000335.4(SCN5A):c.5421T>A (p.Phe1807Leu) rs1553692688
NM_000335.4(SCN5A):c.5454_5455inv (p.Ala1819Thr)
NM_000335.4(SCN5A):c.5536C>T (p.Arg1846Cys) rs768246863
NM_000335.4(SCN5A):c.5709G>A (p.Ser1903=) rs376826051
NM_000335.4(SCN5A):c.5730C>T (p.Ala1910=) rs781163189
NM_000335.4(SCN5A):c.5848G>T (p.Val1950Leu) rs41315493
NM_000335.4(SCN5A):c.5901C>G (p.Ile1967Met) rs199473333
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.610G>A (p.Ala204Thr) rs1378168869
NM_000335.4(SCN5A):c.630G>A (p.Val210=) rs193922727
NM_000335.4(SCN5A):c.647C>T (p.Ser216Leu) rs41276525
NM_000335.4(SCN5A):c.659C>T (p.Thr220Ile) rs45620037
NM_000335.4(SCN5A):c.689T>C (p.Ile230Thr) rs199473073
NM_000335.4(SCN5A):c.717C>T (p.Ile239=) rs41285129
NM_000335.4(SCN5A):c.844C>T (p.Arg282Cys) rs199473082
NM_000335.4(SCN5A):c.856G>T (p.Ala286Ser) rs61746118

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.