ClinVar Miner

List of variants in gene SCN5A reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 96
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HGVS dbSNP
NM_000335.4(SCN5A):c.1008G>A (p.Pro336=) rs200285003
NM_000335.4(SCN5A):c.100C>T (p.Arg34Cys) rs6791924
NM_000335.4(SCN5A):c.1017C>T (p.Tyr339=) rs17215493
NM_000335.4(SCN5A):c.1044C>T (p.Pro348=) rs370346797
NM_000335.4(SCN5A):c.1050C>T (p.His350=) rs587781160
NM_000335.4(SCN5A):c.1065C>T (p.Phe355=) rs45570333
NM_000335.4(SCN5A):c.1068T>C (p.Asp356=) rs41313703
NM_000335.4(SCN5A):c.1141-3C>A rs41312433
NM_000335.4(SCN5A):c.1141-4C>T rs794728840
NM_000335.4(SCN5A):c.1152C>T (p.Ser384=) rs372970828
NM_000335.4(SCN5A):c.1195C>T (p.Leu399=) rs369253900
NM_000335.4(SCN5A):c.1236C>T (p.Val412=) rs45565936
NM_000335.4(SCN5A):c.1281C>T (p.Thr427=) rs375989197
NM_000335.4(SCN5A):c.1302C>T (p.Phe434=) rs41313699
NM_000335.4(SCN5A):c.1339-24G>A rs7428779
NM_000335.4(SCN5A):c.1381T>G (p.Leu461Val) rs41313697
NM_000335.4(SCN5A):c.1441C>T (p.Arg481Trp) rs144511230
NM_000335.4(SCN5A):c.1479G>A (p.Arg493=) rs138870926
NM_000335.4(SCN5A):c.1569T>A (p.Arg523=) rs41313693
NM_000335.4(SCN5A):c.1571C>A (p.Ser524Tyr) rs41313691
NM_000335.4(SCN5A):c.1587T>C (p.Ile529=) rs45624133
NM_000335.4(SCN5A):c.1673A>G (p.His558Arg) rs1805124
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.1743G>A (p.Ser581=) rs41313687
NM_000335.4(SCN5A):c.1755C>T (p.His585=) rs201024847
NM_000335.4(SCN5A):c.1821C>T (p.Gly607=) rs753835985
NM_000335.4(SCN5A):c.1842A>G (p.Pro614=) rs766696979
NM_000335.4(SCN5A):c.1852C>T (p.Leu618Phe) rs45488304
NM_000335.4(SCN5A):c.1890+14G>A rs145427253
NM_000335.4(SCN5A):c.1967C>T (p.Pro656Leu) rs41313681
NM_000335.4(SCN5A):c.2001C>T (p.Ser667=) rs587781161
NM_000335.4(SCN5A):c.2151G>A (p.Pro717=) rs191840835
NM_000335.4(SCN5A):c.21T>A (p.Pro7=) rs587781157
NM_000335.4(SCN5A):c.2253C>T (p.Val751=) rs371649934
NM_000335.4(SCN5A):c.2263-18T>C rs9835588
NM_000335.4(SCN5A):c.2436+12G>A rs41312419
NM_000335.4(SCN5A):c.2437-5C>A rs72549411
NM_000335.4(SCN5A):c.274-24C>T rs7627488
NM_000335.4(SCN5A):c.2787+13_2787+17del rs794728841
NM_000335.4(SCN5A):c.2787+17C>A rs587781163
NM_000335.4(SCN5A):c.3388-7T>C rs41310769
NM_000335.4(SCN5A):c.3508+10C>T rs41258454
NM_000335.4(SCN5A):c.3508+12G>A rs587781164
NM_000335.4(SCN5A):c.3537G>A (p.Ala1179=) rs370990219
NM_000335.4(SCN5A):c.354C>T (p.His118=) rs45533640
NM_000335.4(SCN5A):c.3575G>A (p.Arg1192Gln) rs41261344
NM_000335.4(SCN5A):c.360C>T (p.Ile120=) rs587781158
NM_000335.4(SCN5A):c.3618C>T (p.Phe1206=) rs184934308
NM_000335.4(SCN5A):c.3663+10T>C rs200656652
NM_000335.4(SCN5A):c.3664-7T>A rs373156650
NM_000335.4(SCN5A):c.3807C>T (p.Ala1269=) rs367927086
NM_000335.4(SCN5A):c.3870G>A (p.Leu1290=) rs41313033
NM_000335.4(SCN5A):c.3879C>T (p.Ala1293=) rs372132916
NM_000335.4(SCN5A):c.3909G>A (p.Thr1303=) rs764462471
NM_000335.4(SCN5A):c.3919C>T (p.Leu1307Phe) rs41313031
NM_000335.4(SCN5A):c.392+34C>A rs41312963
NM_000335.4(SCN5A):c.3951G>A (p.Glu1317=) rs769473892
NM_000335.4(SCN5A):c.4053C>T (p.Gly1351=) rs587781165
NM_000335.4(SCN5A):c.4083G>A (p.Arg1361=) rs377173580
NM_000335.4(SCN5A):c.4200C>T (p.Asn1400=) rs778436757
NM_000335.4(SCN5A):c.4215G>A (p.Gly1405=) rs41311123
NM_000335.4(SCN5A):c.4299T>C (p.Tyr1433=) rs200556220
NM_000335.4(SCN5A):c.42C>T (p.Arg14=) rs183988524
NM_000335.4(SCN5A):c.435C>T (p.Cys145=) rs587781159
NM_000335.4(SCN5A):c.4434+13C>T rs148598985
NM_000335.4(SCN5A):c.4467G>A (p.Glu1489=) rs375026424
NM_000335.4(SCN5A):c.4506C>T (p.Ser1502=) rs45548237
NM_000335.4(SCN5A):c.4785C>T (p.Phe1595=) rs141789366
NM_000335.4(SCN5A):c.4811-5C>T rs765962519
NM_000335.4(SCN5A):c.482+16G>C rs41312949
NM_000335.4(SCN5A):c.4821C>T (p.Leu1607=) rs45437099
NM_000335.4(SCN5A):c.4845C>T (p.Phe1615=) rs41315495
NM_000335.4(SCN5A):c.486C>T (p.Tyr162=) rs45489099
NM_000335.4(SCN5A):c.4887A>T (p.Ile1629=) rs201559770
NM_000335.4(SCN5A):c.4932G>A (p.Thr1644=) rs376150162
NM_000335.4(SCN5A):c.5061C>T (p.Ile1687=) rs145731678
NM_000335.4(SCN5A):c.5172G>A (p.Pro1724=) rs372629753
NM_000335.4(SCN5A):c.5199C>T (p.Asn1733=) rs368980118
NM_000335.4(SCN5A):c.52C>T (p.Arg18Trp) rs199473044
NM_000335.4(SCN5A):c.5301T>C (p.Ile1767=) rs587781166
NM_000335.4(SCN5A):c.5364C>T (p.Asp1788=) rs375752426
NM_000335.4(SCN5A):c.5451C>T (p.Ala1817=) rs370114378
NM_000335.4(SCN5A):c.5454T>C (p.Asp1818=) rs1805126
NM_000335.4(SCN5A):c.5604C>T (p.Asp1868=) rs560476223
NM_000335.4(SCN5A):c.5793G>A (p.Ala1931=) rs200594132
NM_000335.4(SCN5A):c.5799C>T (p.Ser1933=) rs375254452
NM_000335.4(SCN5A):c.5841C>T (p.Ile1947=) rs13324293
NM_000335.4(SCN5A):c.5848G>T (p.Val1950Leu) rs41315493
NM_000335.4(SCN5A):c.6003C>T (p.Ala2001=) rs749546972
NM_000335.4(SCN5A):c.630G>A (p.Val210=) rs193922727
NM_000335.4(SCN5A):c.717C>T (p.Ile239=) rs41285129
NM_000335.4(SCN5A):c.795C>T (p.Ala265=) rs527692731
NM_000335.4(SCN5A):c.87A>G (p.Ala29=) rs6599230
NM_000335.4(SCN5A):c.885G>A (p.Glu295=) rs373342830
NM_001099404.1(SCN5A):c.648G>A (p.Ser216=) rs45475402

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