ClinVar Miner

List of variants in gene SCN10A reported as uncertain significance for Brugada syndrome

Included ClinVar conditions (23):
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Gene type:
ClinVar version:
Total variants: 121
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HGVS dbSNP
NM_006514.3(SCN10A):c.1052G>A (p.Arg351His)
NM_006514.3(SCN10A):c.1093-3C>A rs373289770
NM_006514.3(SCN10A):c.1138G>C (p.Val380Leu) rs142276689
NM_006514.3(SCN10A):c.120G>T (p.Lys40Asn) rs1553626242
NM_006514.3(SCN10A):c.1276C>T (p.Arg426Trp)
NM_006514.3(SCN10A):c.1325T>G (p.Leu442Arg) rs1373914068
NM_006514.3(SCN10A):c.1370A>G (p.Glu457Gly) rs766017851
NM_006514.3(SCN10A):c.1430C>T (p.Pro477Leu) rs142235256
NM_006514.3(SCN10A):c.1454G>A (p.Arg485His) rs746690639
NM_006514.3(SCN10A):c.1486A>G (p.Lys496Glu) rs755100226
NM_006514.3(SCN10A):c.1489C>T (p.Arg497Cys)
NM_006514.3(SCN10A):c.149A>C (p.Lys50Thr)
NM_006514.3(SCN10A):c.1534C>G (p.Arg512Gly) rs200714519
NM_006514.3(SCN10A):c.1600C>T (p.Arg534Trp) rs542554745
NM_006514.3(SCN10A):c.1668A>T (p.Gln556His)
NM_006514.3(SCN10A):c.1715C>T (p.Pro572Leu) rs553784643
NM_006514.3(SCN10A):c.1730T>A (p.Leu577His) rs1060501716
NM_006514.3(SCN10A):c.1733C>T (p.Ala578Val)
NM_006514.3(SCN10A):c.1762G>A (p.Asp588Asn) rs747486328
NM_006514.3(SCN10A):c.1788G>T (p.Leu596Phe) rs764965507
NM_006514.3(SCN10A):c.1819G>A (p.Ala607Thr)
NM_006514.3(SCN10A):c.1824A>G (p.Gln608=)
NM_006514.3(SCN10A):c.1858G>A (p.Val620Ile) rs151303346
NM_006514.3(SCN10A):c.1945C>T (p.Pro649Ser) rs747848559
NM_006514.3(SCN10A):c.2052G>A (p.Met684Ile) rs1553619005
NM_006514.3(SCN10A):c.2158G>A (p.Asp720Asn) rs781354273
NM_006514.3(SCN10A):c.2202C>G (p.Cys734Trp) rs910678839
NM_006514.3(SCN10A):c.2222T>G (p.Leu741Arg) rs201342036
NM_006514.3(SCN10A):c.2266C>T (p.Arg756Trp) rs374341474
NM_006514.3(SCN10A):c.2275C>G (p.Arg759Gly)
NM_006514.3(SCN10A):c.2285G>A (p.Arg762His)
NM_006514.3(SCN10A):c.2312C>T (p.Pro771Leu) rs758157003
NM_006514.3(SCN10A):c.2341G>A (p.Gly781Arg)
NM_006514.3(SCN10A):c.2414G>T (p.Gly805Val)
NM_006514.3(SCN10A):c.2428G>T (p.Gly810Trp) rs145712124
NM_006514.3(SCN10A):c.243T>A (p.Asp81Glu) rs1060501717
NM_006514.3(SCN10A):c.2441G>A (p.Arg814His) rs139861061
NM_006514.3(SCN10A):c.2465C>T (p.Ala822Val) rs747839312
NM_006514.3(SCN10A):c.2476G>A (p.Asp826Asn) rs199535863
NM_006514.3(SCN10A):c.2476G>T (p.Asp826Tyr) rs199535863
NM_006514.3(SCN10A):c.2486G>A (p.Arg829His) rs752623537
NM_006514.3(SCN10A):c.257A>G (p.Tyr86Cys)
NM_006514.3(SCN10A):c.25G>A (p.Glu9Lys) rs747174454
NM_006514.3(SCN10A):c.263C>T (p.Thr88Ile) rs1226072923
NM_006514.3(SCN10A):c.2767C>T (p.Arg923Cys)
NM_006514.3(SCN10A):c.307C>T (p.Arg103Trp) rs750073618
NM_006514.3(SCN10A):c.319A>T (p.Thr107Ser)
NM_006514.3(SCN10A):c.3521A>G (p.Tyr1174Cys)
NM_006514.3(SCN10A):c.3550G>C (p.Ala1184Pro) rs759842238
NM_006514.3(SCN10A):c.3556C>A (p.Leu1186Met) rs192493052
NM_006514.3(SCN10A):c.3655delT (p.Cys1219Alafs)
NM_006514.3(SCN10A):c.365C>T (p.Thr122Met) rs142884499
NM_006514.3(SCN10A):c.3667T>C (p.Phe1223Leu) rs1334180362
NM_006514.3(SCN10A):c.3674T>C (p.Ile1225Thr) rs139638446
NM_006514.3(SCN10A):c.3675T>G (p.Ile1225Met) rs371834340
NM_006514.3(SCN10A):c.3691A>T (p.Ile1231Leu)
NM_006514.3(SCN10A):c.3749G>A (p.Arg1250Gln) rs774893568
NM_006514.3(SCN10A):c.3766C>T (p.Arg1256Trp) rs747044382
NM_006514.3(SCN10A):c.376G>A (p.Val126Met) rs1553625946
NM_006514.3(SCN10A):c.3778G>T (p.Ala1260Ser) rs779316495
NM_006514.3(SCN10A):c.3943G>A (p.Asp1315Asn)
NM_006514.3(SCN10A):c.3971C>T (p.Ser1324Leu)
NM_006514.3(SCN10A):c.3988T>A (p.Ser1330Thr)
NM_006514.3(SCN10A):c.3991G>A (p.Asp1331Asn)
NM_006514.3(SCN10A):c.4089+2T>C rs1553614805
NM_006514.3(SCN10A):c.4094C>A (p.Thr1365Asn) rs748854017
NM_006514.3(SCN10A):c.40C>T (p.Arg14Cys)
NM_006514.3(SCN10A):c.410C>T (p.Thr137Met) rs148663098
NM_006514.3(SCN10A):c.4139G>A (p.Arg1380Gln) rs149155352
NM_006514.3(SCN10A):c.4150A>G (p.Met1384Val)
NM_006514.3(SCN10A):c.4164G>A (p.Trp1388Ter) rs756253735
NM_006514.3(SCN10A):c.4174G>A (p.Val1392Met) rs539215014
NM_006514.3(SCN10A):c.4208T>C (p.Ile1403Thr) rs140825889
NM_006514.3(SCN10A):c.4221C>A (p.Phe1407Leu) rs1060501715
NM_006514.3(SCN10A):c.4266T>A (p.Asn1422Lys)
NM_006514.3(SCN10A):c.4327T>C (p.Tyr1443His) rs762798134
NM_006514.3(SCN10A):c.4396C>T (p.Gln1466Ter) rs199931920
NM_006514.3(SCN10A):c.4421C>A (p.Thr1474Asn)
NM_006514.3(SCN10A):c.4468A>G (p.Met1490Val)
NM_006514.3(SCN10A):c.4514C>T (p.Thr1505Met)
NM_006514.3(SCN10A):c.4552G>A (p.Val1518Ile) rs202040659
NM_006514.3(SCN10A):c.4585G>A (p.Ala1529Thr) rs757916036
NM_006514.3(SCN10A):c.4639G>T (p.Val1547Leu) rs377492327
NM_006514.3(SCN10A):c.4655C>T (p.Ala1552Val) rs756133876
NM_006514.3(SCN10A):c.4663A>T (p.Ile1555Phe) rs754130748
NM_006514.3(SCN10A):c.4672G>A (p.Ala1558Thr)
NM_006514.3(SCN10A):c.4709C>T (p.Thr1570Met) rs772484960
NM_006514.3(SCN10A):c.472T>G (p.Tyr158Asp) rs202192818
NM_006514.3(SCN10A):c.4744C>T (p.Arg1582Cys) rs569261408
NM_006514.3(SCN10A):c.4777A>T (p.Ile1593Phe) rs762600386
NM_006514.3(SCN10A):c.4849G>T (p.Val1617Phe) rs375940680
NM_006514.3(SCN10A):c.4873_4878delGGTATGinsATCTACTCCA (p.Gly1625Ilefs) rs1553613078
NM_006514.3(SCN10A):c.4878G>A (p.Met1626Ile) rs371337228
NM_006514.3(SCN10A):c.5140G>A (p.Val1714Ile) rs1553612991
NM_006514.3(SCN10A):c.5144A>C (p.Asn1715Thr) rs777258179
NM_006514.3(SCN10A):c.5144A>G (p.Asn1715Ser) rs777258179
NM_006514.3(SCN10A):c.5200G>A (p.Glu1734Lys) rs200645452
NM_006514.3(SCN10A):c.5249A>G (p.Lys1750Arg)
NM_006514.3(SCN10A):c.5256C>A (p.Asp1752Glu)
NM_006514.3(SCN10A):c.5294C>T (p.Ser1765Leu)
NM_006514.3(SCN10A):c.5342A>G (p.Asn1781Ser) rs372368062
NM_006514.3(SCN10A):c.5371C>A (p.Pro1791Thr) rs371803816
NM_006514.3(SCN10A):c.542A>C (p.Glu181Ala) rs142203439
NM_006514.3(SCN10A):c.544T>A (p.Phe182Ile) rs1553623225
NM_006514.3(SCN10A):c.5540G>A (p.Arg1847Gln) rs148537653
NM_006514.3(SCN10A):c.5548C>T (p.Gln1850Ter) rs149504103
NM_006514.3(SCN10A):c.5694delA (p.Ala1899Glnfs)
NM_006514.3(SCN10A):c.5698A>G (p.Asn1900Asp) rs1265687114
NM_006514.3(SCN10A):c.5705A>C (p.Asn1902Thr) rs756547221
NM_006514.3(SCN10A):c.5866C>A (p.Pro1956Thr) rs748441157
NM_006514.3(SCN10A):c.599C>T (p.Ala200Val)
NM_006514.3(SCN10A):c.61C>G (p.Leu21Val) rs1553626259
NM_006514.3(SCN10A):c.682G>A (p.Val228Met) rs141368548
NM_006514.3(SCN10A):c.688C>G (p.Pro230Ala) rs147844607
NM_006514.3(SCN10A):c.724T>A (p.Ser242Thr) rs140288103
NM_006514.3(SCN10A):c.753C>G (p.Ile251Met) rs747296872
NM_006514.3(SCN10A):c.760A>T (p.Ile254Phe) rs766143752
NM_006514.3(SCN10A):c.883C>T (p.Pro295Ser) rs371909817
NM_006514.3(SCN10A):c.890T>C (p.Ile297Thr)
NM_006514.3(SCN10A):c.905G>A (p.Arg302Gln) rs201955990
NM_006514.3(SCN10A):c.955T>A (p.Cys319Ser) rs199715855

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