ClinVar Miner

List of variants in gene SCN5A reported as likely benign for Brugada syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
Download table as spreadsheet
HGVS dbSNP
NM_001099404.1(SCN5A):c.5844C>T (p.Ile1948=) rs13324293
NM_001099404.1(SCN5A):c.87A>G (p.Ala29=) rs6599230
NM_198056.2(SCN5A):c.*1165C>T rs41313017
NM_198056.2(SCN5A):c.*123A>G rs7429945
NM_198056.2(SCN5A):c.*1453dup rs397763929
NM_198056.2(SCN5A):c.*1537T>C rs41315485
NM_198056.2(SCN5A):c.*159C>T rs41313019
NM_198056.2(SCN5A):c.*2145_*2146insGAGAAGAGAGTAGGAAAAAGGAGGG rs45592631
NM_198056.2(SCN5A):c.*753C>T rs41310757
NM_198056.2(SCN5A):c.*962T>A rs4073797
NM_198056.2(SCN5A):c.*963C>T rs4073796
NM_198056.2(SCN5A):c.100C>T (p.Arg34Cys) rs6791924
NM_198056.2(SCN5A):c.1140+10T>C rs1553704871
NM_198056.2(SCN5A):c.1141-3C>A rs41312433
NM_198056.2(SCN5A):c.1302C>T (p.Phe434=) rs41313699
NM_198056.2(SCN5A):c.1338+7G>A rs1431210369
NM_198056.2(SCN5A):c.1372C>T (p.Arg458Cys) rs752130196
NM_198056.2(SCN5A):c.1464G>A (p.Glu488=) rs1553704447
NM_198056.2(SCN5A):c.1557T>C (p.Ser519=) rs371560571
NM_198056.2(SCN5A):c.1653G>C (p.Ala551=) rs397517952
NM_198056.2(SCN5A):c.1673A>G (p.His558Arg) rs1805124
NM_198056.2(SCN5A):c.1715C>A (p.Ala572Asp) rs36210423
NM_198056.2(SCN5A):c.1905G>A (p.Glu635=) rs779179765
NM_198056.2(SCN5A):c.192G>T (p.Leu64=) rs372406427
NM_198056.2(SCN5A):c.2023+10C>G rs1553703209
NM_198056.2(SCN5A):c.2074C>A (p.Gln692Lys) rs45553235
NM_198056.2(SCN5A):c.2205G>A (p.Ala735=) rs376259799
NM_198056.2(SCN5A):c.2328C>T (p.Tyr776=) rs1553701160
NM_198056.2(SCN5A):c.2415G>A (p.Ser805=) rs754312452
NM_198056.2(SCN5A):c.2530C>T (p.Leu844=) rs1477210447
NM_198056.2(SCN5A):c.327C>T (p.Asn109=) rs199473056
NM_198056.2(SCN5A):c.3578G>A (p.Arg1193Gln) rs41261344
NM_198056.2(SCN5A):c.3750C>T (p.Phe1250=) rs756102773
NM_198056.2(SCN5A):c.3756G>C (p.Leu1252=) rs1410342625
NM_198056.2(SCN5A):c.3878T>C (p.Phe1293Ser) rs41311127
NM_198056.2(SCN5A):c.3900G>A (p.Lys1300=) rs1331519547
NM_198056.2(SCN5A):c.3912G>A (p.Thr1304=) rs764462471
NM_198056.2(SCN5A):c.3915G>A (p.Leu1305=) rs1035272918
NM_198056.2(SCN5A):c.4143G>A (p.Lys1381=) rs1553695286
NM_198056.2(SCN5A):c.4422C>T (p.Asn1474=) rs923406803
NM_198056.2(SCN5A):c.4594G>A (p.Val1532Ile) rs199473618
NM_198056.2(SCN5A):c.4662T>G (p.Pro1554=) rs777765659
NM_198056.2(SCN5A):c.4695G>A (p.Leu1565=) rs200284038
NM_198056.2(SCN5A):c.4698C>T (p.Leu1566=) rs727505094
NM_198056.2(SCN5A):c.4848C>T (p.Phe1616=) rs41315495
NM_198056.2(SCN5A):c.4980C>T (p.Ile1660=) rs752079563
NM_198056.2(SCN5A):c.5349C>T (p.Thr1783=) rs868549221
NM_198056.2(SCN5A):c.5457T>C (p.Asp1819=) rs1805126
NM_198056.2(SCN5A):c.5494C>G (p.Gln1832Glu) rs199473320
NM_198056.2(SCN5A):c.5676C>T (p.Ile1892=) rs763463291
NM_198056.2(SCN5A):c.567T>C (p.Leu189=) rs876657581
NM_198056.2(SCN5A):c.5700C>T (p.His1900=) rs376361103
NM_198056.2(SCN5A):c.5715C>T (p.Ala1905=) rs1553692524
NM_198056.2(SCN5A):c.5733C>T (p.Ala1911=) rs781163189
NM_198056.2(SCN5A):c.5851G>T (p.Val1951Leu) rs41315493
NM_198056.2(SCN5A):c.600G>T (p.Val200=) rs1553605659
NM_198056.2(SCN5A):c.723G>A (p.Gly241=) rs776453610
NM_198056.2(SCN5A):c.75G>A (p.Glu25=) rs772359395
NM_198056.2(SCN5A):c.885G>A (p.Glu295=) rs373342830
NM_198056.2(SCN5A):c.888C>T (p.Ala296=) rs774132896
NM_198056.2(SCN5A):c.93G>A (p.Lys31=) rs1553607621
NM_198056.2(SCN5A):c.942C>T (p.Tyr314=) rs762856442

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.