Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38550888G>ACA433332196SCN5Ac.5481C>T (p.Ala1827=)
c.5484C>T (p.Ala1828=)
c.5430C>T (p.Ala1810=)
c.5322C>T (p.Ala1774=)
c.5385C>T (p.Ala1795=)
c.5355C>T (p.Ala1785=)
c.5427C>T (p.Ala1809=)
dbSNP gnomAD v2
3g.38550888G>CCA433332192SCN5Ac.5481C>G (p.Ala1827=)
c.5484C>G (p.Ala1828=)
c.5430C>G (p.Ala1810=)
c.5322C>G (p.Ala1774=)
c.5385C>G (p.Ala1795=)
c.5355C>G (p.Ala1785=)
c.5427C>G (p.Ala1809=)
3g.38550888G=CA1358556812SCN5Ac.5481C= (p.Ala1827=)
c.5484C= (p.Ala1828=)
c.5430C= (p.Ala1810=)
c.5322C= (p.Ala1774=)
c.5385C= (p.Ala1795=)
c.5355C= (p.Ala1785=)
c.5427C= (p.Ala1809=)
3g.38550888G>TCA433332189SCN5Ac.5481C>A (p.Ala1827=)
c.5484C>A (p.Ala1828=)
c.5430C>A (p.Ala1810=)
c.5322C>A (p.Ala1774=)
c.5385C>A (p.Ala1795=)
c.5355C>A (p.Ala1785=)
c.5427C>A (p.Ala1809=)
3g.38550889G>ACA352141019SCN5Ac.5480C>T (p.Ala1827Val)
c.5483C>T (p.Ala1828Val)
c.5429C>T (p.Ala1810Val)
c.5321C>T (p.Ala1774Val)
c.5384C>T (p.Ala1795Val)
c.5354C>T (p.Ala1785Val)
c.5426C>T (p.Ala1809Val)
3g.38550889G>CCA352141020SCN5Ac.5480C>G (p.Ala1827Gly)
c.5483C>G (p.Ala1828Gly)
c.5429C>G (p.Ala1810Gly)
c.5321C>G (p.Ala1774Gly)
c.5384C>G (p.Ala1795Gly)
c.5354C>G (p.Ala1785Gly)
c.5426C>G (p.Ala1809Gly)
3g.38550889G>TCA352141018SCN5Ac.5480C>A (p.Ala1827Asp)
c.5483C>A (p.Ala1828Asp)
c.5429C>A (p.Ala1810Asp)
c.5321C>A (p.Ala1774Asp)
c.5384C>A (p.Ala1795Asp)
c.5354C>A (p.Ala1785Asp)
c.5426C>A (p.Ala1809Asp)
3g.38550890C>ACA352141021SCN5Ac.5479G>T (p.Ala1827Ser)
c.5482G>T (p.Ala1828Ser)
c.5428G>T (p.Ala1810Ser)
c.5320G>T (p.Ala1774Ser)
c.5383G>T (p.Ala1795Ser)
c.5353G>T (p.Ala1785Ser)
c.5425G>T (p.Ala1809Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38550890C=CA1358556818SCN5Ac.5479G= (p.Ala1827=)
c.5482G= (p.Ala1828=)
c.5428G= (p.Ala1810=)
c.5320G= (p.Ala1774=)
c.5383G= (p.Ala1795=)
c.5353G= (p.Ala1785=)
c.5425G= (p.Ala1809=)
3g.38550890C>GCA352141022SCN5Ac.5479G>C (p.Ala1827Pro)
c.5482G>C (p.Ala1828Pro)
c.5428G>C (p.Ala1810Pro)
c.5320G>C (p.Ala1774Pro)
c.5383G>C (p.Ala1795Pro)
c.5353G>C (p.Ala1785Pro)
c.5425G>C (p.Ala1809Pro)
3g.38550890C>TCA019290SCN5Ac.5479G>A (p.Ala1827Thr)
c.5482G>A (p.Ala1828Thr)
c.5428G>A (p.Ala1810Thr)
c.5320G>A (p.Ala1774Thr)
c.5383G>A (p.Ala1795Thr)
c.5353G>A (p.Ala1785Thr)
c.5425G>A (p.Ala1809Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38550891G>ACA019284SCN5Ac.5478C>T (p.Ile1826=)
c.5481C>T (p.Ile1827=)
c.5427C>T (p.Ile1809=)
c.5319C>T (p.Ile1773=)
c.5382C>T (p.Ile1794=)
c.5352C>T (p.Ile1784=)
c.5424C>T (p.Ile1808=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550891G>CCA352141023SCN5Ac.5478C>G (p.Ile1826Met)
c.5481C>G (p.Ile1827Met)
c.5427C>G (p.Ile1809Met)
c.5319C>G (p.Ile1773Met)
c.5382C>G (p.Ile1794Met)
c.5352C>G (p.Ile1784Met)
c.5424C>G (p.Ile1808Met)
3g.38550891G=CA1358556828SCN5Ac.5478C= (p.Ile1826=)
c.5481C= (p.Ile1827=)
c.5427C= (p.Ile1809=)
c.5319C= (p.Ile1773=)
c.5382C= (p.Ile1794=)
c.5352C= (p.Ile1784=)
c.5424C= (p.Ile1808=)
3g.38550891G>TCA433332214SCN5Ac.5478C>A (p.Ile1826=)
c.5481C>A (p.Ile1827=)
c.5427C>A (p.Ile1809=)
c.5319C>A (p.Ile1773=)
c.5382C>A (p.Ile1794=)
c.5352C>A (p.Ile1784=)
c.5424C>A (p.Ile1808=)
3g.38550892A>CCA352141026SCN5Ac.5477T>G (p.Ile1826Ser)
c.5480T>G (p.Ile1827Ser)
c.5426T>G (p.Ile1809Ser)
c.5318T>G (p.Ile1773Ser)
c.5381T>G (p.Ile1794Ser)
c.5351T>G (p.Ile1784Ser)
c.5423T>G (p.Ile1808Ser)
3g.38550892A>GCA352141025SCN5Ac.5477T>C (p.Ile1826Thr)
c.5480T>C (p.Ile1827Thr)
c.5426T>C (p.Ile1809Thr)
c.5318T>C (p.Ile1773Thr)
c.5381T>C (p.Ile1794Thr)
c.5351T>C (p.Ile1784Thr)
c.5423T>C (p.Ile1808Thr)
3g.38550892A>TCA352141024SCN5Ac.5477T>A (p.Ile1826Asn)
c.5480T>A (p.Ile1827Asn)
c.5426T>A (p.Ile1809Asn)
c.5318T>A (p.Ile1773Asn)
c.5381T>A (p.Ile1794Asn)
c.5351T>A (p.Ile1784Asn)
c.5423T>A (p.Ile1808Asn)
3g.38550893T>ACA352141027SCN5Ac.5476A>T (p.Ile1826Phe)
c.5479A>T (p.Ile1827Phe)
c.5425A>T (p.Ile1809Phe)
c.5317A>T (p.Ile1773Phe)
c.5380A>T (p.Ile1794Phe)
c.5350A>T (p.Ile1784Phe)
c.5422A>T (p.Ile1808Phe)
3g.38550893T>CCA352141028SCN5Ac.5476A>G (p.Ile1826Val)
c.5479A>G (p.Ile1827Val)
c.5425A>G (p.Ile1809Val)
c.5317A>G (p.Ile1773Val)
c.5380A>G (p.Ile1794Val)
c.5350A>G (p.Ile1784Val)
c.5422A>G (p.Ile1808Val)
3g.38550893T>GCA352141029SCN5Ac.5476A>C (p.Ile1826Leu)
c.5479A>C (p.Ile1827Leu)
c.5425A>C (p.Ile1809Leu)
c.5317A>C (p.Ile1773Leu)
c.5380A>C (p.Ile1794Leu)
c.5350A>C (p.Ile1784Leu)
c.5422A>C (p.Ile1808Leu)
3g.38550894A=CA1358556836SCN5Ac.5475T= (p.Arg1825=)
c.5478T= (p.Arg1826=)
c.5424T= (p.Arg1808=)
c.5316T= (p.Arg1772=)
c.5379T= (p.Arg1793=)
c.5349T= (p.Arg1783=)
c.5421T= (p.Arg1807=)
3g.38550894A>CCA433332221SCN5Ac.5475T>G (p.Arg1825=)
c.5478T>G (p.Arg1826=)
c.5424T>G (p.Arg1808=)
c.5316T>G (p.Arg1772=)
c.5379T>G (p.Arg1793=)
c.5349T>G (p.Arg1783=)
c.5421T>G (p.Arg1807=)
3g.38550894A>GCA433332222SCN5Ac.5475T>C (p.Arg1825=)
c.5478T>C (p.Arg1826=)
c.5424T>C (p.Arg1808=)
c.5316T>C (p.Arg1772=)
c.5379T>C (p.Arg1793=)
c.5349T>C (p.Arg1783=)
c.5421T>C (p.Arg1807=)
3g.38550894A>TCA16604908SCN5Ac.5475T>A (p.Arg1825=)
c.5478T>A (p.Arg1826=)
c.5424T>A (p.Arg1808=)
c.5316T>A (p.Arg1772=)
c.5379T>A (p.Arg1793=)
c.5349T>A (p.Arg1783=)
c.5421T>A (p.Arg1807=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38550895C>ACA352141030SCN5Ac.5474G>T (p.Arg1825Leu)
c.5477G>T (p.Arg1826Leu)
c.5423G>T (p.Arg1808Leu)
c.5315G>T (p.Arg1772Leu)
c.5378G>T (p.Arg1793Leu)
c.5348G>T (p.Arg1783Leu)
c.5420G>T (p.Arg1807Leu)
gnomAD v4
3g.38550895C=CA1358556841SCN5Ac.5474G= (p.Arg1825=)
c.5477G= (p.Arg1826=)
c.5423G= (p.Arg1808=)
c.5315G= (p.Arg1772=)
c.5378G= (p.Arg1793=)
c.5348G= (p.Arg1783=)
c.5420G= (p.Arg1807=)
3g.38550895C>GCA352141031SCN5Ac.5474G>C (p.Arg1825Pro)
c.5477G>C (p.Arg1826Pro)
c.5423G>C (p.Arg1808Pro)
c.5315G>C (p.Arg1772Pro)
c.5378G>C (p.Arg1793Pro)
c.5348G>C (p.Arg1783Pro)
c.5420G>C (p.Arg1807Pro)
3g.38550895C>TCA019280SCN5Ac.5474G>A (p.Arg1825His)
c.5477G>A (p.Arg1826His)
c.5423G>A (p.Arg1808His)
c.5315G>A (p.Arg1772His)
c.5378G>A (p.Arg1793His)
c.5348G>A (p.Arg1783His)
c.5420G>A (p.Arg1807His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550896G>ACA019274SCN5Ac.5473C>T (p.Arg1825Cys)
c.5476C>T (p.Arg1826Cys)
c.5422C>T (p.Arg1808Cys)
c.5314C>T (p.Arg1772Cys)
c.5377C>T (p.Arg1793Cys)
c.5347C>T (p.Arg1783Cys)
c.5419C>T (p.Arg1807Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38550896G>CCA352141033SCN5Ac.5473C>G (p.Arg1825Gly)
c.5476C>G (p.Arg1826Gly)
c.5422C>G (p.Arg1808Gly)
c.5314C>G (p.Arg1772Gly)
c.5377C>G (p.Arg1793Gly)
c.5347C>G (p.Arg1783Gly)
c.5419C>G (p.Arg1807Gly)
3g.38550896G=CA1358556848SCN5Ac.5473C= (p.Arg1825=)
c.5476C= (p.Arg1826=)
c.5422C= (p.Arg1808=)
c.5314C= (p.Arg1772=)
c.5377C= (p.Arg1793=)
c.5347C= (p.Arg1783=)
c.5419C= (p.Arg1807=)
3g.38550896G>TCA352141032SCN5Ac.5473C>A (p.Arg1825Ser)
c.5476C>A (p.Arg1826Ser)
c.5422C>A (p.Arg1808Ser)
c.5314C>A (p.Arg1772Ser)
c.5377C>A (p.Arg1793Ser)
c.5347C>A (p.Arg1783Ser)
c.5419C>A (p.Arg1807Ser)
3g.38550897G>ACA433332233SCN5Ac.5472C>T (p.Leu1824=)
c.5475C>T (p.Leu1825=)
c.5421C>T (p.Leu1807=)
c.5313C>T (p.Leu1771=)
c.5376C>T (p.Leu1792=)
c.5346C>T (p.Leu1782=)
c.5418C>T (p.Leu1806=)
ClinVar dbSNP COSMIC COSMIC COSMIC
3g.38550897G>CCA433332235SCN5Ac.5472C>G (p.Leu1824=)
c.5475C>G (p.Leu1825=)
c.5421C>G (p.Leu1807=)
c.5313C>G (p.Leu1771=)
c.5376C>G (p.Leu1792=)
c.5346C>G (p.Leu1782=)
c.5418C>G (p.Leu1806=)
3g.38550897G=CA1358556853SCN5Ac.5472C= (p.Leu1824=)
c.5475C= (p.Leu1825=)
c.5421C= (p.Leu1807=)
c.5313C= (p.Leu1771=)
c.5376C= (p.Leu1792=)
c.5346C= (p.Leu1782=)
c.5418C= (p.Leu1806=)
3g.38550897G>TCA433332237SCN5Ac.5472C>A (p.Leu1824=)
c.5475C>A (p.Leu1825=)
c.5421C>A (p.Leu1807=)
c.5313C>A (p.Leu1771=)
c.5376C>A (p.Leu1792=)
c.5346C>A (p.Leu1782=)
c.5418C>A (p.Leu1806=)
3g.38550898A=CA1358556858SCN5Ac.5471T= (p.Leu1824=)
c.5474T= (p.Leu1825=)
c.5420T= (p.Leu1807=)
c.5312T= (p.Leu1771=)
c.5375T= (p.Leu1792=)
c.5345T= (p.Leu1782=)
c.5417T= (p.Leu1806=)
3g.38550898A>CCA352141034SCN5Ac.5471T>G (p.Leu1824Arg)
c.5474T>G (p.Leu1825Arg)
c.5420T>G (p.Leu1807Arg)
c.5312T>G (p.Leu1771Arg)
c.5375T>G (p.Leu1792Arg)
c.5345T>G (p.Leu1782Arg)
c.5417T>G (p.Leu1806Arg)
3g.38550898A>GCA019266SCN5Ac.5471T>C (p.Leu1824Pro)
c.5474T>C (p.Leu1825Pro)
c.5420T>C (p.Leu1807Pro)
c.5312T>C (p.Leu1771Pro)
c.5375T>C (p.Leu1792Pro)
c.5345T>C (p.Leu1782Pro)
c.5417T>C (p.Leu1806Pro)
ClinVar dbSNP
3g.38550898A>TCA352141035SCN5Ac.5471T>A (p.Leu1824His)
c.5474T>A (p.Leu1825His)
c.5420T>A (p.Leu1807His)
c.5312T>A (p.Leu1771His)
c.5375T>A (p.Leu1792His)
c.5345T>A (p.Leu1782His)
c.5417T>A (p.Leu1806His)
3g.38550899G>ACA352141036SCN5Ac.5470C>T (p.Leu1824Phe)
c.5473C>T (p.Leu1825Phe)
c.5419C>T (p.Leu1807Phe)
c.5311C>T (p.Leu1771Phe)
c.5374C>T (p.Leu1792Phe)
c.5344C>T (p.Leu1782Phe)
c.5416C>T (p.Leu1806Phe)
3g.38550899G>CCA352141037SCN5Ac.5470C>G (p.Leu1824Val)
c.5473C>G (p.Leu1825Val)
c.5419C>G (p.Leu1807Val)
c.5311C>G (p.Leu1771Val)
c.5374C>G (p.Leu1792Val)
c.5344C>G (p.Leu1782Val)
c.5416C>G (p.Leu1806Val)
3g.38550899G>TCA352141038SCN5Ac.5470C>A (p.Leu1824Ile)
c.5473C>A (p.Leu1825Ile)
c.5419C>A (p.Leu1807Ile)
c.5311C>A (p.Leu1771Ile)
c.5374C>A (p.Leu1792Ile)
c.5344C>A (p.Leu1782Ile)
c.5416C>A (p.Leu1806Ile)
3g.38550900T>ACA433332241SCN5Ac.5469A>T (p.Pro1823=)
c.5472A>T (p.Pro1824=)
c.5418A>T (p.Pro1806=)
c.5310A>T (p.Pro1770=)
c.5373A>T (p.Pro1791=)
c.5343A>T (p.Pro1781=)
c.5415A>T (p.Pro1805=)
3g.38550900T>CCA433332254SCN5Ac.5469A>G (p.Pro1823=)
c.5472A>G (p.Pro1824=)
c.5418A>G (p.Pro1806=)
c.5310A>G (p.Pro1770=)
c.5373A>G (p.Pro1791=)
c.5343A>G (p.Pro1781=)
c.5415A>G (p.Pro1805=)
ClinVar
3g.38550900T>GCA433332255SCN5Ac.5469A>C (p.Pro1823=)
c.5472A>C (p.Pro1824=)
c.5418A>C (p.Pro1806=)
c.5310A>C (p.Pro1770=)
c.5373A>C (p.Pro1791=)
c.5343A>C (p.Pro1781=)
c.5415A>C (p.Pro1805=)
dbSNP
3g.38550900T=CA1358556861SCN5Ac.5469A= (p.Pro1823=)
c.5472A= (p.Pro1824=)
c.5418A= (p.Pro1806=)
c.5310A= (p.Pro1770=)
c.5373A= (p.Pro1791=)
c.5343A= (p.Pro1781=)
c.5415A= (p.Pro1805=)
3g.38550901G>ACA352141039SCN5Ac.5468C>T (p.Pro1823Leu)
c.5471C>T (p.Pro1824Leu)
c.5417C>T (p.Pro1806Leu)
c.5309C>T (p.Pro1770Leu)
c.5372C>T (p.Pro1791Leu)
c.5342C>T (p.Pro1781Leu)
c.5414C>T (p.Pro1805Leu)
ClinVar dbSNP
3g.38550901G>CCA352141040SCN5Ac.5468C>G (p.Pro1823Arg)
c.5471C>G (p.Pro1824Arg)
c.5417C>G (p.Pro1806Arg)
c.5309C>G (p.Pro1770Arg)
c.5372C>G (p.Pro1791Arg)
c.5342C>G (p.Pro1781Arg)
c.5414C>G (p.Pro1805Arg)

Number of alleles fetched