Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
3g.38550901G=CA1358556864SCN5Ac.5468C= (p.Pro1823=)
c.5471C= (p.Pro1824=)
c.5417C= (p.Pro1806=)
c.5309C= (p.Pro1770=)
c.5372C= (p.Pro1791=)
c.5342C= (p.Pro1781=)
c.5414C= (p.Pro1805=)
3g.38550901G>TCA352141041SCN5Ac.5468C>A (p.Pro1823Gln)
c.5471C>A (p.Pro1824Gln)
c.5417C>A (p.Pro1806Gln)
c.5309C>A (p.Pro1770Gln)
c.5372C>A (p.Pro1791Gln)
c.5342C>A (p.Pro1781Gln)
c.5414C>A (p.Pro1805Gln)
3g.38550902G>ACA352141042SCN5Ac.5467C>T (p.Pro1823Ser)
c.5470C>T (p.Pro1824Ser)
c.5416C>T (p.Pro1806Ser)
c.5308C>T (p.Pro1770Ser)
c.5371C>T (p.Pro1791Ser)
c.5341C>T (p.Pro1781Ser)
c.5413C>T (p.Pro1805Ser)
3g.38550902G>CCA019262SCN5Ac.5467C>G (p.Pro1823Ala)
c.5470C>G (p.Pro1824Ala)
c.5416C>G (p.Pro1806Ala)
c.5308C>G (p.Pro1770Ala)
c.5371C>G (p.Pro1791Ala)
c.5341C>G (p.Pro1781Ala)
c.5413C>G (p.Pro1805Ala)
ClinVar dbSNP gnomAD v4
3g.38550902G=CA1358556867SCN5Ac.5467C= (p.Pro1823=)
c.5470C= (p.Pro1824=)
c.5416C= (p.Pro1806=)
c.5308C= (p.Pro1770=)
c.5371C= (p.Pro1791=)
c.5341C= (p.Pro1781=)
c.5413C= (p.Pro1805=)
3g.38550902G>TCA352141043SCN5Ac.5467C>A (p.Pro1823Thr)
c.5470C>A (p.Pro1824Thr)
c.5416C>A (p.Pro1806Thr)
c.5308C>A (p.Pro1770Thr)
c.5371C>A (p.Pro1791Thr)
c.5341C>A (p.Pro1781Thr)
c.5413C>A (p.Pro1805Thr)
gnomAD v4
3g.38550903C>ACA352141045SCN5Ac.5466G>T (p.Glu1822Asp)
c.5469G>T (p.Glu1823Asp)
c.5415G>T (p.Glu1805Asp)
c.5307G>T (p.Glu1769Asp)
c.5370G>T (p.Glu1790Asp)
c.5340G>T (p.Glu1780Asp)
c.5412G>T (p.Glu1804Asp)
3g.38550903C>GCA352141044SCN5Ac.5466G>C (p.Glu1822Asp)
c.5469G>C (p.Glu1823Asp)
c.5415G>C (p.Glu1805Asp)
c.5307G>C (p.Glu1769Asp)
c.5370G>C (p.Glu1790Asp)
c.5340G>C (p.Glu1780Asp)
c.5412G>C (p.Glu1804Asp)
3g.38550903C>TCA433332264SCN5Ac.5466G>A (p.Glu1822=)
c.5469G>A (p.Glu1823=)
c.5415G>A (p.Glu1805=)
c.5307G>A (p.Glu1769=)
c.5370G>A (p.Glu1790=)
c.5340G>A (p.Glu1780=)
c.5412G>A (p.Glu1804=)
3g.38550904T>ACA352141046SCN5Ac.5465A>T (p.Glu1822Val)
c.5468A>T (p.Glu1823Val)
c.5414A>T (p.Glu1805Val)
c.5306A>T (p.Glu1769Val)
c.5369A>T (p.Glu1790Val)
c.5339A>T (p.Glu1780Val)
c.5411A>T (p.Glu1804Val)
3g.38550904T>CCA352141048SCN5Ac.5465A>G (p.Glu1822Gly)
c.5468A>G (p.Glu1823Gly)
c.5414A>G (p.Glu1805Gly)
c.5306A>G (p.Glu1769Gly)
c.5369A>G (p.Glu1790Gly)
c.5339A>G (p.Glu1780Gly)
c.5411A>G (p.Glu1804Gly)
3g.38550904T>GCA352141047SCN5Ac.5465A>C (p.Glu1822Ala)
c.5468A>C (p.Glu1823Ala)
c.5414A>C (p.Glu1805Ala)
c.5306A>C (p.Glu1769Ala)
c.5369A>C (p.Glu1790Ala)
c.5339A>C (p.Glu1780Ala)
c.5411A>C (p.Glu1804Ala)
3g.38550904_38550908delinsTCAGACA1358556870SCN5Ac.5461_5465delinsTCTGA (p.Ser1821=)
c.5464_5468delinsTCTGA (p.Ser1822=)
c.5410_5414delinsTCTGA (p.Ser1804=)
c.5302_5306delinsTCTGA (p.Ser1768=)
c.5365_5369delinsTCTGA (p.Ser1789=)
c.5335_5339delinsTCTGA (p.Ser1779=)
c.5407_5411delinsTCTGA (p.Ser1803=)
3g.38550905C>ACA352141049SCN5Ac.5464G>T (p.Glu1822Ter)
c.5467G>T (p.Glu1823Ter)
c.5413G>T (p.Glu1805Ter)
c.5305G>T (p.Glu1769Ter)
c.5368G>T (p.Glu1790Ter)
c.5338G>T (p.Glu1780Ter)
c.5410G>T (p.Glu1804Ter)
3g.38550905C=CA1358556876SCN5Ac.5464G= (p.Glu1822=)
c.5467G= (p.Glu1823=)
c.5413G= (p.Glu1805=)
c.5305G= (p.Glu1769=)
c.5368G= (p.Glu1790=)
c.5338G= (p.Glu1780=)
c.5410G= (p.Glu1804=)
3g.38550905C>GCA352141050SCN5Ac.5464G>C (p.Glu1822Gln)
c.5467G>C (p.Glu1823Gln)
c.5413G>C (p.Glu1805Gln)
c.5305G>C (p.Glu1769Gln)
c.5368G>C (p.Glu1790Gln)
c.5338G>C (p.Glu1780Gln)
c.5410G>C (p.Glu1804Gln)
gnomAD v4
3g.38550905C>TCA064452SCN5Ac.5464G>A (p.Glu1822Lys)
c.5467G>A (p.Glu1823Lys)
c.5413G>A (p.Glu1805Lys)
c.5305G>A (p.Glu1769Lys)
c.5368G>A (p.Glu1790Lys)
c.5338G>A (p.Glu1780Lys)
c.5410G>A (p.Glu1804Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550908_38550911delCA019255SCN5Ac.5461_5464del (p.Glu1822HisfsTer10)
c.5464_5467del (p.Glu1823HisfsTer10)
c.5410_5413del (p.Glu1805HisfsTer10)
c.5302_5305del (p.Glu1769HisfsTer10)
c.5365_5368del (p.Glu1790HisfsTer10)
c.5335_5338del (p.Glu1780HisfsTer10)
c.5407_5410del (p.Glu1804HisfsTer10)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38550906A>CCA433332269SCN5Ac.5463T>G (p.Ser1821=)
c.5466T>G (p.Ser1822=)
c.5412T>G (p.Ser1804=)
c.5304T>G (p.Ser1768=)
c.5367T>G (p.Ser1789=)
c.5337T>G (p.Ser1779=)
c.5409T>G (p.Ser1803=)
3g.38550906A>GCA433332270SCN5Ac.5463T>C (p.Ser1821=)
c.5466T>C (p.Ser1822=)
c.5412T>C (p.Ser1804=)
c.5304T>C (p.Ser1768=)
c.5367T>C (p.Ser1789=)
c.5337T>C (p.Ser1779=)
c.5409T>C (p.Ser1803=)
3g.38550906A>TCA433332272SCN5Ac.5463T>A (p.Ser1821=)
c.5466T>A (p.Ser1822=)
c.5412T>A (p.Ser1804=)
c.5304T>A (p.Ser1768=)
c.5367T>A (p.Ser1789=)
c.5337T>A (p.Ser1779=)
c.5409T>A (p.Ser1803=)
3g.38550907G>ACA352141051SCN5Ac.5462C>T (p.Ser1821Phe)
c.5465C>T (p.Ser1822Phe)
c.5411C>T (p.Ser1804Phe)
c.5303C>T (p.Ser1768Phe)
c.5366C>T (p.Ser1789Phe)
c.5336C>T (p.Ser1779Phe)
c.5408C>T (p.Ser1803Phe)
3g.38550907G>CCA352141052SCN5Ac.5462C>G (p.Ser1821Cys)
c.5465C>G (p.Ser1822Cys)
c.5411C>G (p.Ser1804Cys)
c.5303C>G (p.Ser1768Cys)
c.5366C>G (p.Ser1789Cys)
c.5336C>G (p.Ser1779Cys)
c.5408C>G (p.Ser1803Cys)
3g.38550907G>TCA352141053SCN5Ac.5462C>A (p.Ser1821Tyr)
c.5465C>A (p.Ser1822Tyr)
c.5411C>A (p.Ser1804Tyr)
c.5303C>A (p.Ser1768Tyr)
c.5366C>A (p.Ser1789Tyr)
c.5336C>A (p.Ser1779Tyr)
c.5408C>A (p.Ser1803Tyr)
3g.38550908A>CCA352141054SCN5Ac.5461T>G (p.Ser1821Ala)
c.5464T>G (p.Ser1822Ala)
c.5410T>G (p.Ser1804Ala)
c.5302T>G (p.Ser1768Ala)
c.5365T>G (p.Ser1789Ala)
c.5335T>G (p.Ser1779Ala)
c.5407T>G (p.Ser1803Ala)

Number of alleles fetched