Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38598931G>ACA433136868SCN5Ac.2010C>T (p.Thr670=)
c.1881C>T (p.Thr627=)
dbSNP gnomAD v2 gnomAD v4
3g.38598931G>CCA433136870SCN5Ac.2010C>G (p.Thr670=)
c.1881C>G (p.Thr627=)
3g.38598931G=CA1358580770SCN5Ac.2010C= (p.Thr670=)
c.1881C= (p.Thr627=)
3g.38598931G>TCA72932949SCN5Ac.2010C>A (p.Thr670=)
c.1881C>A (p.Thr627=)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38598932G>ACA16611391SCN5Ac.2009C>T (p.Thr670Ile)
c.1880C>T (p.Thr627Ile)
ClinVar dbSNP gnomAD v4
3g.38598932G>CCA352144982SCN5Ac.2009C>G (p.Thr670Ser)
c.1880C>G (p.Thr627Ser)
3g.38598932G=CA1358580776SCN5Ac.2009C= (p.Thr670=)
c.1880C= (p.Thr627=)
3g.38598932G>TCA352144983SCN5Ac.2009C>A (p.Thr670Asn)
c.1880C>A (p.Thr627Asn)
ClinVar dbSNP
3g.38598933T>ACA352144986SCN5Ac.2008A>T (p.Thr670Ser)
c.1879A>T (p.Thr627Ser)
3g.38598933T>CCA352144985SCN5Ac.2008A>G (p.Thr670Ala)
c.1879A>G (p.Thr627Ala)
3g.38598933T>GCA352144984SCN5Ac.2008A>C (p.Thr670Pro)
c.1879A>C (p.Thr627Pro)
3g.38598934G>ACA433136875SCN5Ac.2007C>T (p.Leu669=)
c.1878C>T (p.Leu626=)
3g.38598934G>CCA433136876SCN5Ac.2007C>G (p.Leu669=)
c.1878C>G (p.Leu626=)
3g.38598934G>TCA433136877SCN5Ac.2007C>A (p.Leu669=)
c.1878C>A (p.Leu626=)
3g.38598935A=CA1358580784SCN5Ac.2006T= (p.Leu669=)
c.1877T= (p.Leu626=)
3g.38598935A>CCA352144987SCN5Ac.2006T>G (p.Leu669Arg)
c.1877T>G (p.Leu626Arg)
3g.38598935A>GCA352144988SCN5Ac.2006T>C (p.Leu669Pro)
c.1877T>C (p.Leu626Pro)
ClinVar dbSNP
3g.38598935A>TCA352144989SCN5Ac.2006T>A (p.Leu669His)
c.1877T>A (p.Leu626His)
3g.38598936G>ACA352144990SCN5Ac.2005C>T (p.Leu669Phe)
c.1876C>T (p.Leu626Phe)
3g.38598936G>CCA352144991SCN5Ac.2005C>G (p.Leu669Val)
c.1876C>G (p.Leu626Val)
3g.38598936G>TCA352144992SCN5Ac.2005C>A (p.Leu669Ile)
c.1876C>A (p.Leu626Ile)
3g.38598937G>ACA433136885SCN5Ac.2004C>T (p.Val668=)
c.1875C>T (p.Val625=)
3g.38598937G>CCA433136886SCN5Ac.2004C>G (p.Val668=)
c.1875C>G (p.Val625=)
3g.38598937G>TCA433136887SCN5Ac.2004C>A (p.Val668=)
c.1875C>A (p.Val625=)
3g.38598938A>CCA352144995SCN5Ac.2003T>G (p.Val668Gly)
c.1874T>G (p.Val625Gly)
gnomAD v4
3g.38598938A>GCA352144994SCN5Ac.2003T>C (p.Val668Ala)
c.1874T>C (p.Val625Ala)
3g.38598938A>TCA352144993SCN5Ac.2003T>A (p.Val668Asp)
c.1874T>A (p.Val625Asp)
3g.38598939C>ACA352144996SCN5Ac.2002G>T (p.Val668Phe)
c.1873G>T (p.Val625Phe)
3g.38598939C=CA1358580790SCN5Ac.2002G= (p.Val668=)
c.1873G= (p.Val625=)
3g.38598939C>GCA352144997SCN5Ac.2002G>C (p.Val668Leu)
c.1873G>C (p.Val625Leu)
3g.38598939C>TCA059455SCN5Ac.2002G>A (p.Val668Ile)
c.1873G>A (p.Val625Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.38598944_38598963dupCA2586971902SCN5Ac.1983_2002dup (p.Val668GlyfsTer16)
c.1854_1873dup (p.Val625GlyfsTer16)
3g.38598940G>ACA015714SCN5Ac.2001C>T (p.Ser667=)
c.1872C>T (p.Ser624=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38598940G>CCA352144999SCN5Ac.2001C>G (p.Ser667Arg)
c.1872C>G (p.Ser624Arg)
3g.38598940G=CA1358580796SCN5Ac.2001C= (p.Ser667=)
c.1872C= (p.Ser624=)
3g.38598940G>TCA352144998SCN5Ac.2001C>A (p.Ser667Arg)
c.1872C>A (p.Ser624Arg)
3g.38598941C>ACA352145000SCN5Ac.2000G>T (p.Ser667Ile)
c.1871G>T (p.Ser624Ile)
3g.38598941C=CA1358580801SCN5Ac.2000G= (p.Ser667=)
c.1871G= (p.Ser624=)
3g.38598941C>GCA352145001SCN5Ac.2000G>C (p.Ser667Thr)
c.1871G>C (p.Ser624Thr)
3g.38598941C>TCA352145002SCN5Ac.2000G>A (p.Ser667Asn)
c.1871G>A (p.Ser624Asn)
dbSNP gnomAD v3 gnomAD v4
3g.38598942T>ACA352145003SCN5Ac.1999A>T (p.Ser667Cys)
c.1870A>T (p.Ser624Cys)
3g.38598942T>CCA352145004SCN5Ac.1999A>G (p.Ser667Gly)
c.1870A>G (p.Ser624Gly)
3g.38598942T>GCA352145005SCN5Ac.1999A>C (p.Ser667Arg)
c.1870A>C (p.Ser624Arg)
3g.38598943G>ACA433136899SCN5Ac.1998C>T (p.Val666=)
c.1869C>T (p.Val623=)
3g.38598943G>CCA433136900SCN5Ac.1998C>G (p.Val666=)
c.1869C>G (p.Val623=)
3g.38598943G>TCA433136905SCN5Ac.1998C>A (p.Val666=)
c.1869C>A (p.Val623=)
3g.38598944A>CCA352145006SCN5Ac.1997T>G (p.Val666Gly)
c.1868T>G (p.Val623Gly)
3g.38598944A>GCA352145007SCN5Ac.1997T>C (p.Val666Ala)
c.1868T>C (p.Val623Ala)
ClinVar
3g.38598944A>TCA352145008SCN5Ac.1997T>A (p.Val666Asp)
c.1868T>A (p.Val623Asp)
3g.38598945C>ACA352145009SCN5Ac.1996G>T (p.Val666Phe)
c.1867G>T (p.Val623Phe)
3g.38598945C>GCA352145010SCN5Ac.1996G>C (p.Val666Leu)
c.1867G>C (p.Val623Leu)
3g.38598945C>TCA352145011SCN5Ac.1996G>A (p.Val666Ile)
c.1867G>A (p.Val623Ile)
3g.38598946T>ACA433136909SCN5Ac.1995A>T (p.Ala665=)
c.1866A>T (p.Ala622=)
3g.38598946T>CCA433136912SCN5Ac.1995A>G (p.Ala665=)
c.1866A>G (p.Ala622=)
ClinVar dbSNP gnomAD v4
3g.38598946T>GCA433136910SCN5Ac.1995A>C (p.Ala665=)
c.1866A>C (p.Ala622=)
3g.38598947G>ACA352145012SCN5Ac.1994C>T (p.Ala665Val)
c.1865C>T (p.Ala622Val)
ClinVar gnomAD v4
3g.38598947G>CCA352145014SCN5Ac.1994C>G (p.Ala665Gly)
c.1865C>G (p.Ala622Gly)
3g.38598947G>TCA352145013SCN5Ac.1994C>A (p.Ala665Glu)
c.1865C>A (p.Ala622Glu)
3g.38598948C>ACA015703SCN5Ac.1993G>T (p.Ala665Ser)
c.1864G>T (p.Ala622Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38598948C=CA1358580808SCN5Ac.1993G= (p.Ala665=)
c.1864G= (p.Ala622=)
3g.38598948C>GCA352145015SCN5Ac.1993G>C (p.Ala665Pro)
c.1864G>C (p.Ala622Pro)
3g.38598948C>TCA015693SCN5Ac.1993G>A (p.Ala665Thr)
c.1864G>A (p.Ala622Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38598953_38598963dupCA2586971903SCN5Ac.1983_1993dup (p.Ala665GlyfsTer16)
c.1854_1864dup (p.Ala622GlyfsTer16)
3g.38598949G>ACA059413SCN5Ac.1992C>T (p.Ser664=)
c.1863C>T (p.Ser621=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38598949G>CCA352145016SCN5Ac.1992C>G (p.Ser664Arg)
c.1863C>G (p.Ser621Arg)
3g.38598949G=CA1358580814SCN5Ac.1992C= (p.Ser664=)
c.1863C= (p.Ser621=)
3g.38598949G>TCA352145017SCN5Ac.1992C>A (p.Ser664Arg)
c.1863C>A (p.Ser621Arg)
3g.38598950C>ACA352145018SCN5Ac.1991G>T (p.Ser664Ile)
c.1862G>T (p.Ser621Ile)
3g.38598950C>GCA352145019SCN5Ac.1991G>C (p.Ser664Thr)
c.1862G>C (p.Ser621Thr)
3g.38598950C>TCA352145020SCN5Ac.1991G>A (p.Ser664Asn)
c.1862G>A (p.Ser621Asn)
3g.38598951T>ACA352145022SCN5Ac.1990A>T (p.Ser664Cys)
c.1861A>T (p.Ser621Cys)
3g.38598951T>CCA059406SCN5Ac.1990A>G (p.Ser664Gly)
c.1861A>G (p.Ser621Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38598951T>GCA352145021SCN5Ac.1990A>C (p.Ser664Arg)
c.1861A>C (p.Ser621Arg)
3g.38598951T=CA1358580822SCN5Ac.1990A= (p.Ser664=)
c.1861A= (p.Ser621=)
3g.38598952G>ACA433136926SCN5Ac.1989C>T (p.Leu663=)
c.1860C>T (p.Leu620=)
ClinVar gnomAD v4
3g.38598952G>CCA433136931SCN5Ac.1989C>G (p.Leu663=)
c.1860C>G (p.Leu620=)
3g.38598952G=CA1358580829SCN5Ac.1989C= (p.Leu663=)
c.1860C= (p.Leu620=)
3g.38598952G>TCA433136927SCN5Ac.1989C>A (p.Leu663=)
c.1860C>A (p.Leu620=)
3g.38598953A>CCA352145023SCN5Ac.1988T>G (p.Leu663Arg)
c.1859T>G (p.Leu620Arg)
3g.38598953A>GCA352145024SCN5Ac.1988T>C (p.Leu663Pro)
c.1859T>C (p.Leu620Pro)
3g.38598953A>TCA352145025SCN5Ac.1988T>A (p.Leu663His)
c.1859T>A (p.Leu620His)
3g.38598954G>ACA352145026SCN5Ac.1987C>T (p.Leu663Phe)
c.1858C>T (p.Leu620Phe)
3g.38598954G>CCA352145027SCN5Ac.1987C>G (p.Leu663Val)
c.1858C>G (p.Leu620Val)
3g.38598954G>TCA352145028SCN5Ac.1987C>A (p.Leu663Ile)
c.1858C>A (p.Leu620Ile)
3g.38598955G>ACA433136935SCN5Ac.1986C>T (p.Ala662=)
c.1857C>T (p.Ala619=)
3g.38598955G>CCA433136936SCN5Ac.1986C>G (p.Ala662=)
c.1857C>G (p.Ala619=)
3g.38598955G>TCA433136938SCN5Ac.1986C>A (p.Ala662=)
c.1857C>A (p.Ala619=)
3g.38598956G>ACA352145029SCN5Ac.1985C>T (p.Ala662Val)
c.1856C>T (p.Ala619Val)
3g.38598956G>CCA352145030SCN5Ac.1985C>G (p.Ala662Gly)
c.1856C>G (p.Ala619Gly)
3g.38598956G>TCA352145031SCN5Ac.1985C>A (p.Ala662Asp)
c.1856C>A (p.Ala619Asp)
3g.38598957C>ACA059399SCN5Ac.1984G>T (p.Ala662Ser)
c.1855G>T (p.Ala619Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38598957C=CA1358580834SCN5Ac.1984G= (p.Ala662=)
c.1855G= (p.Ala619=)
3g.38598957C>GCA352145032SCN5Ac.1984G>C (p.Ala662Pro)
c.1855G>C (p.Ala619Pro)
3g.38598957C>TCA352145033SCN5Ac.1984G>A (p.Ala662Thr)
c.1855G>A (p.Ala619Thr)
3g.38598958_38598959insGCTGACTGCGCTGAGGGCCCCA2739292406SCN5Ac.1984_1985insGCCCTCAGCGCAGTCAGCGG (p.Ala662GlyfsTer22)
c.1855_1856insGCCCTCAGCGCAGTCAGCGG (p.Ala619GlyfsTer22)
3g.38598958C>ACA433136942SCN5Ac.1983G>T (p.Arg661=)
c.1854G>T (p.Arg618=)
3g.38598958C>GCA433136943SCN5Ac.1983G>C (p.Arg661=)
c.1854G>C (p.Arg618=)
3g.38598958C>TCA433136945SCN5Ac.1983G>A (p.Arg661=)
c.1854G>A (p.Arg618=)
3g.38598959C>ACA352145035SCN5Ac.1982G>T (p.Arg661Leu)
c.1853G>T (p.Arg618Leu)
3g.38598959C=CA1358580841SCN5Ac.1982G= (p.Arg661=)
c.1853G= (p.Arg618=)
3g.38598959C>GCA352145034SCN5Ac.1982G>C (p.Arg661Pro)
c.1853G>C (p.Arg618Pro)
3g.38598959C>TCA72932963SCN5Ac.1982G>A (p.Arg661Gln)
c.1853G>A (p.Arg618Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38598960G>ACA015679SCN5Ac.1981C>T (p.Arg661Trp)
c.1852C>T (p.Arg618Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38598960G>CCA352145036SCN5Ac.1981C>G (p.Arg661Gly)
c.1852C>G (p.Arg618Gly)
3g.38598960G=CA1358580849SCN5Ac.1981C= (p.Arg661=)
c.1852C= (p.Arg618=)
3g.38598960G>TCA433136951SCN5Ac.1981C>A (p.Arg661=)
c.1852C>A (p.Arg618=)
3g.38598961C>ACA352145037SCN5Ac.1980G>T (p.Gln660His)
c.1851G>T (p.Gln617His)
3g.38598961C=CA1358580853SCN5Ac.1980G= (p.Gln660=)
c.1851G= (p.Gln617=)
3g.38598961C>GCA352145038SCN5Ac.1980G>C (p.Gln660His)
c.1851G>C (p.Gln617His)
ClinVar
3g.38598961C>TCA433136954SCN5Ac.1980G>A (p.Gln660=)
c.1851G>A (p.Gln617=)
dbSNP gnomAD v3 gnomAD v4
3g.38598962T>ACA352145039SCN5Ac.1979A>T (p.Gln660Leu)
c.1850A>T (p.Gln617Leu)
3g.38598962T>CCA352145040SCN5Ac.1979A>G (p.Gln660Arg)
c.1850A>G (p.Gln617Arg)
3g.38598962T>GCA352145041SCN5Ac.1979A>C (p.Gln660Pro)
c.1850A>C (p.Gln617Pro)
3g.38598963G>ACA352145042SCN5Ac.1978C>T (p.Gln660Ter)
c.1849C>T (p.Gln617Ter)
3g.38598963G>CCA352145043SCN5Ac.1978C>G (p.Gln660Glu)
c.1849C>G (p.Gln617Glu)
3g.38598963G>TCA352145044SCN5Ac.1978C>A (p.Gln660Lys)
c.1849C>A (p.Gln617Lys)
3g.38598964C>ACA433136959SCN5Ac.1977G>T (p.Arg659=)
c.1848G>T (p.Arg616=)
gnomAD v4
3g.38598964C>GCA433136961SCN5Ac.1977G>C (p.Arg659=)
c.1848G>C (p.Arg616=)
3g.38598964C>TCA433136962SCN5Ac.1977G>A (p.Arg659=)
c.1848G>A (p.Arg616=)
gnomAD v4
3g.38598965dupCA2840078096SCN5Ac.1977dup (p.Gln660AlafsTer?)
c.1848dup (p.Gln617AlafsTer?)
3g.38598965C>ACA352145045SCN5Ac.1976G>T (p.Arg659Leu)
c.1847G>T (p.Arg616Leu)
3g.38598965C=CA1358580857SCN5Ac.1976G= (p.Arg659=)
c.1847G= (p.Arg616=)
3g.38598965C>GCA352145046SCN5Ac.1976G>C (p.Arg659Pro)
c.1847G>C (p.Arg616Pro)
3g.38598965C>TCA059384SCN5Ac.1976G>A (p.Arg659Gln)
c.1847G>A (p.Arg616Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38598966G>ACA015669SCN5Ac.1975C>T (p.Arg659Trp)
c.1846C>T (p.Arg616Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38598966G>CCA352145047SCN5Ac.1975C>G (p.Arg659Gly)
c.1846C>G (p.Arg616Gly)
3g.38598966G=CA1358580861SCN5Ac.1975C= (p.Arg659=)
c.1846C= (p.Arg616=)
3g.38598966G>TCA433136969SCN5Ac.1975C>A (p.Arg659=)
c.1846C>A (p.Arg616=)
dbSNP
3g.38598967T>ACA433136970SCN5Ac.1974A>T (p.Ala658=)
c.1845A>T (p.Ala615=)
3g.38598967T>CCA433136974SCN5Ac.1974A>G (p.Ala658=)
c.1845A>G (p.Ala615=)
3g.38598967T>GCA433136972SCN5Ac.1974A>C (p.Ala658=)
c.1845A>C (p.Ala615=)
3g.38598968G>ACA059363SCN5Ac.1973C>T (p.Ala658Val)
c.1844C>T (p.Ala615Val)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38598968G>CCA352145048SCN5Ac.1973C>G (p.Ala658Gly)
c.1844C>G (p.Ala615Gly)
3g.38598968G=CA1358580867SCN5Ac.1973C= (p.Ala658=)
c.1844C= (p.Ala615=)
3g.38598968G>TCA352145049SCN5Ac.1973C>A (p.Ala658Glu)
c.1844C>A (p.Ala615Glu)
3g.38598969C>ACA352145050SCN5Ac.1972G>T (p.Ala658Ser)
c.1843G>T (p.Ala615Ser)
ClinVar dbSNP
3g.38598969C=CA1358580872SCN5Ac.1972G= (p.Ala658=)
c.1843G= (p.Ala615=)
3g.38598969C>GCA352145051SCN5Ac.1972G>C (p.Ala658Pro)
c.1843G>C (p.Ala615Pro)
3g.38598969C>TCA352145052SCN5Ac.1972G>A (p.Ala658Thr)
c.1843G>A (p.Ala615Thr)
COSMIC COSMIC COSMIC
3g.38598970T>ACA433136976SCN5Ac.1971A>T (p.Gly657=)
c.1842A>T (p.Gly614=)
3g.38598970T>CCA433136981SCN5Ac.1971A>G (p.Gly657=)
c.1842A>G (p.Gly614=)
3g.38598970T>GCA433136982SCN5Ac.1971A>C (p.Gly657=)
c.1842A>C (p.Gly614=)
3g.38598971C>ACA352145055SCN5Ac.1970G>T (p.Gly657Val)
c.1841G>T (p.Gly614Val)
3g.38598971C>GCA352145054SCN5Ac.1970G>C (p.Gly657Ala)
c.1841G>C (p.Gly614Ala)
3g.38598971C>TCA352145053SCN5Ac.1970G>A (p.Gly657Glu)
c.1841G>A (p.Gly614Glu)
3g.38598972C>ACA352145056SCN5Ac.1969G>T (p.Gly657Ter)
c.1840G>T (p.Gly614Ter)
dbSNP
3g.38598972C=CA1358580877SCN5Ac.1969G= (p.Gly657=)
c.1840G= (p.Gly614=)
3g.38598972C>GCA352145057SCN5Ac.1969G>C (p.Gly657Arg)
c.1840G>C (p.Gly614Arg)
3g.38598972C>TCA352145058SCN5Ac.1969G>A (p.Gly657Arg)
c.1840G>A (p.Gly614Arg)
gnomAD v4
3g.38598973T>ACA433136983SCN5Ac.1968A>T (p.Pro656=)
c.1839A>T (p.Pro613=)
3g.38598973T>CCA433136984SCN5Ac.1968A>G (p.Pro656=)
c.1839A>G (p.Pro613=)
3g.38598973T>GCA433136986SCN5Ac.1968A>C (p.Pro656=)
c.1839A>C (p.Pro613=)
3g.38598974G>ACA015659SCN5Ac.1967C>T (p.Pro656Leu)
c.1838C>T (p.Pro613Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38598974G>CCA352145059SCN5Ac.1967C>G (p.Pro656Arg)
c.1838C>G (p.Pro613Arg)
3g.38598974G=CA1358580881SCN5Ac.1967C= (p.Pro656=)
c.1838C= (p.Pro613=)
3g.38598974G>TCA352145060SCN5Ac.1967C>A (p.Pro656Gln)
c.1838C>A (p.Pro613Gln)
3g.38598975G>ACA352145063SCN5Ac.1966C>T (p.Pro656Ser)
c.1837C>T (p.Pro613Ser)
3g.38598975G>CCA352145061SCN5Ac.1966C>G (p.Pro656Ala)
c.1837C>G (p.Pro613Ala)
ClinVar dbSNP
3g.38598975G>TCA352145062SCN5Ac.1966C>A (p.Pro656Thr)
c.1837C>A (p.Pro613Thr)
3g.38598976C>ACA352145064SCN5Ac.1965G>T (p.Glu655Asp)
c.1836G>T (p.Glu612Asp)
3g.38598976C>GCA352145065SCN5Ac.1965G>C (p.Glu655Asp)
c.1836G>C (p.Glu612Asp)
3g.38598976C>TCA433136990SCN5Ac.1965G>A (p.Glu655=)
c.1836G>A (p.Glu612=)
3g.38598977T>ACA352145066SCN5Ac.1964A>T (p.Glu655Val)
c.1835A>T (p.Glu612Val)
3g.38598977T>CCA352145067SCN5Ac.1964A>G (p.Glu655Gly)
c.1835A>G (p.Glu612Gly)
3g.38598977T>GCA352145068SCN5Ac.1964A>C (p.Glu655Ala)
c.1835A>C (p.Glu612Ala)
3g.38598978C>ACA352145069SCN5Ac.1963G>T (p.Glu655Ter)
c.1834G>T (p.Glu612Ter)
ClinVar dbSNP
3g.38598978C=CA1358580886SCN5Ac.1963G= (p.Glu655=)
c.1834G= (p.Glu612=)
3g.38598978C>GCA352145070SCN5Ac.1963G>C (p.Glu655Gln)
c.1834G>C (p.Glu612Gln)
3g.38598978C>TCA015647SCN5Ac.1963G>A (p.Glu655Lys)
c.1834G>A (p.Glu612Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38598979C>ACA352145071SCN5Ac.1962G>T (p.Glu654Asp)
c.1833G>T (p.Glu611Asp)
3g.38598979C=CA1358580888SCN5Ac.1962G= (p.Glu654=)
c.1833G= (p.Glu611=)
3g.38598979C>GCA352145072SCN5Ac.1962G>C (p.Glu654Asp)
c.1833G>C (p.Glu611Asp)
dbSNP gnomAD v2 gnomAD v4
3g.38598979C>TCA433136991SCN5Ac.1962G>A (p.Glu654=)
c.1833G>A (p.Glu611=)
3g.38598980T>ACA352145073SCN5Ac.1961A>T (p.Glu654Val)
c.1832A>T (p.Glu611Val)
3g.38598980T>CCA352145074SCN5Ac.1961A>G (p.Glu654Gly)
c.1832A>G (p.Glu611Gly)
3g.38598980T>GCA352145075SCN5Ac.1961A>C (p.Glu654Ala)
c.1832A>C (p.Glu611Ala)
3g.38598981C>ACA352145076SCN5Ac.1960G>T (p.Glu654Ter)
c.1831G>T (p.Glu611Ter)
dbSNP
3g.38598981C=CA1358580898SCN5Ac.1960G= (p.Glu654=)
c.1831G= (p.Glu611=)
3g.38598981C>GCA352145077SCN5Ac.1960G>C (p.Glu654Gln)
c.1831G>C (p.Glu611Gln)
dbSNP gnomAD v2 COSMIC COSMIC COSMIC
3g.38598981C>TCA015639SCN5Ac.1960G>A (p.Glu654Lys)
c.1831G>A (p.Glu611Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
3g.38598982G>ACA433136997SCN5Ac.1959C>T (p.Phe653=)
c.1830C>T (p.Phe610=)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
3g.38598982G>CCA352145078SCN5Ac.1959C>G (p.Phe653Leu)
c.1830C>G (p.Phe610Leu)
3g.38598982G=CA1358580905SCN5Ac.1959C= (p.Phe653=)
c.1830C= (p.Phe610=)
3g.38598982G>TCA352145079SCN5Ac.1959C>A (p.Phe653Leu)
c.1830C>A (p.Phe610Leu)
gnomAD v4 COSMIC COSMIC COSMIC
3g.38598983A>CCA352145080SCN5Ac.1958T>G (p.Phe653Cys)
c.1829T>G (p.Phe610Cys)
3g.38598983A>GCA352145081SCN5Ac.1958T>C (p.Phe653Ser)
c.1829T>C (p.Phe610Ser)
3g.38598983A>TCA352145082SCN5Ac.1958T>A (p.Phe653Tyr)
c.1829T>A (p.Phe610Tyr)
3g.38598984A>CCA352145083SCN5Ac.1957T>G (p.Phe653Val)
c.1828T>G (p.Phe610Val)
3g.38598984A>GCA352145084SCN5Ac.1957T>C (p.Phe653Leu)
c.1828T>C (p.Phe610Leu)
3g.38598984A>TCA352145085SCN5Ac.1957T>A (p.Phe653Ile)
c.1828T>A (p.Phe610Ile)
3g.38598985G>ACA433137001SCN5Ac.1956C>T (p.Gly652=)
c.1827C>T (p.Gly609=)
ClinVar dbSNP
3g.38598985G>CCA433137002SCN5Ac.1956C>G (p.Gly652=)
c.1827C>G (p.Gly609=)
3g.38598985G=CA1358580908SCN5Ac.1956C= (p.Gly652=)
c.1827C= (p.Gly609=)
3g.38598985G>TCA433137004SCN5Ac.1956C>A (p.Gly652=)
c.1827C>A (p.Gly609=)
3g.38598986C>ACA352145086SCN5Ac.1955G>T (p.Gly652Val)
c.1826G>T (p.Gly609Val)
ClinVar dbSNP
3g.38598986C=CA1358580913SCN5Ac.1955G= (p.Gly652=)
c.1826G= (p.Gly609=)
3g.38598986C>GCA352145087SCN5Ac.1955G>C (p.Gly652Ala)
c.1826G>C (p.Gly609Ala)
3g.38598986C>TCA059341SCN5Ac.1955G>A (p.Gly652Asp)
c.1826G>A (p.Gly609Asp)
ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
3g.38598987C>ACA352145088SCN5Ac.1954G>T (p.Gly652Cys)
c.1825G>T (p.Gly609Cys)
3g.38598987C=CA1358580918SCN5Ac.1954G= (p.Gly652=)
c.1825G= (p.Gly609=)
3g.38598987C>GCA352145089SCN5Ac.1954G>C (p.Gly652Arg)
c.1825G>C (p.Gly609Arg)
3g.38598987C>TCA352145090SCN5Ac.1954G>A (p.Gly652Ser)
c.1825G>A (p.Gly609Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38598988A=CA1358580920SCN5Ac.1953T= (p.Asp651=)
c.1824T= (p.Asp608=)
3g.38598988A>CCA352145091SCN5Ac.1953T>G (p.Asp651Glu)
c.1824T>G (p.Asp608Glu)
3g.38598988A>GCA433137017SCN5Ac.1953T>C (p.Asp651=)
c.1824T>C (p.Asp608=)
dbSNP gnomAD v2 gnomAD v4
3g.38598988A>TCA72932981SCN5Ac.1953T>A (p.Asp651Glu)
c.1824T>A (p.Asp608Glu)
dbSNP
3g.38598989_38598992delCA2586971904SCN5Ac.1950_1953del (p.Asp651AlafsTer25)
c.1821_1824del (p.Asp608AlafsTer25)
3g.38598989T>ACA352145092SCN5Ac.1952A>T (p.Asp651Val)
c.1823A>T (p.Asp608Val)
3g.38598989T>CCA352145093SCN5Ac.1952A>G (p.Asp651Gly)
c.1823A>G (p.Asp608Gly)
3g.38598989T>GCA352145094SCN5Ac.1952A>C (p.Asp651Ala)
c.1823A>C (p.Asp608Ala)
gnomAD v4
3g.38598990C>ACA352145095SCN5Ac.1951G>T (p.Asp651Tyr)
c.1822G>T (p.Asp608Tyr)
ClinVar
3g.38598990C=CA1358580929SCN5Ac.1951G= (p.Asp651=)
c.1822G= (p.Asp608=)
3g.38598990C>GCA015631SCN5Ac.1951G>C (p.Asp651His)
c.1822G>C (p.Asp608His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38598990C>TCA352145096SCN5Ac.1951G>A (p.Asp651Asn)
c.1822G>A (p.Asp608Asn)
dbSNP gnomAD v4
3g.38598991T>ACA433137027SCN5Ac.1950A>T (p.Val650=)
c.1821A>T (p.Val607=)
3g.38598991T>CCA433137025SCN5Ac.1950A>G (p.Val650=)
c.1821A>G (p.Val607=)
3g.38598991T>GCA433137026SCN5Ac.1950A>C (p.Val650=)
c.1821A>C (p.Val607=)
3g.38598992A=CA1358580931SCN5Ac.1949T= (p.Val650=)
c.1820T= (p.Val607=)
3g.38598992A>CCA352145097SCN5Ac.1949T>G (p.Val650Gly)
c.1820T>G (p.Val607Gly)
3g.38598992A>GCA352145098SCN5Ac.1949T>C (p.Val650Ala)
c.1820T>C (p.Val607Ala)
ClinVar dbSNP
3g.38598992A>TCA352145099SCN5Ac.1949T>A (p.Val650Glu)
c.1820T>A (p.Val607Glu)
3g.38598993C>ACA352145100SCN5Ac.1948G>T (p.Val650Leu)
c.1819G>T (p.Val607Leu)
3g.38598993C>GCA352145101SCN5Ac.1948G>C (p.Val650Leu)
c.1819G>C (p.Val607Leu)
3g.38598993C>TCA352145102SCN5Ac.1948G>A (p.Val650Ile)
c.1819G>A (p.Val607Ile)
3g.38598994A>CCA352145104SCN5Ac.1947T>G (p.Cys649Trp)
c.1818T>G (p.Cys606Trp)
3g.38598994A>GCA433137032SCN5Ac.1947T>C (p.Cys649=)
c.1818T>C (p.Cys606=)
3g.38598994A>TCA352145103SCN5Ac.1947T>A (p.Cys649Ter)
c.1818T>A (p.Cys606Ter)
ClinVar
3g.38598995C>ACA352145105SCN5Ac.1946G>T (p.Cys649Phe)
c.1817G>T (p.Cys606Phe)
3g.38598995C=CA1358580934SCN5Ac.1946G= (p.Cys649=)
c.1817G= (p.Cys606=)
3g.38598995C>GCA352145107SCN5Ac.1946G>C (p.Cys649Ser)
c.1817G>C (p.Cys606Ser)
3g.38598995C>TCA352145106SCN5Ac.1946G>A (p.Cys649Tyr)
c.1817G>A (p.Cys606Tyr)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38598996A=CA1358580938SCN5Ac.1945T= (p.Cys649=)
c.1816T= (p.Cys606=)
3g.38598996A>CCA72932986SCN5Ac.1945T>G (p.Cys649Gly)
c.1816T>G (p.Cys606Gly)
ClinVar dbSNP
3g.38598996A>GCA059318SCN5Ac.1945T>C (p.Cys649Arg)
c.1816T>C (p.Cys606Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38598996A>TCA352145108SCN5Ac.1945T>A (p.Cys649Ser)
c.1816T>A (p.Cys606Ser)
3g.38598997C>ACA433137035SCN5Ac.1944G>T (p.Pro648=)
c.1815G>T (p.Pro605=)
3g.38598997C=CA1358580944SCN5Ac.1944G= (p.Pro648=)
c.1815G= (p.Pro605=)
3g.38598997C>GCA433137042SCN5Ac.1944G>C (p.Pro648=)
c.1815G>C (p.Pro605=)
gnomAD v4
3g.38598997C>TCA059307SCN5Ac.1944G>A (p.Pro648=)
c.1815G>A (p.Pro605=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38598998G>ACA015622SCN5Ac.1943C>T (p.Pro648Leu)
c.1814C>T (p.Pro605Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38598998G>CCA352145109SCN5Ac.1943C>G (p.Pro648Arg)
c.1814C>G (p.Pro605Arg)
3g.38598998G=CA1358580948SCN5Ac.1943C= (p.Pro648=)
c.1814C= (p.Pro605=)
3g.38598998G>TCA352145110SCN5Ac.1943C>A (p.Pro648Gln)
c.1814C>A (p.Pro605Gln)
3g.38598999G>ACA352145111SCN5Ac.1942C>T (p.Pro648Ser)
c.1813C>T (p.Pro605Ser)
ClinVar dbSNP gnomAD v4 COSMIC COSMIC COSMIC
3g.38598999G>CCA352145113SCN5Ac.1942C>G (p.Pro648Ala)
c.1813C>G (p.Pro605Ala)
3g.38598999G=CA1358580955SCN5Ac.1942C= (p.Pro648=)
c.1813C= (p.Pro605=)
3g.38598999G>TCA352145112SCN5Ac.1942C>A (p.Pro648Thr)
c.1813C>A (p.Pro605Thr)
3g.38599000A>CCA433137043SCN5Ac.1941T>G (p.Ala647=)
c.1812T>G (p.Ala604=)
3g.38599000A>GCA433137045SCN5Ac.1941T>C (p.Ala647=)
c.1812T>C (p.Ala604=)
3g.38599000A>TCA433137046SCN5Ac.1941T>A (p.Ala647=)
c.1812T>A (p.Ala604=)
3g.38599001G>ACA015614SCN5Ac.1940C>T (p.Ala647Val)
c.1811C>T (p.Ala604Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38599001G>CCA352145114SCN5Ac.1940C>G (p.Ala647Gly)
c.1811C>G (p.Ala604Gly)
3g.38599001G=CA1358580967SCN5Ac.1940C= (p.Ala647=)
c.1811C= (p.Ala604=)
3g.38599001G>TCA015604SCN5Ac.1940C>A (p.Ala647Asp)
c.1811C>A (p.Ala604Asp)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38599002C>ACA015591SCN5Ac.1939G>T (p.Ala647Ser)
c.1810G>T (p.Ala604Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38599002C=CA1358580976SCN5Ac.1939G= (p.Ala647=)
c.1810G= (p.Ala604=)
3g.38599002C>GCA352145116SCN5Ac.1939G>C (p.Ala647Pro)
c.1810G>C (p.Ala604Pro)
3g.38599002C>TCA352145115SCN5Ac.1939G>A (p.Ala647Thr)
c.1810G>A (p.Ala604Thr)
gnomAD v4
3g.38599003C>ACA352145117SCN5Ac.1938G>T (p.Gln646His)
c.1809G>T (p.Gln603His)
3g.38599003C>GCA352145118SCN5Ac.1938G>C (p.Gln646His)
c.1809G>C (p.Gln603His)
gnomAD v4
3g.38599003C>TCA433137050SCN5Ac.1938G>A (p.Gln646=)
c.1809G>A (p.Gln603=)
gnomAD v4
3g.38599004T>ACA352145119SCN5Ac.1937A>T (p.Gln646Leu)
c.1808A>T (p.Gln603Leu)
3g.38599004T>CCA352145121SCN5Ac.1937A>G (p.Gln646Arg)
c.1808A>G (p.Gln603Arg)
gnomAD v4
3g.38599004T>GCA352145120SCN5Ac.1937A>C (p.Gln646Pro)
c.1808A>C (p.Gln603Pro)
gnomAD v4
3g.38599004_38599005delinsTGCA1358580982SCN5Ac.1936_1937delinsCA (p.Gln646=)
c.1807_1808delinsCA (p.Gln603=)
3g.38599005G>ACA352145122SCN5Ac.1936C>T (p.Gln646Ter)
c.1807C>T (p.Gln603Ter)
3g.38599005G>CCA352145123SCN5Ac.1936C>G (p.Gln646Glu)
c.1807C>G (p.Gln603Glu)
3g.38599005G>TCA352145124SCN5Ac.1936C>A (p.Gln646Lys)
c.1807C>A (p.Gln603Lys)
3g.38599007delCA015579SCN5Ac.1936del (p.Gln646ArgfsTer5)
c.1807del (p.Gln603ArgfsTer5)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38599006G>ACA433137059SCN5Ac.1935C>T (p.Ser645=)
c.1806C>T (p.Ser602=)
3g.38599006G>CCA433137058SCN5Ac.1935C>G (p.Ser645=)
c.1806C>G (p.Ser602=)
3g.38599006G>TCA433137056SCN5Ac.1935C>A (p.Ser645=)
c.1806C>A (p.Ser602=)
gnomAD v4 COSMIC
3g.38599007G>ACA352145125SCN5Ac.1934C>T (p.Ser645Phe)
c.1805C>T (p.Ser602Phe)
3g.38599007G>CCA352145126SCN5Ac.1934C>G (p.Ser645Cys)
c.1805C>G (p.Ser602Cys)
ClinVar dbSNP
3g.38599007G=CA1358580992SCN5Ac.1934C= (p.Ser645=)
c.1805C= (p.Ser602=)
3g.38599007G>TCA352145127SCN5Ac.1934C>A (p.Ser645Tyr)
c.1805C>A (p.Ser602Tyr)
3g.38599008A>CCA352145128SCN5Ac.1933T>G (p.Ser645Ala)
c.1804T>G (p.Ser602Ala)
3g.38599008A>GCA352145129SCN5Ac.1933T>C (p.Ser645Pro)
c.1804T>C (p.Ser602Pro)
3g.38599008A>TCA352145130SCN5Ac.1933T>A (p.Ser645Thr)
c.1804T>A (p.Ser602Thr)
3g.38599009G>ACA433137064SCN5Ac.1932C>T (p.Thr644=)
c.1803C>T (p.Thr601=)
3g.38599009G>CCA433137063SCN5Ac.1932C>G (p.Thr644=)
c.1803C>G (p.Thr601=)
3g.38599009G>TCA433137062SCN5Ac.1932C>A (p.Thr644=)
c.1803C>A (p.Thr601=)
3g.38599010G>ACA352145131SCN5Ac.1931C>T (p.Thr644Ile)
c.1802C>T (p.Thr601Ile)
3g.38599010G>CCA352145132SCN5Ac.1931C>G (p.Thr644Ser)
c.1802C>G (p.Thr601Ser)
3g.38599010G>TCA352145133SCN5Ac.1931C>A (p.Thr644Asn)
c.1802C>A (p.Thr601Asn)
3g.38599011T>ACA352145134SCN5Ac.1930A>T (p.Thr644Ser)
c.1801A>T (p.Thr601Ser)
3g.38599011T>CCA352145135SCN5Ac.1930A>G (p.Thr644Ala)
c.1801A>G (p.Thr601Ala)
3g.38599011T>GCA352145136SCN5Ac.1930A>C (p.Thr644Pro)
c.1801A>C (p.Thr601Pro)
3g.38599012C>ACA433137066SCN5Ac.1929G>T (p.Leu643=)
c.1800G>T (p.Leu600=)
3g.38599012C=CA1358580996SCN5Ac.1929G= (p.Leu643=)
c.1800G= (p.Leu600=)
3g.38599012C>GCA433137070SCN5Ac.1929G>C (p.Leu643=)
c.1800G>C (p.Leu600=)
3g.38599012C>TCA433137068SCN5Ac.1929G>A (p.Leu643=)
c.1800G>A (p.Leu600=)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38599013A>CCA352145137SCN5Ac.1928T>G (p.Leu643Arg)
c.1799T>G (p.Leu600Arg)
3g.38599013A>GCA352145139SCN5Ac.1928T>C (p.Leu643Pro)
c.1799T>C (p.Leu600Pro)
gnomAD v4
3g.38599013A>TCA352145138SCN5Ac.1928T>A (p.Leu643Gln)
c.1799T>A (p.Leu600Gln)
3g.38599014G>ACA10582195SCN5Ac.1927C>T (p.Leu643=)
c.1798C>T (p.Leu600=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38599014G>CCA352145140SCN5Ac.1927C>G (p.Leu643Val)
c.1798C>G (p.Leu600Val)
gnomAD v4
3g.38599014G=CA1358581000SCN5Ac.1927C= (p.Leu643=)
c.1798C= (p.Leu600=)
3g.38599014G>TCA352145141SCN5Ac.1927C>A (p.Leu643Met)
c.1798C>A (p.Leu600Met)
3g.38599015C>ACA352145142SCN5Ac.1926G>T (p.Met642Ile)
c.1797G>T (p.Met599Ile)
gnomAD v4
3g.38599015C>GCA352145143SCN5Ac.1926G>C (p.Met642Ile)
c.1797G>C (p.Met599Ile)
3g.38599015C>TCA352145144SCN5Ac.1926G>A (p.Met642Ile)
c.1797G>A (p.Met599Ile)
3g.38599016A>CCA352145145SCN5Ac.1925T>G (p.Met642Arg)
c.1796T>G (p.Met599Arg)
3g.38599016A>GCA352145146SCN5Ac.1925T>C (p.Met642Thr)
c.1796T>C (p.Met599Thr)
gnomAD v4
3g.38599016A>TCA352145147SCN5Ac.1925T>A (p.Met642Lys)
c.1796T>A (p.Met599Lys)
3g.38599017T>ACA352145150SCN5Ac.1924A>T (p.Met642Leu)
c.1795A>T (p.Met599Leu)
3g.38599017T>CCA352145149SCN5Ac.1924A>G (p.Met642Val)
c.1795A>G (p.Met599Val)
3g.38599017T>GCA352145148SCN5Ac.1924A>C (p.Met642Leu)
c.1795A>C (p.Met599Leu)
3g.38599018C>ACA352145151SCN5Ac.1923G>T (p.Gln641His)
c.1794G>T (p.Gln598His)
3g.38599018C>GCA352145152SCN5Ac.1923G>C (p.Gln641His)
c.1794G>C (p.Gln598His)
3g.38599018C>TCA433137073SCN5Ac.1923G>A (p.Gln641=)
c.1794G>A (p.Gln598=)
ClinVar
3g.38599019T>ACA352145153SCN5Ac.1922A>T (p.Gln641Leu)
c.1793A>T (p.Gln598Leu)
3g.38599019T>CCA352145154SCN5Ac.1922A>G (p.Gln641Arg)
c.1793A>G (p.Gln598Arg)
3g.38599019T>GCA352145155SCN5Ac.1922A>C (p.Gln641Pro)
c.1793A>C (p.Gln598Pro)
3g.38599020G>ACA16617953SCN5Ac.1921C>T (p.Gln641Ter)
c.1792C>T (p.Gln598Ter)
ClinVar dbSNP
3g.38599020G>CCA352145156SCN5Ac.1921C>G (p.Gln641Glu)
c.1792C>G (p.Gln598Glu)
3g.38599020G=CA1358581006SCN5Ac.1921C= (p.Gln641=)
c.1792C= (p.Gln598=)
3g.38599020G>TCA352145157SCN5Ac.1921C>A (p.Gln641Lys)
c.1792C>A (p.Gln598Lys)
3g.38599023delCA2586971906SCN5Ac.1921del (p.Gln641ArgfsTer3)
c.1792del (p.Gln598ArgfsTer3)
3g.38599021G>ACA433137075SCN5Ac.1920C>T (p.Pro640=)
c.1791C>T (p.Pro597=)
COSMIC COSMIC COSMIC
3g.38599021G>CCA433137077SCN5Ac.1920C>G (p.Pro640=)
c.1791C>G (p.Pro597=)
ClinVar dbSNP gnomAD v4
3g.38599021G=CA1358581012SCN5Ac.1920C= (p.Pro640=)
c.1791C= (p.Pro597=)
3g.38599021G>TCA433137078SCN5Ac.1920C>A (p.Pro640=)
c.1791C>A (p.Pro597=)
3g.38599022G>ACA352145158SCN5Ac.1919C>T (p.Pro640Leu)
c.1790C>T (p.Pro597Leu)
ClinVar dbSNP gnomAD v2
3g.38599022G>CCA352145159SCN5Ac.1919C>G (p.Pro640Arg)
c.1790C>G (p.Pro597Arg)
3g.38599022G=CA1358581013SCN5Ac.1919C= (p.Pro640=)
c.1790C= (p.Pro597=)
3g.38599022G>TCA352145160SCN5Ac.1919C>A (p.Pro640His)
c.1790C>A (p.Pro597His)
3g.38599023G>ACA059273SCN5Ac.1918C>T (p.Pro640Ser)
c.1789C>T (p.Pro597Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38599023G>CCA015572SCN5Ac.1918C>G (p.Pro640Ala)
c.1789C>G (p.Pro597Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38599023G=CA1358581015SCN5Ac.1918C= (p.Pro640=)
c.1789C= (p.Pro597=)
3g.38599023G>TCA352145161SCN5Ac.1918C>A (p.Pro640Thr)
c.1789C>A (p.Pro597Thr)
3g.38599024C>ACA433137079SCN5Ac.1917G>T (p.Gly639=)
c.1788G>T (p.Gly596=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38599024C=CA1358581019SCN5Ac.1917G= (p.Gly639=)
c.1788G= (p.Gly596=)
3g.38599024C>GCA433137081SCN5Ac.1917G>C (p.Gly639=)
c.1788G>C (p.Gly596=)
3g.38599024C>TCA433137082SCN5Ac.1917G>A (p.Gly639=)
c.1788G>A (p.Gly596=)
dbSNP
3g.38599025C>ACA352145162SCN5Ac.1916G>T (p.Gly639Val)
c.1787G>T (p.Gly596Val)
3g.38599025C=CA1358581022SCN5Ac.1916G= (p.Gly639=)
c.1787G= (p.Gly596=)
3g.38599025C>GCA352145163SCN5Ac.1916G>C (p.Gly639Ala)
c.1787G>C (p.Gly596Ala)
dbSNP gnomAD v2
3g.38599025C>TCA352145164SCN5Ac.1916G>A (p.Gly639Glu)
c.1787G>A (p.Gly596Glu)
dbSNP
3g.38599027_38599029delCA2839721427SCN5Ac.1914_1916del (p.Gly639del)
c.1785_1787del (p.Gly596del)
3g.38599026C>ACA352145165SCN5Ac.1915G>T (p.Gly639Trp)
c.1786G>T (p.Gly596Trp)
COSMIC
3g.38599026C=CA1358581025SCN5Ac.1915G= (p.Gly639=)
c.1786G= (p.Gly596=)
3g.38599026C>GCA015563SCN5Ac.1915G>C (p.Gly639Arg)
c.1786G>C (p.Gly596Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38599026C>TCA015554SCN5Ac.1915G>A (p.Gly639Arg)
c.1786G>A (p.Gly596Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38599027G>ACA059265SCN5Ac.1914C>T (p.Gly638=)
c.1785C>T (p.Gly595=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38599027G>CCA433137083SCN5Ac.1914C>G (p.Gly638=)
c.1785C>G (p.Gly595=)
gnomAD v4
3g.38599027G=CA1358581034SCN5Ac.1914C= (p.Gly638=)
c.1785C= (p.Gly595=)
3g.38599027G>TCA433137084SCN5Ac.1914C>A (p.Gly638=)
c.1785C>A (p.Gly595=)
ClinVar
3g.38599028C>ACA352145166SCN5Ac.1913G>T (p.Gly638Val)
c.1784G>T (p.Gly595Val)
3g.38599028C=CA1358581043SCN5Ac.1913G= (p.Gly638=)
c.1784G= (p.Gly595=)
3g.38599028C>GCA352145167SCN5Ac.1913G>C (p.Gly638Ala)
c.1784G>C (p.Gly595Ala)
3g.38599028C>TCA015542SCN5Ac.1913G>A (p.Gly638Asp)
c.1784G>A (p.Gly595Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38599029C>ACA352145168SCN5Ac.1912G>T (p.Gly638Cys)
c.1783G>T (p.Gly595Cys)
3g.38599029C>GCA352145169SCN5Ac.1912G>C (p.Gly638Arg)
c.1783G>C (p.Gly595Arg)
3g.38599029C>TCA352145170SCN5Ac.1912G>A (p.Gly638Ser)
c.1783G>A (p.Gly595Ser)
3g.38599030T>ACA433137085SCN5Ac.1911A>T (p.Pro637=)
c.1782A>T (p.Pro594=)
3g.38599030T>CCA059254SCN5Ac.1911A>G (p.Pro637=)
c.1782A>G (p.Pro594=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38599030T>GCA433137087SCN5Ac.1911A>C (p.Pro637=)
c.1782A>C (p.Pro594=)
3g.38599030T=CA1358581046SCN5Ac.1911A= (p.Pro637=)
c.1782A= (p.Pro594=)
3g.38599031G>ACA015533SCN5Ac.1910C>T (p.Pro637Leu)
c.1781C>T (p.Pro594Leu)
ClinVar dbSNP
3g.38599031G>CCA352145171SCN5Ac.1910C>G (p.Pro637Arg)
c.1781C>G (p.Pro594Arg)
3g.38599031G=CA1358581052SCN5Ac.1910C= (p.Pro637=)
c.1781C= (p.Pro594=)
3g.38599031G>TCA352145172SCN5Ac.1910C>A (p.Pro637Gln)
c.1781C>A (p.Pro594Gln)

Number of alleles fetched