Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38550682C>ACA352140316SCN5Ac.5687G>T (p.Arg1896Leu)
c.5690G>T (p.Arg1897Leu)
c.5636G>T (p.Arg1879Leu)
c.5528G>T (p.Arg1843Leu)
c.5591G>T (p.Arg1864Leu)
c.5561G>T (p.Arg1854Leu)
c.5633G>T (p.Arg1878Leu)
3g.38550682C=CA1358556403SCN5Ac.5687G= (p.Arg1896=)
c.5690G= (p.Arg1897=)
c.5636G= (p.Arg1879=)
c.5528G= (p.Arg1843=)
c.5591G= (p.Arg1864=)
c.5561G= (p.Arg1854=)
c.5633G= (p.Arg1878=)
3g.38550682C>GCA352140318SCN5Ac.5687G>C (p.Arg1896Pro)
c.5690G>C (p.Arg1897Pro)
c.5636G>C (p.Arg1879Pro)
c.5528G>C (p.Arg1843Pro)
c.5591G>C (p.Arg1864Pro)
c.5561G>C (p.Arg1854Pro)
c.5633G>C (p.Arg1878Pro)
3g.38550682C>TCA064637SCN5Ac.5687G>A (p.Arg1896Gln)
c.5690G>A (p.Arg1897Gln)
c.5636G>A (p.Arg1879Gln)
c.5528G>A (p.Arg1843Gln)
c.5591G>A (p.Arg1864Gln)
c.5561G>A (p.Arg1854Gln)
c.5633G>A (p.Arg1878Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38550683G>ACA353758SCN5Ac.5686C>T (p.Arg1896Trp)
c.5689C>T (p.Arg1897Trp)
c.5635C>T (p.Arg1879Trp)
c.5527C>T (p.Arg1843Trp)
c.5590C>T (p.Arg1864Trp)
c.5560C>T (p.Arg1854Trp)
c.5632C>T (p.Arg1878Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38550683G>CCA352140321SCN5Ac.5686C>G (p.Arg1896Gly)
c.5689C>G (p.Arg1897Gly)
c.5635C>G (p.Arg1879Gly)
c.5527C>G (p.Arg1843Gly)
c.5590C>G (p.Arg1864Gly)
c.5560C>G (p.Arg1854Gly)
c.5632C>G (p.Arg1878Gly)
3g.38550683G=CA1358556411SCN5Ac.5686C= (p.Arg1896=)
c.5689C= (p.Arg1897=)
c.5635C= (p.Arg1879=)
c.5527C= (p.Arg1843=)
c.5590C= (p.Arg1864=)
c.5560C= (p.Arg1854=)
c.5632C= (p.Arg1878=)
3g.38550683G>TCA433331617SCN5Ac.5686C>A (p.Arg1896=)
c.5689C>A (p.Arg1897=)
c.5635C>A (p.Arg1879=)
c.5527C>A (p.Arg1843=)
c.5590C>A (p.Arg1864=)
c.5560C>A (p.Arg1854=)
c.5632C>A (p.Arg1878=)
gnomAD v4
3g.38550683_38550685delinsGGACA1358556416SCN5Ac.5684_5686delinsTCC (p.Leu1895=)
c.5687_5689delinsTCC (p.Leu1896=)
c.5633_5635delinsTCC (p.Leu1878=)
c.5525_5527delinsTCC (p.Leu1842=)
c.5588_5590delinsTCC (p.Leu1863=)
c.5558_5560delinsTCC (p.Leu1853=)
c.5630_5632delinsTCC (p.Leu1877=)
3g.38550684G>ACA433331618SCN5Ac.5685C>T (p.Leu1895=)
c.5688C>T (p.Leu1896=)
c.5634C>T (p.Leu1878=)
c.5526C>T (p.Leu1842=)
c.5589C>T (p.Leu1863=)
c.5559C>T (p.Leu1853=)
c.5631C>T (p.Leu1877=)
3g.38550684G>CCA433331619SCN5Ac.5685C>G (p.Leu1895=)
c.5688C>G (p.Leu1896=)
c.5634C>G (p.Leu1878=)
c.5526C>G (p.Leu1842=)
c.5589C>G (p.Leu1863=)
c.5559C>G (p.Leu1853=)
c.5631C>G (p.Leu1877=)
dbSNP
3g.38550684G=CA1358556419SCN5Ac.5685C= (p.Leu1895=)
c.5688C= (p.Leu1896=)
c.5634C= (p.Leu1878=)
c.5526C= (p.Leu1842=)
c.5589C= (p.Leu1863=)
c.5559C= (p.Leu1853=)
c.5631C= (p.Leu1877=)
3g.38550684G>TCA433331620SCN5Ac.5685C>A (p.Leu1895=)
c.5688C>A (p.Leu1896=)
c.5634C>A (p.Leu1878=)
c.5526C>A (p.Leu1842=)
c.5589C>A (p.Leu1863=)
c.5559C>A (p.Leu1853=)
c.5631C>A (p.Leu1877=)
3g.38550685_38550686delCA2319534SCN5Ac.5684_5685del (p.Leu1895ProfsTer?)
c.5687_5688del (p.Leu1896ProfsTer?)
c.5633_5634del (p.Leu1878ProfsTer?)
c.5525_5526del (p.Leu1842ProfsTer?)
c.5588_5589del (p.Leu1863ProfsTer?)
c.5558_5559del (p.Leu1853ProfsTer?)
c.5630_5631del (p.Leu1877ProfsTer?)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38550685A=CA1358556422SCN5Ac.5684T= (p.Leu1895=)
c.5687T= (p.Leu1896=)
c.5633T= (p.Leu1878=)
c.5525T= (p.Leu1842=)
c.5588T= (p.Leu1863=)
c.5558T= (p.Leu1853=)
c.5630T= (p.Leu1877=)
3g.38550685A>CCA352140326SCN5Ac.5684T>G (p.Leu1895Arg)
c.5687T>G (p.Leu1896Arg)
c.5633T>G (p.Leu1878Arg)
c.5525T>G (p.Leu1842Arg)
c.5588T>G (p.Leu1863Arg)
c.5558T>G (p.Leu1853Arg)
c.5630T>G (p.Leu1877Arg)
3g.38550685A>GCA064624SCN5Ac.5684T>C (p.Leu1895Pro)
c.5687T>C (p.Leu1896Pro)
c.5633T>C (p.Leu1878Pro)
c.5525T>C (p.Leu1842Pro)
c.5588T>C (p.Leu1863Pro)
c.5558T>C (p.Leu1853Pro)
c.5630T>C (p.Leu1877Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38550685A>TCA352140323SCN5Ac.5684T>A (p.Leu1895His)
c.5687T>A (p.Leu1896His)
c.5633T>A (p.Leu1878His)
c.5525T>A (p.Leu1842His)
c.5588T>A (p.Leu1863His)
c.5558T>A (p.Leu1853His)
c.5630T>A (p.Leu1877His)
3g.38550686G>ACA352140328SCN5Ac.5683C>T (p.Leu1895Phe)
c.5686C>T (p.Leu1896Phe)
c.5632C>T (p.Leu1878Phe)
c.5524C>T (p.Leu1842Phe)
c.5587C>T (p.Leu1863Phe)
c.5557C>T (p.Leu1853Phe)
c.5629C>T (p.Leu1877Phe)
ClinVar dbSNP
3g.38550686G>CCA352140330SCN5Ac.5683C>G (p.Leu1895Val)
c.5686C>G (p.Leu1896Val)
c.5632C>G (p.Leu1878Val)
c.5524C>G (p.Leu1842Val)
c.5587C>G (p.Leu1863Val)
c.5557C>G (p.Leu1853Val)
c.5629C>G (p.Leu1877Val)
ClinVar
3g.38550686G=CA1358556424SCN5Ac.5683C= (p.Leu1895=)
c.5686C= (p.Leu1896=)
c.5632C= (p.Leu1878=)
c.5524C= (p.Leu1842=)
c.5587C= (p.Leu1863=)
c.5557C= (p.Leu1853=)
c.5629C= (p.Leu1877=)
3g.38550686G>TCA72937844SCN5Ac.5683C>A (p.Leu1895Ile)
c.5686C>A (p.Leu1896Ile)
c.5632C>A (p.Leu1878Ile)
c.5524C>A (p.Leu1842Ile)
c.5587C>A (p.Leu1863Ile)
c.5557C>A (p.Leu1853Ile)
c.5629C>A (p.Leu1877Ile)
dbSNP
3g.38550687T>ACA433331626SCN5Ac.5682A>T (p.Thr1894=)
c.5685A>T (p.Thr1895=)
c.5631A>T (p.Thr1877=)
c.5523A>T (p.Thr1841=)
c.5586A>T (p.Thr1862=)
c.5556A>T (p.Thr1852=)
c.5628A>T (p.Thr1876=)
3g.38550687T>CCA433331627SCN5Ac.5682A>G (p.Thr1894=)
c.5685A>G (p.Thr1895=)
c.5631A>G (p.Thr1877=)
c.5523A>G (p.Thr1841=)
c.5586A>G (p.Thr1862=)
c.5556A>G (p.Thr1852=)
c.5628A>G (p.Thr1876=)
gnomAD v4
3g.38550687T>GCA433331629SCN5Ac.5682A>C (p.Thr1894=)
c.5685A>C (p.Thr1895=)
c.5631A>C (p.Thr1877=)
c.5523A>C (p.Thr1841=)
c.5586A>C (p.Thr1862=)
c.5556A>C (p.Thr1852=)
c.5628A>C (p.Thr1876=)
3g.38550688G>ACA064606SCN5Ac.5681C>T (p.Thr1894Ile)
c.5684C>T (p.Thr1895Ile)
c.5630C>T (p.Thr1877Ile)
c.5522C>T (p.Thr1841Ile)
c.5585C>T (p.Thr1862Ile)
c.5555C>T (p.Thr1852Ile)
c.5627C>T (p.Thr1876Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38550688G>CCA352140334SCN5Ac.5681C>G (p.Thr1894Arg)
c.5684C>G (p.Thr1895Arg)
c.5630C>G (p.Thr1877Arg)
c.5522C>G (p.Thr1841Arg)
c.5585C>G (p.Thr1862Arg)
c.5555C>G (p.Thr1852Arg)
c.5627C>G (p.Thr1876Arg)
3g.38550688G=CA1358556426SCN5Ac.5681C= (p.Thr1894=)
c.5684C= (p.Thr1895=)
c.5630C= (p.Thr1877=)
c.5522C= (p.Thr1841=)
c.5585C= (p.Thr1862=)
c.5555C= (p.Thr1852=)
c.5627C= (p.Thr1876=)
3g.38550688G>TCA352140335SCN5Ac.5681C>A (p.Thr1894Lys)
c.5684C>A (p.Thr1895Lys)
c.5630C>A (p.Thr1877Lys)
c.5522C>A (p.Thr1841Lys)
c.5585C>A (p.Thr1862Lys)
c.5555C>A (p.Thr1852Lys)
c.5627C>A (p.Thr1876Lys)
3g.38550689T>ACA352140338SCN5Ac.5680A>T (p.Thr1894Ser)
c.5683A>T (p.Thr1895Ser)
c.5629A>T (p.Thr1877Ser)
c.5521A>T (p.Thr1841Ser)
c.5584A>T (p.Thr1862Ser)
c.5554A>T (p.Thr1852Ser)
c.5626A>T (p.Thr1876Ser)
3g.38550689T>CCA352140340SCN5Ac.5680A>G (p.Thr1894Ala)
c.5683A>G (p.Thr1895Ala)
c.5629A>G (p.Thr1877Ala)
c.5521A>G (p.Thr1841Ala)
c.5584A>G (p.Thr1862Ala)
c.5554A>G (p.Thr1852Ala)
c.5626A>G (p.Thr1876Ala)
3g.38550689T>GCA352140341SCN5Ac.5680A>C (p.Thr1894Pro)
c.5683A>C (p.Thr1895Pro)
c.5629A>C (p.Thr1877Pro)
c.5521A>C (p.Thr1841Pro)
c.5584A>C (p.Thr1862Pro)
c.5554A>C (p.Thr1852Pro)
c.5626A>C (p.Thr1876Pro)
3g.38550690G>ACA72937846SCN5Ac.5679C>T (p.Thr1893=)
c.5682C>T (p.Thr1894=)
c.5628C>T (p.Thr1876=)
c.5520C>T (p.Thr1840=)
c.5583C>T (p.Thr1861=)
c.5553C>T (p.Thr1851=)
c.5625C>T (p.Thr1875=)
dbSNP gnomAD v4
3g.38550690G>CCA433331633SCN5Ac.5679C>G (p.Thr1893=)
c.5682C>G (p.Thr1894=)
c.5628C>G (p.Thr1876=)
c.5520C>G (p.Thr1840=)
c.5583C>G (p.Thr1861=)
c.5553C>G (p.Thr1851=)
c.5625C>G (p.Thr1875=)
3g.38550690G=CA1358556432SCN5Ac.5679C= (p.Thr1893=)
c.5682C= (p.Thr1894=)
c.5628C= (p.Thr1876=)
c.5520C= (p.Thr1840=)
c.5583C= (p.Thr1861=)
c.5553C= (p.Thr1851=)
c.5625C= (p.Thr1875=)
3g.38550690G>TCA433331634SCN5Ac.5679C>A (p.Thr1893=)
c.5682C>A (p.Thr1894=)
c.5628C>A (p.Thr1876=)
c.5520C>A (p.Thr1840=)
c.5583C>A (p.Thr1861=)
c.5553C>A (p.Thr1851=)
c.5625C>A (p.Thr1875=)
gnomAD v4
3g.38550691G>ACA352140343SCN5Ac.5678C>T (p.Thr1893Ile)
c.5681C>T (p.Thr1894Ile)
c.5627C>T (p.Thr1876Ile)
c.5519C>T (p.Thr1840Ile)
c.5582C>T (p.Thr1861Ile)
c.5552C>T (p.Thr1851Ile)
c.5624C>T (p.Thr1875Ile)
dbSNP
3g.38550691G>CCA352140344SCN5Ac.5678C>G (p.Thr1893Ser)
c.5681C>G (p.Thr1894Ser)
c.5627C>G (p.Thr1876Ser)
c.5519C>G (p.Thr1840Ser)
c.5582C>G (p.Thr1861Ser)
c.5552C>G (p.Thr1851Ser)
c.5624C>G (p.Thr1875Ser)
3g.38550691G=CA1358556435SCN5Ac.5678C= (p.Thr1893=)
c.5681C= (p.Thr1894=)
c.5627C= (p.Thr1876=)
c.5519C= (p.Thr1840=)
c.5582C= (p.Thr1861=)
c.5552C= (p.Thr1851=)
c.5624C= (p.Thr1875=)
3g.38550691G>TCA352140345SCN5Ac.5678C>A (p.Thr1893Asn)
c.5681C>A (p.Thr1894Asn)
c.5627C>A (p.Thr1876Asn)
c.5519C>A (p.Thr1840Asn)
c.5582C>A (p.Thr1861Asn)
c.5552C>A (p.Thr1851Asn)
c.5624C>A (p.Thr1875Asn)
gnomAD v4
3g.38550692T>ACA352140348SCN5Ac.5677A>T (p.Thr1893Ser)
c.5680A>T (p.Thr1894Ser)
c.5626A>T (p.Thr1876Ser)
c.5518A>T (p.Thr1840Ser)
c.5581A>T (p.Thr1861Ser)
c.5551A>T (p.Thr1851Ser)
c.5623A>T (p.Thr1875Ser)
3g.38550692T>CCA352140349SCN5Ac.5677A>G (p.Thr1893Ala)
c.5680A>G (p.Thr1894Ala)
c.5626A>G (p.Thr1876Ala)
c.5518A>G (p.Thr1840Ala)
c.5581A>G (p.Thr1861Ala)
c.5551A>G (p.Thr1851Ala)
c.5623A>G (p.Thr1875Ala)
gnomAD v4
3g.38550692T>GCA352140346SCN5Ac.5677A>C (p.Thr1893Pro)
c.5680A>C (p.Thr1894Pro)
c.5626A>C (p.Thr1876Pro)
c.5518A>C (p.Thr1840Pro)
c.5581A>C (p.Thr1861Pro)
c.5551A>C (p.Thr1851Pro)
c.5623A>C (p.Thr1875Pro)
3g.38550693G>ACA433331646SCN5Ac.5676C>T (p.Thr1892=)
c.5679C>T (p.Thr1893=)
c.5625C>T (p.Thr1875=)
c.5517C>T (p.Thr1839=)
c.5580C>T (p.Thr1860=)
c.5550C>T (p.Thr1850=)
c.5622C>T (p.Thr1874=)
3g.38550693G>CCA433331647SCN5Ac.5676C>G (p.Thr1892=)
c.5679C>G (p.Thr1893=)
c.5625C>G (p.Thr1875=)
c.5517C>G (p.Thr1839=)
c.5580C>G (p.Thr1860=)
c.5550C>G (p.Thr1850=)
c.5622C>G (p.Thr1874=)
3g.38550693G>TCA433331648SCN5Ac.5676C>A (p.Thr1892=)
c.5679C>A (p.Thr1893=)
c.5625C>A (p.Thr1875=)
c.5517C>A (p.Thr1839=)
c.5580C>A (p.Thr1860=)
c.5550C>A (p.Thr1850=)
c.5622C>A (p.Thr1874=)
3g.38550694dupCA2755900437SCN5Ac.5676dup (p.Thr1893HisfsTer?)
c.5679dup (p.Thr1894HisfsTer?)
c.5625dup (p.Thr1876HisfsTer?)
c.5517dup (p.Thr1840HisfsTer?)
c.5580dup (p.Thr1861HisfsTer?)
c.5550dup (p.Thr1851HisfsTer?)
c.5622dup (p.Thr1875HisfsTer?)
3g.38550694G>ACA352140350SCN5Ac.5675C>T (p.Thr1892Ile)
c.5678C>T (p.Thr1893Ile)
c.5624C>T (p.Thr1875Ile)
c.5516C>T (p.Thr1839Ile)
c.5579C>T (p.Thr1860Ile)
c.5549C>T (p.Thr1850Ile)
c.5621C>T (p.Thr1874Ile)
3g.38550694G>CCA352140351SCN5Ac.5675C>G (p.Thr1892Ser)
c.5678C>G (p.Thr1893Ser)
c.5624C>G (p.Thr1875Ser)
c.5516C>G (p.Thr1839Ser)
c.5579C>G (p.Thr1860Ser)
c.5549C>G (p.Thr1850Ser)
c.5621C>G (p.Thr1874Ser)
3g.38550694G=CA1358556437SCN5Ac.5675C= (p.Thr1892=)
c.5678C= (p.Thr1893=)
c.5624C= (p.Thr1875=)
c.5516C= (p.Thr1839=)
c.5579C= (p.Thr1860=)
c.5549C= (p.Thr1850=)
c.5621C= (p.Thr1874=)

Number of alleles fetched