Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38550985T>ACA352141225SCN5Ac.5384A>T (p.Glu1795Val)
c.5387A>T (p.Glu1796Val)
c.5333A>T (p.Glu1778Val)
c.5225A>T (p.Glu1742Val)
c.5288A>T (p.Glu1763Val)
c.5258A>T (p.Glu1753Val)
c.5330A>T (p.Glu1777Val)
3g.38550985T>CCA352141226SCN5Ac.5384A>G (p.Glu1795Gly)
c.5387A>G (p.Glu1796Gly)
c.5333A>G (p.Glu1778Gly)
c.5225A>G (p.Glu1742Gly)
c.5288A>G (p.Glu1763Gly)
c.5258A>G (p.Glu1753Gly)
c.5330A>G (p.Glu1777Gly)
3g.38550985T>GCA352141227SCN5Ac.5384A>C (p.Glu1795Ala)
c.5387A>C (p.Glu1796Ala)
c.5333A>C (p.Glu1778Ala)
c.5225A>C (p.Glu1742Ala)
c.5288A>C (p.Glu1763Ala)
c.5258A>C (p.Glu1753Ala)
c.5330A>C (p.Glu1777Ala)
3g.38550986_38550988dupCA025554SCN5Ac.5382_5384dup (p.Tyr1794_Glu1795insAsp)
c.5385_5387dup (p.Tyr1795_Glu1796insAsp)
c.5331_5333dup (p.Tyr1777_Glu1778insAsp)
c.5223_5225dup (p.Tyr1741_Glu1742insAsp)
c.5286_5288dup (p.Tyr1762_Glu1763insAsp)
c.5256_5258dup (p.Tyr1752_Glu1753insAsp)
c.5328_5330dup (p.Tyr1776_Glu1777insAsp)
ClinVar dbSNP
3g.38550986C>ACA352141228SCN5Ac.5383G>T (p.Glu1795Ter)
c.5386G>T (p.Glu1796Ter)
c.5332G>T (p.Glu1778Ter)
c.5224G>T (p.Glu1742Ter)
c.5287G>T (p.Glu1763Ter)
c.5257G>T (p.Glu1753Ter)
c.5329G>T (p.Glu1777Ter)
ClinVar dbSNP
3g.38550986C=CA1358557066SCN5Ac.5383G= (p.Glu1795=)
c.5386G= (p.Glu1796=)
c.5332G= (p.Glu1778=)
c.5224G= (p.Glu1742=)
c.5287G= (p.Glu1763=)
c.5257G= (p.Glu1753=)
c.5329G= (p.Glu1777=)
3g.38550986C>GCA352141229SCN5Ac.5383G>C (p.Glu1795Gln)
c.5386G>C (p.Glu1796Gln)
c.5332G>C (p.Glu1778Gln)
c.5224G>C (p.Glu1742Gln)
c.5287G>C (p.Glu1763Gln)
c.5257G>C (p.Glu1753Gln)
c.5329G>C (p.Glu1777Gln)
3g.38550986C>TCA352141230SCN5Ac.5383G>A (p.Glu1795Lys)
c.5386G>A (p.Glu1796Lys)
c.5332G>A (p.Glu1778Lys)
c.5224G>A (p.Glu1742Lys)
c.5287G>A (p.Glu1763Lys)
c.5257G>A (p.Glu1753Lys)
c.5329G>A (p.Glu1777Lys)
3g.38550986_38550988delinsCATCA1358557065SCN5Ac.5381_5383delinsATG (p.Tyr1794=)
c.5384_5386delinsATG (p.Tyr1795=)
c.5330_5332delinsATG (p.Tyr1777=)
c.5222_5224delinsATG (p.Tyr1741=)
c.5285_5287delinsATG (p.Tyr1762=)
c.5255_5257delinsATG (p.Tyr1752=)
c.5327_5329delinsATG (p.Tyr1776=)
3g.38550987A>CCA352141231SCN5Ac.5382T>G (p.Tyr1794Ter)
c.5385T>G (p.Tyr1795Ter)
c.5331T>G (p.Tyr1777Ter)
c.5223T>G (p.Tyr1741Ter)
c.5286T>G (p.Tyr1762Ter)
c.5256T>G (p.Tyr1752Ter)
c.5328T>G (p.Tyr1776Ter)
gnomAD v4
3g.38550987A>GCA433331787SCN5Ac.5382T>C (p.Tyr1794=)
c.5385T>C (p.Tyr1795=)
c.5331T>C (p.Tyr1777=)
c.5223T>C (p.Tyr1741=)
c.5286T>C (p.Tyr1762=)
c.5256T>C (p.Tyr1752=)
c.5328T>C (p.Tyr1776=)
ClinVar gnomAD v4
3g.38550987A>TCA352141232SCN5Ac.5382T>A (p.Tyr1794Ter)
c.5385T>A (p.Tyr1795Ter)
c.5331T>A (p.Tyr1777Ter)
c.5223T>A (p.Tyr1741Ter)
c.5286T>A (p.Tyr1762Ter)
c.5256T>A (p.Tyr1752Ter)
c.5328T>A (p.Tyr1776Ter)
3g.38550988_38550989delCA891843408SCN5Ac.5381_5382del (p.Tyr1794Ter)
c.5384_5385del (p.Tyr1795Ter)
c.5330_5331del (p.Tyr1777Ter)
c.5222_5223del (p.Tyr1741Ter)
c.5285_5286del (p.Tyr1762Ter)
c.5255_5256del (p.Tyr1752Ter)
c.5327_5328del (p.Tyr1776Ter)
ClinVar dbSNP
3g.38550988T>ACA352141234SCN5Ac.5381A>T (p.Tyr1794Phe)
c.5384A>T (p.Tyr1795Phe)
c.5330A>T (p.Tyr1777Phe)
c.5222A>T (p.Tyr1741Phe)
c.5285A>T (p.Tyr1762Phe)
c.5255A>T (p.Tyr1752Phe)
c.5327A>T (p.Tyr1776Phe)
3g.38550988T>CCA019196SCN5Ac.5381A>G (p.Tyr1794Cys)
c.5384A>G (p.Tyr1795Cys)
c.5330A>G (p.Tyr1777Cys)
c.5222A>G (p.Tyr1741Cys)
c.5285A>G (p.Tyr1762Cys)
c.5255A>G (p.Tyr1752Cys)
c.5327A>G (p.Tyr1776Cys)
ClinVar dbSNP
3g.38550988T>GCA352141233SCN5Ac.5381A>C (p.Tyr1794Ser)
c.5384A>C (p.Tyr1795Ser)
c.5330A>C (p.Tyr1777Ser)
c.5222A>C (p.Tyr1741Ser)
c.5285A>C (p.Tyr1762Ser)
c.5255A>C (p.Tyr1752Ser)
c.5327A>C (p.Tyr1776Ser)
3g.38550988T=CA1358557075SCN5Ac.5381A= (p.Tyr1794=)
c.5384A= (p.Tyr1795=)
c.5330A= (p.Tyr1777=)
c.5222A= (p.Tyr1741=)
c.5285A= (p.Tyr1762=)
c.5255A= (p.Tyr1752=)
c.5327A= (p.Tyr1776=)
3g.38550989A=CA1358557082SCN5Ac.5380T= (p.Tyr1794=)
c.5383T= (p.Tyr1795=)
c.5329T= (p.Tyr1777=)
c.5221T= (p.Tyr1741=)
c.5284T= (p.Tyr1762=)
c.5254T= (p.Tyr1752=)
c.5326T= (p.Tyr1776=)
3g.38550989A>CCA352141235SCN5Ac.5380T>G (p.Tyr1794Asp)
c.5383T>G (p.Tyr1795Asp)
c.5329T>G (p.Tyr1777Asp)
c.5221T>G (p.Tyr1741Asp)
c.5284T>G (p.Tyr1762Asp)
c.5254T>G (p.Tyr1752Asp)
c.5326T>G (p.Tyr1776Asp)
3g.38550989A>GCA019191SCN5Ac.5380T>C (p.Tyr1794His)
c.5383T>C (p.Tyr1795His)
c.5329T>C (p.Tyr1777His)
c.5221T>C (p.Tyr1741His)
c.5284T>C (p.Tyr1762His)
c.5254T>C (p.Tyr1752His)
c.5326T>C (p.Tyr1776His)
ClinVar dbSNP
3g.38550989A>TCA352141236SCN5Ac.5380T>A (p.Tyr1794Asn)
c.5383T>A (p.Tyr1795Asn)
c.5329T>A (p.Tyr1777Asn)
c.5221T>A (p.Tyr1741Asn)
c.5284T>A (p.Tyr1762Asn)
c.5254T>A (p.Tyr1752Asn)
c.5326T>A (p.Tyr1776Asn)
3g.38550990G>ACA433331803SCN5Ac.5379C>T (p.Phe1793=)
c.5382C>T (p.Phe1794=)
c.5328C>T (p.Phe1776=)
c.5220C>T (p.Phe1740=)
c.5283C>T (p.Phe1761=)
c.5253C>T (p.Phe1751=)
c.5325C>T (p.Phe1775=)
3g.38550990G>CCA352141237SCN5Ac.5379C>G (p.Phe1793Leu)
c.5382C>G (p.Phe1794Leu)
c.5328C>G (p.Phe1776Leu)
c.5220C>G (p.Phe1740Leu)
c.5283C>G (p.Phe1761Leu)
c.5253C>G (p.Phe1751Leu)
c.5325C>G (p.Phe1775Leu)
3g.38550990G>TCA352141238SCN5Ac.5379C>A (p.Phe1793Leu)
c.5382C>A (p.Phe1794Leu)
c.5328C>A (p.Phe1776Leu)
c.5220C>A (p.Phe1740Leu)
c.5283C>A (p.Phe1761Leu)
c.5253C>A (p.Phe1751Leu)
c.5325C>A (p.Phe1775Leu)
3g.38550990_38550991delinsGACA1358557086SCN5Ac.5378_5379delinsTC (p.Phe1793=)
c.5381_5382delinsTC (p.Phe1794=)
c.5327_5328delinsTC (p.Phe1776=)
c.5219_5220delinsTC (p.Phe1740=)
c.5282_5283delinsTC (p.Phe1761=)
c.5252_5253delinsTC (p.Phe1751=)
c.5324_5325delinsTC (p.Phe1775=)
3g.38550991A>CCA352141239SCN5Ac.5378T>G (p.Phe1793Cys)
c.5381T>G (p.Phe1794Cys)
c.5327T>G (p.Phe1776Cys)
c.5219T>G (p.Phe1740Cys)
c.5282T>G (p.Phe1761Cys)
c.5252T>G (p.Phe1751Cys)
c.5324T>G (p.Phe1775Cys)
3g.38550991A>GCA352141240SCN5Ac.5378T>C (p.Phe1793Ser)
c.5381T>C (p.Phe1794Ser)
c.5327T>C (p.Phe1776Ser)
c.5219T>C (p.Phe1740Ser)
c.5282T>C (p.Phe1761Ser)
c.5252T>C (p.Phe1751Ser)
c.5324T>C (p.Phe1775Ser)
3g.38550991A>TCA352141241SCN5Ac.5378T>A (p.Phe1793Tyr)
c.5381T>A (p.Phe1794Tyr)
c.5327T>A (p.Phe1776Tyr)
c.5219T>A (p.Phe1740Tyr)
c.5282T>A (p.Phe1761Tyr)
c.5252T>A (p.Phe1751Tyr)
c.5324T>A (p.Phe1775Tyr)
3g.38550992delCA916079918SCN5Ac.5378del (p.Phe1793SerfsTer?)
c.5381del (p.Phe1794SerfsTer?)
c.5327del (p.Phe1776SerfsTer?)
c.5219del (p.Phe1740SerfsTer?)
c.5282del (p.Phe1761SerfsTer?)
c.5252del (p.Phe1751SerfsTer?)
c.5324del (p.Phe1775SerfsTer?)
ClinVar dbSNP
3g.38550992A>CCA352141242SCN5Ac.5377T>G (p.Phe1793Val)
c.5380T>G (p.Phe1794Val)
c.5326T>G (p.Phe1776Val)
c.5218T>G (p.Phe1740Val)
c.5281T>G (p.Phe1761Val)
c.5251T>G (p.Phe1751Val)
c.5323T>G (p.Phe1775Val)
3g.38550992A>GCA352141243SCN5Ac.5377T>C (p.Phe1793Leu)
c.5380T>C (p.Phe1794Leu)
c.5326T>C (p.Phe1776Leu)
c.5218T>C (p.Phe1740Leu)
c.5281T>C (p.Phe1761Leu)
c.5251T>C (p.Phe1751Leu)
c.5323T>C (p.Phe1775Leu)
gnomAD v4
3g.38550992A>TCA352141244SCN5Ac.5377T>A (p.Phe1793Ile)
c.5380T>A (p.Phe1794Ile)
c.5326T>A (p.Phe1776Ile)
c.5218T>A (p.Phe1740Ile)
c.5281T>A (p.Phe1761Ile)
c.5251T>A (p.Phe1751Ile)
c.5323T>A (p.Phe1775Ile)
3g.38550993C>ACA352141247SCN5Ac.5376G>T (p.Met1792Ile)
c.5379G>T (p.Met1793Ile)
c.5325G>T (p.Met1775Ile)
c.5217G>T (p.Met1739Ile)
c.5280G>T (p.Met1760Ile)
c.5250G>T (p.Met1750Ile)
c.5322G>T (p.Met1774Ile)
3g.38550993C=CA1358557091SCN5Ac.5376G= (p.Met1792=)
c.5379G= (p.Met1793=)
c.5325G= (p.Met1775=)
c.5217G= (p.Met1739=)
c.5280G= (p.Met1760=)
c.5250G= (p.Met1750=)
c.5322G= (p.Met1774=)
3g.38550993C>GCA352141246SCN5Ac.5376G>C (p.Met1792Ile)
c.5379G>C (p.Met1793Ile)
c.5325G>C (p.Met1775Ile)
c.5217G>C (p.Met1739Ile)
c.5280G>C (p.Met1760Ile)
c.5250G>C (p.Met1750Ile)
c.5322G>C (p.Met1774Ile)
dbSNP
3g.38550993C>TCA352141245SCN5Ac.5376G>A (p.Met1792Ile)
c.5379G>A (p.Met1793Ile)
c.5325G>A (p.Met1775Ile)
c.5217G>A (p.Met1739Ile)
c.5280G>A (p.Met1760Ile)
c.5250G>A (p.Met1750Ile)
c.5322G>A (p.Met1774Ile)
ClinVar dbSNP
3g.38550994A=CA1358557095SCN5Ac.5375T= (p.Met1792=)
c.5378T= (p.Met1793=)
c.5324T= (p.Met1775=)
c.5216T= (p.Met1739=)
c.5279T= (p.Met1760=)
c.5249T= (p.Met1750=)
c.5321T= (p.Met1774=)
3g.38550994A>CCA352141248SCN5Ac.5375T>G (p.Met1792Arg)
c.5378T>G (p.Met1793Arg)
c.5324T>G (p.Met1775Arg)
c.5216T>G (p.Met1739Arg)
c.5279T>G (p.Met1760Arg)
c.5249T>G (p.Met1750Arg)
c.5321T>G (p.Met1774Arg)
3g.38550994A>GCA352141249SCN5Ac.5375T>C (p.Met1792Thr)
c.5378T>C (p.Met1793Thr)
c.5324T>C (p.Met1775Thr)
c.5216T>C (p.Met1739Thr)
c.5279T>C (p.Met1760Thr)
c.5249T>C (p.Met1750Thr)
c.5321T>C (p.Met1774Thr)
3g.38550994A>TCA019186SCN5Ac.5375T>A (p.Met1792Lys)
c.5378T>A (p.Met1793Lys)
c.5324T>A (p.Met1775Lys)
c.5216T>A (p.Met1739Lys)
c.5279T>A (p.Met1760Lys)
c.5249T>A (p.Met1750Lys)
c.5321T>A (p.Met1774Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38550995T>ACA352141250SCN5Ac.5374A>T (p.Met1792Leu)
c.5377A>T (p.Met1793Leu)
c.5323A>T (p.Met1775Leu)
c.5215A>T (p.Met1739Leu)
c.5278A>T (p.Met1760Leu)
c.5248A>T (p.Met1750Leu)
c.5320A>T (p.Met1774Leu)
3g.38550995T>CCA352141251SCN5Ac.5374A>G (p.Met1792Val)
c.5377A>G (p.Met1793Val)
c.5323A>G (p.Met1775Val)
c.5215A>G (p.Met1739Val)
c.5278A>G (p.Met1760Val)
c.5248A>G (p.Met1750Val)
c.5320A>G (p.Met1774Val)
dbSNP gnomAD v3 gnomAD v4
3g.38550995T>GCA352141252SCN5Ac.5374A>C (p.Met1792Leu)
c.5377A>C (p.Met1793Leu)
c.5323A>C (p.Met1775Leu)
c.5215A>C (p.Met1739Leu)
c.5278A>C (p.Met1760Leu)
c.5248A>C (p.Met1750Leu)
c.5320A>C (p.Met1774Leu)
3g.38550995T=CA1358557098SCN5Ac.5374A= (p.Met1792=)
c.5377A= (p.Met1793=)
c.5323A= (p.Met1775=)
c.5215A= (p.Met1739=)
c.5278A= (p.Met1760=)
c.5248A= (p.Met1750=)
c.5320A= (p.Met1774=)
3g.38550996A=CA1358557101SCN5Ac.5373T= (p.Asp1791=)
c.5376T= (p.Asp1792=)
c.5322T= (p.Asp1774=)
c.5214T= (p.Asp1738=)
c.5277T= (p.Asp1759=)
c.5247T= (p.Asp1749=)
c.5319T= (p.Asp1773=)
3g.38550996A>CCA352141253SCN5Ac.5373T>G (p.Asp1791Glu)
c.5376T>G (p.Asp1792Glu)
c.5322T>G (p.Asp1774Glu)
c.5214T>G (p.Asp1738Glu)
c.5277T>G (p.Asp1759Glu)
c.5247T>G (p.Asp1749Glu)
c.5319T>G (p.Asp1773Glu)
3g.38550996A>GCA433331812SCN5Ac.5373T>C (p.Asp1791=)
c.5376T>C (p.Asp1792=)
c.5322T>C (p.Asp1774=)
c.5214T>C (p.Asp1738=)
c.5277T>C (p.Asp1759=)
c.5247T>C (p.Asp1749=)
c.5319T>C (p.Asp1773=)
gnomAD v4
3g.38550996A>TCA72937945SCN5Ac.5373T>A (p.Asp1791Glu)
c.5376T>A (p.Asp1792Glu)
c.5322T>A (p.Asp1774Glu)
c.5214T>A (p.Asp1738Glu)
c.5277T>A (p.Asp1759Glu)
c.5247T>A (p.Asp1749Glu)
c.5319T>A (p.Asp1773Glu)
dbSNP gnomAD v3 gnomAD v4
3g.38550997T>ACA064366SCN5Ac.5372A>T (p.Asp1791Val)
c.5375A>T (p.Asp1792Val)
c.5321A>T (p.Asp1774Val)
c.5213A>T (p.Asp1738Val)
c.5276A>T (p.Asp1759Val)
c.5246A>T (p.Asp1749Val)
c.5318A>T (p.Asp1773Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38550997T>CCA352141254SCN5Ac.5372A>G (p.Asp1791Gly)
c.5375A>G (p.Asp1792Gly)
c.5321A>G (p.Asp1774Gly)
c.5213A>G (p.Asp1738Gly)
c.5276A>G (p.Asp1759Gly)
c.5246A>G (p.Asp1749Gly)
c.5318A>G (p.Asp1773Gly)
dbSNP gnomAD v4

Number of alleles fetched