Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44907842_44907857delinsGCGCTGGGAACTGGCACA2338167349APOEc.126_141delinsGCGCTGGGAACTGGCA (p.Gln42=)
c.204_219delinsGCGCTGGGAACTGGCA (p.Gln68=)
19g.44907844_44907858delCA9505982APOEc.128_142del (p.Arg43_Ala47del)
c.206_220del (p.Arg69_Ala73del)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44907849G>ACA406303338APOEc.133G>A (p.Glu45Lys)
c.211G>A (p.Glu71Lys)
19g.44907849G>CCA406303340APOEc.133G>C (p.Glu45Gln)
c.211G>C (p.Glu71Gln)
19g.44907849G>TCA406303342APOEc.133G>T (p.Glu45Ter)
c.211G>T (p.Glu71Ter)
19g.44907850A=CA2338167355APOEc.134A= (p.Glu45=)
c.212A= (p.Glu71=)
19g.44907850A>CCA406303344APOEc.134A>C (p.Glu45Ala)
c.212A>C (p.Glu71Ala)
19g.44907850A>GCA406303348APOEc.134A>G (p.Glu45Gly)
c.212A>G (p.Glu71Gly)
dbSNP
19g.44907850A>TCA406303346APOEc.134A>T (p.Glu45Val)
c.212A>T (p.Glu71Val)
19g.44907851A=CA2338167356APOEc.135A= (p.Glu45=)
c.213A= (p.Glu71=)
19g.44907851A>CCA406303350APOEc.135A>C (p.Glu45Asp)
c.213A>C (p.Glu71Asp)
19g.44907851A>GCA308884513APOEc.135A>G (p.Glu45=)
c.213A>G (p.Glu71=)
dbSNP
19g.44907851A>TCA406303353APOEc.135A>T (p.Glu45Asp)
c.213A>T (p.Glu71Asp)
19g.44907852C>ACA406303355APOEc.136C>A (p.Leu46Met)
c.214C>A (p.Leu72Met)
19g.44907852C>GCA406303358APOEc.136C>G (p.Leu46Val)
c.214C>G (p.Leu72Val)
19g.44907852C>TCA507799009APOEc.136C>T (p.Leu46=)
c.214C>T (p.Leu72=)
19g.44907853T>ACA406303362APOEc.137T>A (p.Leu46Gln)
c.215T>A (p.Leu72Gln)
dbSNP
19g.44907853T>CCA041808APOEc.137T>C (p.Leu46Pro)
c.215T>C (p.Leu72Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.[44907853T>C;44908684T>C]CA041979APOEc.[137T>C;388T>C] (p.[Leu46Pro;Cys130Arg])
c.[215T>C;466T>C] (p.[Leu72Pro;Cys156Arg])
ClinVar
19g.44907853T>GCA406303360APOEc.137T>G (p.Leu46Arg)
c.215T>G (p.Leu72Arg)
19g.44907853T=CA2338167357APOEc.137T= (p.Leu46=)
c.215T= (p.Leu72=)
19g.44907854G>ACA9505986APOEc.138G>A (p.Leu46=)
c.216G>A (p.Leu72=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44907854G>CCA507799010APOEc.138G>C (p.Leu46=)
c.216G>C (p.Leu72=)
19g.44907854G=CA2338167358APOEc.138G= (p.Leu46=)
c.216G= (p.Leu72=)
19g.44907854G>TCA507799011APOEc.138G>T (p.Leu46=)
c.216G>T (p.Leu72=)
19g.44907855delCA2585715223APOEc.139del (p.Ala47HisfsTer?)
c.217del (p.Ala73HisfsTer?)
gnomAD v4
19g.44907855G>ACA406303369APOEc.139G>A (p.Ala47Thr)
c.217G>A (p.Ala73Thr)
COSMIC
19g.44907855G>CCA406303365APOEc.139G>C (p.Ala47Pro)
c.217G>C (p.Ala73Pro)
19g.44907855G>TCA406303367APOEc.139G>T (p.Ala47Ser)
c.217G>T (p.Ala73Ser)
19g.44907856C>ACA406303371APOEc.140C>A (p.Ala47Glu)
c.218C>A (p.Ala73Glu)
19g.44907856C>GCA406303372APOEc.140C>G (p.Ala47Gly)
c.218C>G (p.Ala73Gly)
19g.44907856C>TCA406303374APOEc.140C>T (p.Ala47Val)
c.218C>T (p.Ala73Val)
gnomAD v4
19g.44907857A=CA2338167359APOEc.141A= (p.Ala47=)
c.219A= (p.Ala73=)
19g.44907857A>CCA507799013APOEc.141A>C (p.Ala47=)
c.219A>C (p.Ala73=)
dbSNP
19g.44907857A>GCA507799014APOEc.141A>G (p.Ala47=)
c.219A>G (p.Ala73=)
dbSNP gnomAD v4
19g.44907857A>TCA507799012APOEc.141A>T (p.Ala47=)
c.219A>T (p.Ala73=)
19g.44907858C>ACA406303376APOEc.142C>A (p.Leu48Met)
c.220C>A (p.Leu74Met)
19g.44907858C=CA2338167360APOEc.142C= (p.Leu48=)
c.220C= (p.Leu74=)
19g.44907858C>GCA406303377APOEc.142C>G (p.Leu48Val)
c.220C>G (p.Leu74Val)
dbSNP gnomAD v2 gnomAD v4
19g.44907858C>TCA507799015APOEc.142C>T (p.Leu48=)
c.220C>T (p.Leu74=)
gnomAD v4
19g.44907859T>ACA406303380APOEc.143T>A (p.Leu48Gln)
c.221T>A (p.Leu74Gln)
19g.44907859T>CCA406303384APOEc.143T>C (p.Leu48Pro)
c.221T>C (p.Leu74Pro)
19g.44907859T>GCA406303382APOEc.143T>G (p.Leu48Arg)
c.221T>G (p.Leu74Arg)
19g.44907860G>ACA507799016APOEc.144G>A (p.Leu48=)
c.222G>A (p.Leu74=)
19g.44907860G>CCA308884536APOEc.144G>C (p.Leu48=)
c.222G>C (p.Leu74=)
dbSNP gnomAD v4
19g.44907860G=CA2338167361APOEc.144G= (p.Leu48=)
c.222G= (p.Leu74=)
19g.44907860G>TCA507799017APOEc.144G>T (p.Leu48=)
c.222G>T (p.Leu74=)
19g.44907862delCA2580097377APOEc.146del (p.Gly49ValfsTer30)
c.224del (p.Gly75ValfsTer30)
ClinVar dbSNP
19g.44907861G>ACA406303387APOEc.145G>A (p.Gly49Ser)
c.223G>A (p.Gly75Ser)
dbSNP
19g.44907861G>CCA406303389APOEc.145G>C (p.Gly49Arg)
c.223G>C (p.Gly75Arg)

Number of alleles fetched