Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44907843C>ACA406303302APOEc.127C>A (p.Arg43Ser)
c.205C>A (p.Arg69Ser)
19g.44907843C>GCA406303305APOEc.127C>G (p.Arg43Gly)
c.205C>G (p.Arg69Gly)
19g.44907843C>TCA127525APOEc.127C>T (p.Arg43Cys)
c.205C>T (p.Arg69Cys)
ClinVar dbSNP ExAC gnomAD COSMIC
19g.44907844_44907858delCA9505982APOEc.128_142del (p.Arg43_Ala47del)
c.206_220del (p.Arg69_Ala73del)
dbSNP ExAC gnomAD
19g.44907844G>ACA9505983APOEc.128G>A (p.Arg43His)
c.206G>A (p.Arg69His)
dbSNP ExAC gnomAD
19g.44907844G>CCA406303313APOEc.128G>C (p.Arg43Pro)
c.206G>C (p.Arg69Pro)
19g.44907844G>TCA406303315APOEc.128G>T (p.Arg43Leu)
c.206G>T (p.Arg69Leu)
COSMIC
19g.44907845C>ACA507799007APOEc.129C>A (p.Arg43=)
c.207C>A (p.Arg69=)
19g.44907845C>GCA507799008APOEc.129C>G (p.Arg43=)
c.207C>G (p.Arg69=)
19g.44907845C>TCA9505984APOEc.129C>T (p.Arg43=)
c.207C>T (p.Arg69=)
dbSNP ExAC gnomAD
19g.44907846T>ACA406303321APOEc.130T>A (p.Trp44Arg)
c.208T>A (p.Trp70Arg)
19g.44907846T>CCA406303323APOEc.130T>C (p.Trp44Arg)
c.208T>C (p.Trp70Arg)
19g.44907846T>GCA406303325APOEc.130T>G (p.Trp44Gly)
c.208T>G (p.Trp70Gly)
19g.44907847G>ACA406303329APOEc.131G>A (p.Trp44Ter)
c.209G>A (p.Trp70Ter)
19g.44907847G>CCA406303331APOEc.131G>C (p.Trp44Ser)
c.209G>C (p.Trp70Ser)
19g.44907847G>TCA406303327APOEc.131G>T (p.Trp44Leu)
c.209G>T (p.Trp70Leu)
19g.44907848G>ACA9505985APOEc.132G>A (p.Trp44Ter)
c.210G>A (p.Trp70Ter)
dbSNP ExAC gnomAD
19g.44907848G>CCA406303334APOEc.132G>C (p.Trp44Cys)
c.210G>C (p.Trp70Cys)
19g.44907848G>TCA406303336APOEc.132G>T (p.Trp44Cys)
c.210G>T (p.Trp70Cys)
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>CCA406303344APOEc.134A>C (p.Glu45Ala)
c.212A>C (p.Glu71Ala)
19g.44907850A>GCA406303348APOEc.134A>G (p.Glu45Gly)
c.212A>G (p.Glu71Gly)
19g.44907850A>TCA406303346APOEc.134A>T (p.Glu45Val)
c.212A>T (p.Glu71Val)
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)
19g.44907853T>CCA041808APOEc.137T>C (p.Leu46Pro)
c.215T>C (p.Leu72Pro)
ClinVar dbSNP ExAC gnomAD
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.44907854G>ACA9505986APOEc.138G>A (p.Leu46=)
c.216G>A (p.Leu72=)
dbSNP ExAC gnomAD
19g.44907854G>CCA507799010APOEc.138G>C (p.Leu46=)
c.216G>C (p.Leu72=)
19g.44907854G>TCA507799011APOEc.138G>T (p.Leu46=)
c.216G>T (p.Leu72=)
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)
19g.44907857A>CCA507799013APOEc.141A>C (p.Ala47=)
c.219A>C (p.Ala73=)
19g.44907857A>GCA507799014APOEc.141A>G (p.Ala47=)
c.219A>G (p.Ala73=)
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>GCA406303377APOEc.142C>G (p.Leu48Val)
c.220C>G (p.Leu74Val)
gnomAD
19g.44907858C>TCA507799015APOEc.142C>T (p.Leu48=)
c.220C>T (p.Leu74=)

Number of alleles fetched