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.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)
19g.44907861G=CA2338167362APOEc.145G= (p.Gly49=)
c.223G= (p.Gly75=)
19g.44907861G>TCA406303390APOEc.145G>T (p.Gly49Cys)
c.223G>T (p.Gly75Cys)
19g.44907862G>ACA406303392APOEc.146G>A (p.Gly49Asp)
c.224G>A (p.Gly75Asp)
dbSNP gnomAD v4
19g.44907862G>CCA406303396APOEc.146G>C (p.Gly49Ala)
c.224G>C (p.Gly75Ala)
19g.44907862G=CA2338167363APOEc.146G= (p.Gly49=)
c.224G= (p.Gly75=)
19g.44907862G>TCA406303394APOEc.146G>T (p.Gly49Val)
c.224G>T (p.Gly75Val)
19g.44907863T>ACA507799018APOEc.147T>A (p.Gly49=)
c.225T>A (p.Gly75=)
19g.44907863T>CCA507799019APOEc.147T>C (p.Gly49=)
c.225T>C (p.Gly75=)
dbSNP
19g.44907863T>GCA507799020APOEc.147T>G (p.Gly49=)
c.225T>G (p.Gly75=)
dbSNP
19g.44907863T=CA2338167364APOEc.147T= (p.Gly49=)
c.225T= (p.Gly75=)
19g.44907864C>ACA406303398APOEc.148C>A (p.Arg50Ser)
c.226C>A (p.Arg76Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44907864C=CA2338167365APOEc.148C= (p.Arg50=)
c.226C= (p.Arg76=)
19g.44907864C>GCA9505988APOEc.148C>G (p.Arg50Gly)
c.226C>G (p.Arg76Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44907864C>TCA9505987APOEc.148C>T (p.Arg50Cys)
c.226C>T (p.Arg76Cys)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44907865G>ACA9505991APOEc.149G>A (p.Arg50His)
c.227G>A (p.Arg76His)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44907865G>CCA9505990APOEc.149G>C (p.Arg50Pro)
c.227G>C (p.Arg76Pro)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44907865G=CA2338167366APOEc.149G= (p.Arg50=)
c.227G= (p.Arg76=)
19g.44907865G>TCA9505989APOEc.149G>T (p.Arg50Leu)
c.227G>T (p.Arg76Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44907866C>ACA507799021APOEc.150C>A (p.Arg50=)
c.228C>A (p.Arg76=)
19g.44907866C=CA2338167367APOEc.150C= (p.Arg50=)
c.228C= (p.Arg76=)
19g.44907866C>GCA507799022APOEc.150C>G (p.Arg50=)
c.228C>G (p.Arg76=)
19g.44907866C>TCA9505992APOEc.150C>T (p.Arg50=)
c.228C>T (p.Arg76=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44907867T>ACA406303403APOEc.151T>A (p.Phe51Ile)
c.229T>A (p.Phe77Ile)
gnomAD v4

Number of alleles fetched