Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908867_44908890dupCA633478402APOEc.571_594dup (p.Arg198_Leu199insGlyLeuSerAlaIleArgGluArg)
c.649_672dup (p.Arg224_Leu225insGlyLeuSerAlaIleArgGluArg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908880T>ACA406304308APOEc.584T>A (p.Ile195Asn)
c.662T>A (p.Ile221Asn)
19g.44908880T>CCA406304309APOEc.584T>C (p.Ile195Thr)
c.662T>C (p.Ile221Thr)
19g.44908880T>GCA406304311APOEc.584T>G (p.Ile195Ser)
c.662T>G (p.Ile221Ser)
19g.44908881C>ACA507947394APOEc.585C>A (p.Ile195=)
c.663C>A (p.Ile221=)
19g.44908881C=CA2338167940APOEc.585C= (p.Ile195=)
c.663C= (p.Ile221=)
19g.44908881C>GCA406304312APOEc.585C>G (p.Ile195Met)
c.663C>G (p.Ile221Met)
dbSNP gnomAD v2 gnomAD v4
19g.44908881C>TCA507947396APOEc.585C>T (p.Ile195=)
c.663C>T (p.Ile221=)
dbSNP gnomAD v4
19g.44908882C>ACA406304315APOEc.586C>A (p.Arg196Ser)
c.664C>A (p.Arg222Ser)
gnomAD v4
19g.44908882C=CA2338167941APOEc.586C= (p.Arg196=)
c.664C= (p.Arg222=)
19g.44908882C>GCA406304314APOEc.586C>G (p.Arg196Gly)
c.664C>G (p.Arg222Gly)
19g.44908882C>TCA9506080APOEc.586C>T (p.Arg196Cys)
c.664C>T (p.Arg222Cys)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.44908883G>ACA9506081APOEc.587G>A (p.Arg196His)
c.665G>A (p.Arg222His)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44908883G>CCA406304316APOEc.587G>C (p.Arg196Pro)
c.665G>C (p.Arg222Pro)
gnomAD v4
19g.44908883G=CA2338167942APOEc.587G= (p.Arg196=)
c.665G= (p.Arg222=)
19g.44908883G>TCA406304317APOEc.587G>T (p.Arg196Leu)
c.665G>T (p.Arg222Leu)
gnomAD v4
19g.44908884C>ACA308885886APOEc.588C>A (p.Arg196=)
c.666C>A (p.Arg222=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908884C=CA2338167943APOEc.588C= (p.Arg196=)
c.666C= (p.Arg222=)
19g.44908884C>GCA507947400APOEc.588C>G (p.Arg196=)
c.666C>G (p.Arg222=)
19g.44908884C>TCA507947401APOEc.588C>T (p.Arg196=)
c.666C>T (p.Arg222=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.44908885G>ACA406304319APOEc.589G>A (p.Glu197Lys)
c.667G>A (p.Glu223Lys)
gnomAD v4
19g.44908885G>CCA406304320APOEc.589G>C (p.Glu197Gln)
c.667G>C (p.Glu223Gln)
19g.44908885G>TCA406304322APOEc.589G>T (p.Glu197Ter)
c.667G>T (p.Glu223Ter)
dbSNP gnomAD v4
19g.44908886A=CA2338167944APOEc.590A= (p.Glu197=)
c.668A= (p.Glu223=)
19g.44908886A>CCA406304323APOEc.590A>C (p.Glu197Ala)
c.668A>C (p.Glu223Ala)
19g.44908886A>GCA406304324APOEc.590A>G (p.Glu197Gly)
c.668A>G (p.Glu223Gly)
dbSNP
19g.44908886A>TCA406304325APOEc.590A>T (p.Glu197Val)
c.668A>T (p.Glu223Val)
19g.44908887G>ACA308885887APOEc.591G>A (p.Glu197=)
c.669G>A (p.Glu223=)
ClinVar dbSNP gnomAD v4
19g.44908887G>CCA406304327APOEc.591G>C (p.Glu197Asp)
c.669G>C (p.Glu223Asp)
19g.44908887G=CA2338167945APOEc.591G= (p.Glu197=)
c.669G= (p.Glu223=)
19g.44908887G>TCA406304329APOEc.591G>T (p.Glu197Asp)
c.669G>T (p.Glu223Asp)
19g.44908888C>ACA406304332APOEc.592C>A (p.Arg198Ser)
c.670C>A (p.Arg224Ser)
gnomAD v4
19g.44908888C=CA2338167946APOEc.592C= (p.Arg198=)
c.670C= (p.Arg224=)
19g.44908888C>GCA406304333APOEc.592C>G (p.Arg198Gly)
c.670C>G (p.Arg224Gly)
19g.44908888C>TCA406304331APOEc.592C>T (p.Arg198Cys)
c.670C>T (p.Arg224Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908889G>ACA406304335APOEc.593G>A (p.Arg198His)
c.671G>A (p.Arg224His)
gnomAD v4
19g.44908889G>CCA406304336APOEc.593G>C (p.Arg198Pro)
c.671G>C (p.Arg224Pro)
19g.44908889G=CA2338167947APOEc.593G= (p.Arg198=)
c.671G= (p.Arg224=)
19g.44908889G>TCA308885889APOEc.593G>T (p.Arg198Leu)
c.671G>T (p.Arg224Leu)
dbSNP gnomAD v4
19g.44908890C>ACA507947405APOEc.594C>A (p.Arg198=)
c.672C>A (p.Arg224=)
19g.44908890C=CA2338167948APOEc.594C= (p.Arg198=)
c.672C= (p.Arg224=)
19g.44908890C>GCA507947406APOEc.594C>G (p.Arg198=)
c.672C>G (p.Arg224=)
19g.44908890C>TCA507947407APOEc.594C>T (p.Arg198=)
c.672C>T (p.Arg224=)
dbSNP
19g.44908891C>ACA406304337APOEc.595C>A (p.Leu199Met)
c.673C>A (p.Leu225Met)
19g.44908891C>GCA406304338APOEc.595C>G (p.Leu199Val)
c.673C>G (p.Leu225Val)
19g.44908891C>TCA507947408APOEc.595C>T (p.Leu199=)
c.673C>T (p.Leu225=)
19g.44908891_44908892delCA2695228868APOEc.595_596del (p.Leu199GlyfsTer?)
c.673_674del (p.Leu225GlyfsTer?)
19g.44908892T>ACA406304339APOEc.596T>A (p.Leu199Gln)
c.674T>A (p.Leu225Gln)
19g.44908892T>CCA406304340APOEc.596T>C (p.Leu199Pro)
c.674T>C (p.Leu225Pro)
gnomAD v4
19g.44908892T>GCA308885893APOEc.596T>G (p.Leu199Arg)
c.674T>G (p.Leu225Arg)
dbSNP

Number of alleles fetched