Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908817_44908870delCA2695228866APOEc.521_574del (p.Gln174_Gly191del)
c.599_652del (p.Gln200_Gly217del)
19g.44908855_44908859delCA2585715448APOEc.559_563del (p.Gly187ArgfsTer?)
c.637_641del (p.Gly213ArgfsTer?)
gnomAD v4
19g.44908859C>ACA406304264APOEc.563C>A (p.Ala188Asp)
c.641C>A (p.Ala214Asp)
gnomAD v4
19g.44908859C=CA2338167928APOEc.563C= (p.Ala188=)
c.641C= (p.Ala214=)
19g.44908859C>GCA406304265APOEc.563C>G (p.Ala188Gly)
c.641C>G (p.Ala214Gly)
19g.44908859C>TCA406304263APOEc.563C>T (p.Ala188Val)
c.641C>T (p.Ala214Val)
gnomAD v4
19g.44908860C>ACA507947369APOEc.564C>A (p.Ala188=)
c.642C>A (p.Ala214=)
gnomAD v4
19g.44908860C>GCA507947370APOEc.564C>G (p.Ala188=)
c.642C>G (p.Ala214=)
19g.44908860C>TCA507947371APOEc.564C>T (p.Ala188=)
c.642C>T (p.Ala214=)
gnomAD v4
19g.44908867_44908890dupCA633478402APOEc.571_594dup (p.Arg198_Leu199insGlyLeuSerAlaIleArgGluArg)
c.649_672dup (p.Arg224_Leu225insGlyLeuSerAlaIleArgGluArg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908861G>ACA308885826APOEc.565G>A (p.Glu189Lys)
c.643G>A (p.Glu215Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908861G>CCA406304266APOEc.565G>C (p.Glu189Gln)
c.643G>C (p.Glu215Gln)
dbSNP gnomAD v3 gnomAD v4
19g.44908861G=CA2338167929APOEc.565G= (p.Glu189=)
c.643G= (p.Glu215=)
19g.44908861G>TCA406304267APOEc.565G>T (p.Glu189Ter)
c.643G>T (p.Glu215Ter)
dbSNP gnomAD v4
19g.44908862A=CA2338167930APOEc.566A= (p.Glu189=)
c.644A= (p.Glu215=)
19g.44908862A>CCA406304268APOEc.566A>C (p.Glu189Ala)
c.644A>C (p.Glu215Ala)
19g.44908862A>GCA406304269APOEc.566A>G (p.Glu189Gly)
c.644A>G (p.Glu215Gly)
gnomAD v4
19g.44908862A>TCA406304270APOEc.566A>T (p.Glu189Val)
c.644A>T (p.Glu215Val)
dbSNP gnomAD v3 gnomAD v4
19g.44908863G>ACA507947373APOEc.567G>A (p.Glu189=)
c.645G>A (p.Glu215=)
gnomAD v4
19g.44908863G>CCA406304272APOEc.567G>C (p.Glu189Asp)
c.645G>C (p.Glu215Asp)
19g.44908863G>TCA406304271APOEc.567G>T (p.Glu189Asp)
c.645G>T (p.Glu215Asp)
gnomAD v4
19g.44908864C>ACA406304273APOEc.568C>A (p.Arg190Ser)
c.646C>A (p.Arg216Ser)
gnomAD v4
19g.44908864C=CA2338167931APOEc.568C= (p.Arg190=)
c.646C= (p.Arg216=)
19g.44908864C>GCA406304274APOEc.568C>G (p.Arg190Gly)
c.646C>G (p.Arg216Gly)
19g.44908864C>TCA308885840APOEc.568C>T (p.Arg190Cys)
c.646C>T (p.Arg216Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908865G>ACA406304275APOEc.569G>A (p.Arg190His)
c.647G>A (p.Arg216His)
gnomAD v4
19g.44908865G>CCA406304276APOEc.569G>C (p.Arg190Pro)
c.647G>C (p.Arg216Pro)
19g.44908865G>TCA406304277APOEc.569G>T (p.Arg190Leu)
c.647G>T (p.Arg216Leu)
19g.44908866C>ACA507947374APOEc.570C>A (p.Arg190=)
c.648C>A (p.Arg216=)
19g.44908866C=CA2338167932APOEc.570C= (p.Arg190=)
c.648C= (p.Arg216=)
19g.44908866C>GCA507947375APOEc.570C>G (p.Arg190=)
c.648C>G (p.Arg216=)
19g.44908866C>TCA507947376APOEc.570C>T (p.Arg190=)
c.648C>T (p.Arg216=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.44908867G>ACA406304278APOEc.571G>A (p.Gly191Ser)
c.649G>A (p.Gly217Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908867G>CCA406304280APOEc.571G>C (p.Gly191Arg)
c.649G>C (p.Gly217Arg)
19g.44908867G=CA2338167933APOEc.571G= (p.Gly191=)
c.649G= (p.Gly217=)
19g.44908867G>TCA406304279APOEc.571G>T (p.Gly191Cys)
c.649G>T (p.Gly217Cys)
gnomAD v4
19g.44908868G>ACA406304281APOEc.572G>A (p.Gly191Asp)
c.650G>A (p.Gly217Asp)
gnomAD v4
19g.44908868G>CCA406304282APOEc.572G>C (p.Gly191Ala)
c.650G>C (p.Gly217Ala)
19g.44908868G>TCA406304283APOEc.572G>T (p.Gly191Val)
c.650G>T (p.Gly217Val)
19g.44908869C>ACA507947377APOEc.573C>A (p.Gly191=)
c.651C>A (p.Gly217=)
gnomAD v4
19g.44908869C=CA2338167934APOEc.573C= (p.Gly191=)
c.651C= (p.Gly217=)
19g.44908869C>GCA507947378APOEc.573C>G (p.Gly191=)
c.651C>G (p.Gly217=)
19g.44908869C>TCA507947379APOEc.573C>T (p.Gly191=)
c.651C>T (p.Gly217=)
dbSNP
19g.44908870C>ACA406304284APOEc.574C>A (p.Leu192Ile)
c.652C>A (p.Leu218Ile)
19g.44908870C=CA2338167935APOEc.574C= (p.Leu192=)
c.652C= (p.Leu218=)
19g.44908870C>GCA406304285APOEc.574C>G (p.Leu192Val)
c.652C>G (p.Leu218Val)
dbSNP
19g.44908870C>TCA406304286APOEc.574C>T (p.Leu192Phe)
c.652C>T (p.Leu218Phe)
19g.44908871T>ACA406304287APOEc.575T>A (p.Leu192His)
c.653T>A (p.Leu218His)
19g.44908871T>CCA406304288APOEc.575T>C (p.Leu192Pro)
c.653T>C (p.Leu218Pro)
19g.44908871T>GCA406304289APOEc.575T>G (p.Leu192Arg)
c.653T>G (p.Leu218Arg)

Number of alleles fetched