Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908753_44908776dupCA2582192292APOEc.457_480dup (p.Arg160_Lys161insValArgLeuAlaSerHisLeuArg)
c.535_558dup (p.Arg186_Lys187insValArgLeuAlaSerHisLeuArg)
gnomAD v3 gnomAD v4
19g.44908765T>ACA308885728APOEc.469T>A (p.Ser157Thr)
c.547T>A (p.Ser183Thr)
dbSNP gnomAD v4
19g.44908765T>CCA406304077APOEc.469T>C (p.Ser157Pro)
c.547T>C (p.Ser183Pro)
gnomAD v4
19g.44908765T>GCA406304078APOEc.469T>G (p.Ser157Ala)
c.547T>G (p.Ser183Ala)
gnomAD v4
19g.44908765T=CA2338167729APOEc.469T= (p.Ser157=)
c.547T= (p.Ser183=)
19g.44908766C>ACA406304079APOEc.470C>A (p.Ser157Tyr)
c.548C>A (p.Ser183Tyr)
gnomAD v4
19g.44908766C=CA2338167731APOEc.470C= (p.Ser157=)
c.548C= (p.Ser183=)
19g.44908766C>GCA406304080APOEc.470C>G (p.Ser157Cys)
c.548C>G (p.Ser183Cys)
dbSNP
19g.44908766C>TCA406304081APOEc.470C>T (p.Ser157Phe)
c.548C>T (p.Ser183Phe)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908768delCA2585715440APOEc.472del (p.His158ThrfsTer?)
c.550del (p.His184ThrfsTer?)
gnomAD v4
19g.44908767_44908771delCA2585715441APOEc.471_475del (p.His158AlafsTer5)
c.549_553del (p.His184AlafsTer5)
gnomAD v4
19g.44908767C>ACA507947727APOEc.471C>A (p.Ser157=)
c.549C>A (p.Ser183=)
dbSNP gnomAD v4
19g.44908767C=CA2338167734APOEc.471C= (p.Ser157=)
c.549C= (p.Ser183=)
19g.44908767C>GCA507947729APOEc.471C>G (p.Ser157=)
c.549C>G (p.Ser183=)
19g.44908767C>TCA507947728APOEc.471C>T (p.Ser157=)
c.549C>T (p.Ser183=)
gnomAD v4
19g.44908768C>ACA308885733APOEc.472C>A (p.His158Asn)
c.550C>A (p.His184Asn)
dbSNP gnomAD v4
19g.44908768C=CA2338167863APOEc.472C= (p.His158=)
c.550C= (p.His184=)
19g.44908768C>GCA406304082APOEc.472C>G (p.His158Asp)
c.550C>G (p.His184Asp)
19g.44908768C>TCA406304083APOEc.472C>T (p.His158Tyr)
c.550C>T (p.His184Tyr)
dbSNP gnomAD v2 gnomAD v4
19g.44908769A>CCA406304085APOEc.473A>C (p.His158Pro)
c.551A>C (p.His184Pro)
19g.44908769A>GCA406304086APOEc.473A>G (p.His158Arg)
c.551A>G (p.His184Arg)
gnomAD v4
19g.44908769A>TCA406304087APOEc.473A>T (p.His158Leu)
c.551A>T (p.His184Leu)
gnomAD v4
19g.44908770C>ACA406304088APOEc.474C>A (p.His158Gln)
c.552C>A (p.His184Gln)
dbSNP gnomAD v3 gnomAD v4
19g.44908770C=CA2338167864APOEc.474C= (p.His158=)
c.552C= (p.His184=)
19g.44908770C>GCA406304089APOEc.474C>G (p.His158Gln)
c.552C>G (p.His184Gln)
gnomAD v4
19g.44908770C>TCA507947743APOEc.474C>T (p.His158=)
c.552C>T (p.His184=)
dbSNP gnomAD v4
19g.44908771C>ACA308885734APOEc.475C>A (p.Leu159Met)
c.553C>A (p.Leu185Met)
dbSNP gnomAD v4
19g.44908771C=CA2338167865APOEc.475C= (p.Leu159=)
c.553C= (p.Leu185=)
19g.44908771C>GCA406304090APOEc.475C>G (p.Leu159Val)
c.553C>G (p.Leu185Val)
19g.44908771C>TCA507947746APOEc.475C>T (p.Leu159=)
c.553C>T (p.Leu185=)
dbSNP gnomAD v2 gnomAD v4
19g.44908776_44908784delCA2580097378APOEc.480_488del (p.Lys161_Arg163del)
c.558_566del (p.Lys187_Arg189del)
ClinVar
19g.44908772T>ACA406304091APOEc.476T>A (p.Leu159Gln)
c.554T>A (p.Leu185Gln)
gnomAD v4
19g.44908772T>CCA406304092APOEc.476T>C (p.Leu159Pro)
c.554T>C (p.Leu185Pro)
dbSNP gnomAD v2 gnomAD v4
19g.44908772T>GCA406304093APOEc.476T>G (p.Leu159Arg)
c.554T>G (p.Leu185Arg)
19g.44908772T=CA2338167866APOEc.476T= (p.Leu159=)
c.554T= (p.Leu185=)
19g.44908773G>ACA507947747APOEc.477G>A (p.Leu159=)
c.555G>A (p.Leu185=)
dbSNP gnomAD v2 gnomAD v4
19g.44908773G>CCA507947750APOEc.477G>C (p.Leu159=)
c.555G>C (p.Leu185=)
19g.44908773G=CA2338167867APOEc.477G= (p.Leu159=)
c.555G= (p.Leu185=)
19g.44908773G>TCA507947748APOEc.477G>T (p.Leu159=)
c.555G>T (p.Leu185=)
gnomAD v4
19g.44908773_44908780delCA2585715442APOEc.477_484del (p.Arg160AlafsTer2)
c.555_562del (p.Arg186AlafsTer2)
gnomAD v4
19g.44908776_44908790delCA2695228863APOEc.480_494del (p.Lys161_Arg165del)
c.558_572del (p.Lys187_Arg191del)
19g.44908774C>ACA406304094APOEc.478C>A (p.Arg160Ser)
c.556C>A (p.Arg186Ser)
gnomAD v4
19g.44908774C=CA2338167868APOEc.478C= (p.Arg160=)
c.556C= (p.Arg186=)
19g.44908774C>GCA406304095APOEc.478C>G (p.Arg160Gly)
c.556C>G (p.Arg186Gly)
dbSNP gnomAD v2 gnomAD v4
19g.44908774C>TCA041132APOEc.478C>T (p.Arg160Cys)
c.556C>T (p.Arg186Cys)
ClinVar dbSNP gnomAD v4
19g.44908775G>ACA406304096APOEc.479G>A (p.Arg160His)
c.557G>A (p.Arg186His)
dbSNP gnomAD v2 gnomAD v4
19g.44908775G>CCA406304098APOEc.479G>C (p.Arg160Pro)
c.557G>C (p.Arg186Pro)
19g.44908775G=CA2338167869APOEc.479G= (p.Arg160=)
c.557G= (p.Arg186=)
19g.44908775G>TCA406304097APOEc.479G>T (p.Arg160Leu)
c.557G>T (p.Arg186Leu)
gnomAD v4
19g.44908776C>ACA9506073APOEc.480C>A (p.Arg160=)
c.558C>A (p.Arg186=)
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched