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.44908757G>ACA406304067APOEc.461G>A (p.Arg154His)
c.539G>A (p.Arg180His)
dbSNP gnomAD v3 gnomAD v4
19g.44908757G>CCA308885705APOEc.461G>C (p.Arg154Pro)
c.539G>C (p.Arg180Pro)
dbSNP
19g.44908757G=CA2338167723APOEc.461G= (p.Arg154=)
c.539G= (p.Arg180=)
19g.44908757G>TCA16044403APOEc.461G>T (p.Arg154Leu)
c.539G>T (p.Arg180Leu)
ClinVar dbSNP gnomAD v4
19g.44908758C>ACA507947712APOEc.462C>A (p.Arg154=)
c.540C>A (p.Arg180=)
19g.44908758C=CA2338167724APOEc.462C= (p.Arg154=)
c.540C= (p.Arg180=)
19g.44908758C>GCA507947714APOEc.462C>G (p.Arg154=)
c.540C>G (p.Arg180=)
dbSNP
19g.44908758C>TCA9506072APOEc.462C>T (p.Arg154=)
c.540C>T (p.Arg180=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908759C>ACA406304069APOEc.463C>A (p.Leu155Ile)
c.541C>A (p.Leu181Ile)
gnomAD v4
19g.44908759C=CA2338167725APOEc.463C= (p.Leu155=)
c.541C= (p.Leu181=)
19g.44908759C>GCA308885718APOEc.463C>G (p.Leu155Val)
c.541C>G (p.Leu181Val)
dbSNP gnomAD v4
19g.44908759C>TCA406304068APOEc.463C>T (p.Leu155Phe)
c.541C>T (p.Leu181Phe)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908760T>ACA406304072APOEc.464T>A (p.Leu155His)
c.542T>A (p.Leu181His)
19g.44908760T>CCA406304070APOEc.464T>C (p.Leu155Pro)
c.542T>C (p.Leu181Pro)
gnomAD v4
19g.44908760T>GCA406304071APOEc.464T>G (p.Leu155Arg)
c.542T>G (p.Leu181Arg)
19g.44908761C>ACA507947717APOEc.465C>A (p.Leu155=)
c.543C>A (p.Leu181=)
gnomAD v4
19g.44908761C=CA2338167726APOEc.465C= (p.Leu155=)
c.543C= (p.Leu181=)
19g.44908761C>GCA507947716APOEc.465C>G (p.Leu155=)
c.543C>G (p.Leu181=)
19g.44908761C>TCA507947715APOEc.465C>T (p.Leu155=)
c.543C>T (p.Leu181=)
dbSNP gnomAD v2 gnomAD v4
19g.44908762G>ACA308885721APOEc.466G>A (p.Ala156Thr)
c.544G>A (p.Ala182Thr)
dbSNP gnomAD v2 gnomAD v4
19g.44908762G>CCA406304073APOEc.466G>C (p.Ala156Pro)
c.544G>C (p.Ala182Pro)
gnomAD v4
19g.44908762G=CA2338167727APOEc.466G= (p.Ala156=)
c.544G= (p.Ala182=)
19g.44908762G>TCA308885722APOEc.466G>T (p.Ala156Ser)
c.544G>T (p.Ala182Ser)
dbSNP gnomAD v3 gnomAD v4
19g.44908763C>ACA406304076APOEc.467C>A (p.Ala156Asp)
c.545C>A (p.Ala182Asp)
gnomAD v4
19g.44908763C>GCA406304075APOEc.467C>G (p.Ala156Gly)
c.545C>G (p.Ala182Gly)
19g.44908763C>TCA406304074APOEc.467C>T (p.Ala156Val)
c.545C>T (p.Ala182Val)
gnomAD v4
19g.44908764C>ACA507947719APOEc.468C>A (p.Ala156=)
c.546C>A (p.Ala182=)
gnomAD v4
19g.44908764C=CA2338167728APOEc.468C= (p.Ala156=)
c.546C= (p.Ala182=)
19g.44908764C>GCA507947720APOEc.468C>G (p.Ala156=)
c.546C>G (p.Ala182=)
gnomAD v4
19g.44908764C>TCA507947721APOEc.468C>T (p.Ala156=)
c.546C>T (p.Ala182=)
dbSNP gnomAD v2
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)

Number of alleles fetched