Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908711_44908731dupCA127504APOEc.415_435dup (p.Gly145_Gln146insGluValGlnAlaMetLeuGly)
c.493_513dup (p.Gly171_Gln172insGluValGlnAlaMetLeuGly)
ClinVar dbSNP
19g.44908722C>ACA308885549APOEc.426C>A (p.Ala142=)
c.504C>A (p.Ala168=)
dbSNP
19g.44908722C=CA2338167625APOEc.426C= (p.Ala142=)
c.504C= (p.Ala168=)
19g.44908722C>GCA507947619APOEc.426C>G (p.Ala142=)
c.504C>G (p.Ala168=)
19g.44908722C>TCA507947621APOEc.426C>T (p.Ala142=)
c.504C>T (p.Ala168=)
19g.44908723A=CA2338167629APOEc.427A= (p.Met143=)
c.505A= (p.Met169=)
19g.44908723A>CCA9506064APOEc.427A>C (p.Met143Leu)
c.505A>C (p.Met169Leu)
dbSNP ExAC gnomAD
19g.44908723A>GCA406304004APOEc.427A>G (p.Met143Val)
c.505A>G (p.Met169Val)
19g.44908723A>TCA9506063APOEc.427A>T (p.Met143Leu)
c.505A>T (p.Met169Leu)
dbSNP ExAC gnomAD
19g.44908724T>ACA406304005APOEc.428T>A (p.Met143Lys)
c.506T>A (p.Met169Lys)
19g.44908724T>CCA406304006APOEc.428T>C (p.Met143Thr)
c.506T>C (p.Met169Thr)
19g.44908724T>GCA406304007APOEc.428T>G (p.Met143Arg)
c.506T>G (p.Met169Arg)
19g.44908725G>ACA406304008APOEc.429G>A (p.Met143Ile)
c.507G>A (p.Met169Ile)
COSMIC
19g.44908725G>CCA406304009APOEc.429G>C (p.Met143Ile)
c.507G>C (p.Met169Ile)
19g.44908725G>TCA406304010APOEc.429G>T (p.Met143Ile)
c.507G>T (p.Met169Ile)
19g.44908726C>ACA406304013APOEc.430C>A (p.Leu144Ile)
c.508C>A (p.Leu170Ile)
gnomAD
19g.44908726C=CA2338167634APOEc.430C= (p.Leu144=)
c.508C= (p.Leu170=)
19g.44908726C>GCA406304011APOEc.430C>G (p.Leu144Val)
c.508C>G (p.Leu170Val)
19g.44908726C>TCA406304012APOEc.430C>T (p.Leu144Phe)
c.508C>T (p.Leu170Phe)
19g.44908727T>ACA406304014APOEc.431T>A (p.Leu144His)
c.509T>A (p.Leu170His)
19g.44908727T>CCA406304015APOEc.431T>C (p.Leu144Pro)
c.509T>C (p.Leu170Pro)
19g.44908727T>GCA406304016APOEc.431T>G (p.Leu144Arg)
c.509T>G (p.Leu170Arg)
19g.44908728C>ACA507947634APOEc.432C>A (p.Leu144=)
c.510C>A (p.Leu170=)
19g.44908728C=CA2338167640APOEc.432C= (p.Leu144=)
c.510C= (p.Leu170=)
19g.44908728C>GCA507947635APOEc.432C>G (p.Leu144=)
c.510C>G (p.Leu170=)
19g.44908728C>TCA507947637APOEc.432C>T (p.Leu144=)
c.510C>T (p.Leu170=)
gnomAD
19g.44908729G>ACA9506065APOEc.433G>A (p.Gly145Ser)
c.511G>A (p.Gly171Ser)
dbSNP ExAC gnomAD
19g.44908729G>CCA406304017APOEc.433G>C (p.Gly145Arg)
c.511G>C (p.Gly171Arg)
gnomAD
19g.44908729G=CA2338167645APOEc.433G= (p.Gly145=)
c.511G= (p.Gly171=)
19g.44908729G>TCA308885595APOEc.433G>T (p.Gly145Cys)
c.511G>T (p.Gly171Cys)
dbSNP
19g.44908730G>ACA041273APOEc.434G>A (p.Gly145Asp)
c.512G>A (p.Gly171Asp)
ClinVar dbSNP ExAC gnomAD
19g.[44908730G>A;44908822C>T]CA041311APOEc.[434G>A;526C>T] (p.[Gly145Asp;Arg176Cys])
c.[512G>A;604C>T] (p.[Gly171Asp;Arg202Cys])
ClinVar
19g.44908730G>CCA406304018APOEc.434G>C (p.Gly145Ala)
c.512G>C (p.Gly171Ala)
gnomAD
19g.44908730G=CA2338167652APOEc.434G= (p.Gly145=)
c.512G= (p.Gly171=)
19g.44908730G>TCA406304019APOEc.434G>T (p.Gly145Val)
c.512G>T (p.Gly171Val)
19g.44908731C>ACA507947643APOEc.435C>A (p.Gly145=)
c.513C>A (p.Gly171=)
19g.44908731C=CA2338167657APOEc.435C= (p.Gly145=)
c.513C= (p.Gly171=)
19g.44908731C>GCA507947646APOEc.435C>G (p.Gly145=)
c.513C>G (p.Gly171=)
gnomAD
19g.44908731C>TCA507947644APOEc.435C>T (p.Gly145=)
c.513C>T (p.Gly171=)
gnomAD
19g.44908732C>ACA406304020APOEc.436C>A (p.Gln146Lys)
c.514C>A (p.Gln172Lys)
19g.44908732C=CA2338167659APOEc.436C= (p.Gln146=)
c.514C= (p.Gln172=)
19g.44908732C>GCA406304021APOEc.436C>G (p.Gln146Glu)
c.514C>G (p.Gln172Glu)
19g.44908732C>TCA406304022APOEc.436C>T (p.Gln146Ter)
c.514C>T (p.Gln172Ter)
gnomAD
19g.44908733A=CA2338167661APOEc.437A= (p.Gln146=)
c.515A= (p.Gln172=)
19g.44908733A>CCA406304023APOEc.437A>C (p.Gln146Pro)
c.515A>C (p.Gln172Pro)
19g.44908733A>GCA406304025APOEc.437A>G (p.Gln146Arg)
c.515A>G (p.Gln172Arg)
19g.44908733A>TCA406304024APOEc.437A>T (p.Gln146Leu)
c.515A>T (p.Gln172Leu)
19g.44908734G>ACA507947653APOEc.438G>A (p.Gln146=)
c.516G>A (p.Gln172=)
19g.44908734G>CCA406304026APOEc.438G>C (p.Gln146His)
c.516G>C (p.Gln172His)
19g.44908734G>TCA406304027APOEc.438G>T (p.Gln146His)
c.516G>T (p.Gln172His)

Number of alleles fetched