Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908904T>ACA406304372APOEc.608T>A (p.Val203Glu)
c.686T>A (p.Val229Glu)
19g.44908904T>CCA406304373APOEc.608T>C (p.Val203Ala)
c.686T>C (p.Val229Ala)
19g.44908904T>GCA406304370APOEc.608T>G (p.Val203Gly)
c.686T>G (p.Val229Gly)
19g.44908905G>ACA507947432APOEc.609G>A (p.Val203=)
c.687G>A (p.Val229=)
19g.44908905G>CCA507947434APOEc.609G>C (p.Val203=)
c.687G>C (p.Val229=)
19g.44908905G>TCA507947435APOEc.609G>T (p.Val203=)
c.687G>T (p.Val229=)
19g.44908905_44908924delCA2695228869APOEc.609_628del (p.Glu204ArgfsTer?)
c.687_706del (p.Glu230ArgfsTer?)
19g.44908906G>ACA406304377APOEc.610G>A (p.Glu204Lys)
c.688G>A (p.Glu230Lys)
gnomAD v4
19g.44908906G>CCA406304374APOEc.610G>C (p.Glu204Gln)
c.688G>C (p.Glu230Gln)
19g.44908906G>TCA406304375APOEc.610G>T (p.Glu204Ter)
c.688G>T (p.Glu230Ter)
19g.44908907A>CCA406304379APOEc.611A>C (p.Glu204Ala)
c.689A>C (p.Glu230Ala)
19g.44908907A>GCA406304380APOEc.611A>G (p.Glu204Gly)
c.689A>G (p.Glu230Gly)
gnomAD v4
19g.44908907A>TCA406304382APOEc.611A>T (p.Glu204Val)
c.689A>T (p.Glu230Val)
19g.44908908A>CCA406304383APOEc.612A>C (p.Glu204Asp)
c.690A>C (p.Glu230Asp)
19g.44908908A>GCA507947440APOEc.612A>G (p.Glu204=)
c.690A>G (p.Glu230=)
19g.44908908A>TCA406304385APOEc.612A>T (p.Glu204Asp)
c.690A>T (p.Glu230Asp)
19g.44908909C>ACA406304386APOEc.613C>A (p.Gln205Lys)
c.691C>A (p.Gln231Lys)
19g.44908909C>GCA406304388APOEc.613C>G (p.Gln205Glu)
c.691C>G (p.Gln231Glu)
dbSNP gnomAD v3 gnomAD v4
19g.44908909C>TCA406304389APOEc.613C>T (p.Gln205Ter)
c.691C>T (p.Gln231Ter)
gnomAD v4
19g.44908910A=CA2338167955APOEc.614A= (p.Gln205=)
c.692A= (p.Gln231=)
19g.44908910A>CCA406304391APOEc.614A>C (p.Gln205Pro)
c.692A>C (p.Gln231Pro)
19g.44908910A>GCA308885900APOEc.614A>G (p.Gln205Arg)
c.692A>G (p.Gln231Arg)
dbSNP gnomAD v4
19g.44908910A>TCA406304393APOEc.614A>T (p.Gln205Leu)
c.692A>T (p.Gln231Leu)
19g.44908910dupCA2585715452APOEc.614dup (p.Arg207ProfsTer?)
c.692dup (p.Arg233ProfsTer?)
gnomAD v4
19g.44908911G>ACA507947443APOEc.615G>A (p.Gln205=)
c.693G>A (p.Gln231=)
ClinVar
19g.44908911G>CCA406304394APOEc.615G>C (p.Gln205His)
c.693G>C (p.Gln231His)
19g.44908911G=CA2740130017APOEc.615G= (p.Gln205=)
c.693G= (p.Gln231=)
19g.44908911G>TCA406304396APOEc.615G>T (p.Gln205His)
c.693G>T (p.Gln231His)
19g.44908912G>ACA406304397APOEc.616G>A (p.Gly206Ser)
c.694G>A (p.Gly232Ser)
gnomAD v4
19g.44908912G>CCA406304399APOEc.616G>C (p.Gly206Arg)
c.694G>C (p.Gly232Arg)
19g.44908912G>TCA406304401APOEc.616G>T (p.Gly206Cys)
c.694G>T (p.Gly232Cys)
19g.44908913G>ACA406304402APOEc.617G>A (p.Gly206Asp)
c.695G>A (p.Gly232Asp)
dbSNP gnomAD v4
19g.44908913G>CCA406304403APOEc.617G>C (p.Gly206Ala)
c.695G>C (p.Gly232Ala)
19g.44908913G=CA2338167956APOEc.617G= (p.Gly206=)
c.695G= (p.Gly232=)
19g.44908913G>TCA406304405APOEc.617G>T (p.Gly206Val)
c.695G>T (p.Gly232Val)
19g.44908914C>ACA507947446APOEc.618C>A (p.Gly206=)
c.696C>A (p.Gly232=)
dbSNP gnomAD v4
19g.44908914C=CA2338167957APOEc.618C= (p.Gly206=)
c.696C= (p.Gly232=)
19g.44908914C>GCA507947447APOEc.618C>G (p.Gly206=)
c.696C>G (p.Gly232=)
19g.44908914C>TCA507947445APOEc.618C>T (p.Gly206=)
c.696C>T (p.Gly232=)
gnomAD v4
19g.44908915C>ACA406304406APOEc.619C>A (p.Arg207Ser)
c.697C>A (p.Arg233Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908915C=CA2338167958APOEc.619C= (p.Arg207=)
c.697C= (p.Arg233=)
19g.44908915C>GCA406304408APOEc.619C>G (p.Arg207Gly)
c.697C>G (p.Arg233Gly)
dbSNP gnomAD v3 gnomAD v4
19g.44908915C>TCA9506082APOEc.619C>T (p.Arg207Cys)
c.697C>T (p.Arg233Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908916G>ACA406304410APOEc.620G>A (p.Arg207His)
c.698G>A (p.Arg233His)
dbSNP gnomAD v2 gnomAD v4
19g.44908916G>CCA406304411APOEc.620G>C (p.Arg207Pro)
c.698G>C (p.Arg233Pro)
dbSNP gnomAD v2 gnomAD v4
19g.44908916G=CA2338167959APOEc.620G= (p.Arg207=)
c.698G= (p.Arg233=)
19g.44908916G>TCA406304413APOEc.620G>T (p.Arg207Leu)
c.698G>T (p.Arg233Leu)
19g.44908917C>ACA507947449APOEc.621C>A (p.Arg207=)
c.699C>A (p.Arg233=)
ClinVar gnomAD v4
19g.44908917C=CA2338167960APOEc.621C= (p.Arg207=)
c.699C= (p.Arg233=)
19g.44908917C>GCA507947451APOEc.621C>G (p.Arg207=)
c.699C>G (p.Arg233=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.44908917C>TCA507947453APOEc.621C>T (p.Arg207=)
c.699C>T (p.Arg233=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.44908918G>ACA308885904APOEc.622G>A (p.Val208Met)
c.700G>A (p.Val234Met)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908918G>CCA9506083APOEc.622G>C (p.Val208Leu)
c.700G>C (p.Val234Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908918G=CA2338167961APOEc.622G= (p.Val208=)
c.700G= (p.Val234=)
19g.44908918G>TCA406304415APOEc.622G>T (p.Val208Leu)
c.700G>T (p.Val234Leu)
19g.44908919T>ACA406304417APOEc.623T>A (p.Val208Glu)
c.701T>A (p.Val234Glu)
19g.44908919T>CCA406304418APOEc.623T>C (p.Val208Ala)
c.701T>C (p.Val234Ala)
19g.44908919T>GCA406304420APOEc.623T>G (p.Val208Gly)
c.701T>G (p.Val234Gly)
ClinVar
19g.44908919T=CA2740130018APOEc.623T= (p.Val208=)
c.701T= (p.Val234=)
19g.44908920G>ACA507947461APOEc.624G>A (p.Val208=)
c.702G>A (p.Val234=)
19g.44908920G>CCA507947462APOEc.624G>C (p.Val208=)
c.702G>C (p.Val234=)
19g.44908920G>TCA507947463APOEc.624G>T (p.Val208=)
c.702G>T (p.Val234=)
19g.44908921C>ACA507947464APOEc.625C>A (p.Arg209=)
c.703C>A (p.Arg235=)
19g.44908921C=CA2338167962APOEc.625C= (p.Arg209=)
c.703C= (p.Arg235=)
19g.44908921C>GCA406304421APOEc.625C>G (p.Arg209Gly)
c.703C>G (p.Arg235Gly)
19g.44908921C>TCA406304422APOEc.625C>T (p.Arg209Trp)
c.703C>T (p.Arg235Trp)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.44908922G>ACA308885916APOEc.626G>A (p.Arg209Gln)
c.704G>A (p.Arg235Gln)
dbSNP gnomAD v3 gnomAD v4
19g.44908922G>CCA406304424APOEc.626G>C (p.Arg209Pro)
c.704G>C (p.Arg235Pro)
dbSNP
19g.44908922G=CA2338167963APOEc.626G= (p.Arg209=)
c.704G= (p.Arg235=)
19g.44908922G>TCA406304425APOEc.626G>T (p.Arg209Leu)
c.704G>T (p.Arg235Leu)
gnomAD v4
19g.44908924delCA2585715453APOEc.628del (p.Ala210ProfsTer?)
c.706del (p.Ala236ProfsTer?)
gnomAD v4
19g.44908923G>ACA9506084APOEc.627G>A (p.Arg209=)
c.705G>A (p.Arg235=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908923G>CCA507947467APOEc.627G>C (p.Arg209=)
c.705G>C (p.Arg235=)
19g.44908923G=CA2338167964APOEc.627G= (p.Arg209=)
c.705G= (p.Arg235=)
19g.44908923G>TCA507947469APOEc.627G>T (p.Arg209=)
c.705G>T (p.Arg235=)
gnomAD v4
19g.44908924G>ACA406304428APOEc.628G>A (p.Ala210Thr)
c.706G>A (p.Ala236Thr)
gnomAD v4
19g.44908924G>CCA406304432APOEc.628G>C (p.Ala210Pro)
c.706G>C (p.Ala236Pro)
19g.44908924G>TCA406304433APOEc.628G>T (p.Ala210Ser)
c.706G>T (p.Ala236Ser)
gnomAD v4
19g.44908925C>ACA406304437APOEc.629C>A (p.Ala210Asp)
c.707C>A (p.Ala236Asp)
19g.44908925C>GCA406304438APOEc.629C>G (p.Ala210Gly)
c.707C>G (p.Ala236Gly)
19g.44908925C>TCA406304435APOEc.629C>T (p.Ala210Val)
c.707C>T (p.Ala236Val)
19g.44908926C>ACA507947472APOEc.630C>A (p.Ala210=)
c.708C>A (p.Ala236=)
19g.44908926C=CA2338167965APOEc.630C= (p.Ala210=)
c.708C= (p.Ala236=)
19g.44908926C>GCA507947473APOEc.630C>G (p.Ala210=)
c.708C>G (p.Ala236=)
19g.44908926C>TCA507947474APOEc.630C>T (p.Ala210=)
c.708C>T (p.Ala236=)
dbSNP gnomAD v2 gnomAD v4
19g.44908927G>ACA406304440APOEc.631G>A (p.Ala211Thr)
c.709G>A (p.Ala237Thr)
dbSNP gnomAD v2 gnomAD v4
19g.44908927G>CCA406304441APOEc.631G>C (p.Ala211Pro)
c.709G>C (p.Ala237Pro)
19g.44908927G=CA2338167966APOEc.631G= (p.Ala211=)
c.709G= (p.Ala237=)
19g.44908927G>TCA406304442APOEc.631G>T (p.Ala211Ser)
c.709G>T (p.Ala237Ser)
gnomAD v4
19g.44908928C>ACA406304444APOEc.632C>A (p.Ala211Asp)
c.710C>A (p.Ala237Asp)
19g.44908928C>GCA406304445APOEc.632C>G (p.Ala211Gly)
c.710C>G (p.Ala237Gly)
19g.44908928C>TCA406304447APOEc.632C>T (p.Ala211Val)
c.710C>T (p.Ala237Val)
19g.44908929C>ACA507947477APOEc.633C>A (p.Ala211=)
c.711C>A (p.Ala237=)
19g.44908929C>GCA507947480APOEc.633C>G (p.Ala211=)
c.711C>G (p.Ala237=)
19g.44908929C>TCA507947476APOEc.633C>T (p.Ala211=)
c.711C>T (p.Ala237=)
19g.44908930A>CCA406304451APOEc.634A>C (p.Thr212Pro)
c.712A>C (p.Thr238Pro)
19g.44908930A>GCA406304448APOEc.634A>G (p.Thr212Ala)
c.712A>G (p.Thr238Ala)
gnomAD v4
19g.44908930A>TCA406304449APOEc.634A>T (p.Thr212Ser)
c.712A>T (p.Thr238Ser)
19g.44908931C>ACA406304452APOEc.635C>A (p.Thr212Asn)
c.713C>A (p.Thr238Asn)
19g.44908931C>GCA406304454APOEc.635C>G (p.Thr212Ser)
c.713C>G (p.Thr238Ser)
19g.44908931C>TCA406304455APOEc.635C>T (p.Thr212Ile)
c.713C>T (p.Thr238Ile)
19g.44908931_44908934delCA2695228870APOEc.635_638del (p.Thr212ArgfsTer?)
c.713_716del (p.Thr238ArgfsTer?)
19g.44908932_44908941delCA2580612068APOEc.636_645del (p.Val213TrpfsTer?)
c.714_723del (p.Val239TrpfsTer?)
c.636_645del (p.Thr212=)
19g.44908932T>ACA507947488APOEc.636T>A (p.Thr212=)
c.714T>A (p.Thr238=)
19g.44908932T>CCA507947485APOEc.636T>C (p.Thr212=)
c.714T>C (p.Thr238=)
gnomAD v4
19g.44908932T>GCA507947486APOEc.636T>G (p.Thr212=)
c.714T>G (p.Thr238=)
19g.44908933G>ACA406304457APOEc.637G>A (p.Val213Met)
c.715G>A (p.Val239Met)
19g.44908933G>CCA406304458APOEc.637G>C (p.Val213Leu)
c.715G>C (p.Val239Leu)
19g.44908933G>TCA406304460APOEc.637G>T (p.Val213Leu)
c.715G>T (p.Val239Leu)
19g.44908934T>ACA406304465APOEc.638T>A (p.Val213Glu)
c.716T>A (p.Val239Glu)
19g.44908934T>CCA406304464APOEc.638T>C (p.Val213Ala)
c.716T>C (p.Val239Ala)
19g.44908934T>GCA406304462APOEc.638T>G (p.Val213Gly)
c.716T>G (p.Val239Gly)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908934T=CA2338167967APOEc.638T= (p.Val213=)
c.716T= (p.Val239=)
19g.44908935G>ACA507947492APOEc.639G>A (p.Val213=)
c.717G>A (p.Val239=)
19g.44908935G>CCA507947496APOEc.639G>C (p.Val213=)
c.717G>C (p.Val239=)
19g.44908935G=CA2338167968APOEc.639G= (p.Val213=)
c.717G= (p.Val239=)
19g.44908935G>TCA507947491APOEc.639G>T (p.Val213=)
c.717G>T (p.Val239=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908936G>ACA9506085APOEc.640G>A (p.Gly214Ser)
c.718G>A (p.Gly240Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908936G>CCA406304467APOEc.640G>C (p.Gly214Arg)
c.718G>C (p.Gly240Arg)
19g.44908936G=CA2338167969APOEc.640G= (p.Gly214=)
c.718G= (p.Gly240=)
19g.44908936G>TCA406304469APOEc.640G>T (p.Gly214Cys)
c.718G>T (p.Gly240Cys)
dbSNP
19g.44908937G>ACA406304471APOEc.641G>A (p.Gly214Asp)
c.719G>A (p.Gly240Asp)
gnomAD v4
19g.44908937G>CCA406304472APOEc.641G>C (p.Gly214Ala)
c.719G>C (p.Gly240Ala)
19g.44908937G>TCA406304474APOEc.641G>T (p.Gly214Val)
c.719G>T (p.Gly240Val)
19g.44908938C>ACA507947502APOEc.642C>A (p.Gly214=)
c.720C>A (p.Gly240=)
gnomAD v4
19g.44908938C=CA2338167970APOEc.642C= (p.Gly214=)
c.720C= (p.Gly240=)
19g.44908938C>GCA507947501APOEc.642C>G (p.Gly214=)
c.720C>G (p.Gly240=)
19g.44908938C>TCA507947500APOEc.642C>T (p.Gly214=)
c.720C>T (p.Gly240=)
ClinVar dbSNP
19g.44908939T>ACA406304475APOEc.643T>A (p.Ser215Thr)
c.721T>A (p.Ser241Thr)
gnomAD v4
19g.44908939T>CCA406304476APOEc.643T>C (p.Ser215Pro)
c.721T>C (p.Ser241Pro)
dbSNP
19g.44908939T>GCA406304478APOEc.643T>G (p.Ser215Ala)
c.721T>G (p.Ser241Ala)
19g.44908940C>ACA406304482APOEc.644C>A (p.Ser215Tyr)
c.722C>A (p.Ser241Tyr)
19g.44908940C=CA2338167971APOEc.644C= (p.Ser215=)
c.722C= (p.Ser241=)
19g.44908940C>GCA406304479APOEc.644C>G (p.Ser215Cys)
c.722C>G (p.Ser241Cys)
19g.44908940C>TCA308885927APOEc.644C>T (p.Ser215Phe)
c.722C>T (p.Ser241Phe)
dbSNP gnomAD v3 gnomAD v4
19g.44908941C>ACA507947509APOEc.645C>A (p.Ser215=)
c.723C>A (p.Ser241=)
19g.44908941C=CA2338167972APOEc.645C= (p.Ser215=)
c.723C= (p.Ser241=)
19g.44908941C>GCA507947507APOEc.645C>G (p.Ser215=)
c.723C>G (p.Ser241=)
dbSNP
19g.44908941C>TCA507947508APOEc.645C>T (p.Ser215=)
c.723C>T (p.Ser241=)
dbSNP gnomAD v4
19g.44908942C>ACA406304483APOEc.646C>A (p.Leu216Met)
c.724C>A (p.Leu242Met)
19g.44908942C=CA2338167973APOEc.646C= (p.Leu216=)
c.724C= (p.Leu242=)
19g.44908942C>GCA406304485APOEc.646C>G (p.Leu216Val)
c.724C>G (p.Leu242Val)
19g.44908942C>TCA507947513APOEc.646C>T (p.Leu216=)
c.724C>T (p.Leu242=)
dbSNP gnomAD v2 gnomAD v4
19g.44908943T>ACA406304487APOEc.647T>A (p.Leu216Gln)
c.725T>A (p.Leu242Gln)
19g.44908943T>CCA406304488APOEc.647T>C (p.Leu216Pro)
c.725T>C (p.Leu242Pro)
gnomAD v4
19g.44908943T>GCA406304489APOEc.647T>G (p.Leu216Arg)
c.725T>G (p.Leu242Arg)
19g.44908944G>ACA507947514APOEc.648G>A (p.Leu216=)
c.726G>A (p.Leu242=)
19g.44908944G>CCA507947516APOEc.648G>C (p.Leu216=)
c.726G>C (p.Leu242=)
19g.44908944G>TCA507947519APOEc.648G>T (p.Leu216=)
c.726G>T (p.Leu242=)
19g.44908945G>ACA406304495APOEc.649G>A (p.Ala217Thr)
c.727G>A (p.Ala243Thr)
gnomAD v4
19g.44908945G>CCA406304491APOEc.649G>C (p.Ala217Pro)
c.727G>C (p.Ala243Pro)
19g.44908945G>TCA406304493APOEc.649G>T (p.Ala217Ser)
c.727G>T (p.Ala243Ser)
gnomAD v4
19g.44908946C>ACA406304496APOEc.650C>A (p.Ala217Asp)
c.728C>A (p.Ala243Asp)
19g.44908946C>GCA406304497APOEc.650C>G (p.Ala217Gly)
c.728C>G (p.Ala243Gly)
19g.44908946C>TCA406304499APOEc.650C>T (p.Ala217Val)
c.728C>T (p.Ala243Val)
19g.44908947C>ACA507947523APOEc.651C>A (p.Ala217=)
c.729C>A (p.Ala243=)
dbSNP gnomAD v3 gnomAD v4
19g.44908947C=CA2338167974APOEc.651C= (p.Ala217=)
c.729C= (p.Ala243=)
19g.44908947C>GCA507947524APOEc.651C>G (p.Ala217=)
c.729C>G (p.Ala243=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908947C>TCA9506086APOEc.651C>T (p.Ala217=)
c.729C>T (p.Ala243=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908947_44908963delCA2585715454APOEc.651_667del (p.Gly218AlafsTer?)
c.729_745del (p.Gly244AlafsTer?)
gnomAD v4
19g.44908948G>ACA406304502APOEc.652G>A (p.Gly218Ser)
c.730G>A (p.Gly244Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908948G>CCA406304503APOEc.652G>C (p.Gly218Arg)
c.730G>C (p.Gly244Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908948G=CA2338167975APOEc.652G= (p.Gly218=)
c.730G= (p.Gly244=)
19g.44908948G>TCA406304505APOEc.652G>T (p.Gly218Cys)
c.730G>T (p.Gly244Cys)
dbSNP gnomAD v4
19g.44908949G>ACA406304507APOEc.653G>A (p.Gly218Asp)
c.731G>A (p.Gly244Asp)
dbSNP gnomAD v4
19g.44908949G>CCA406304508APOEc.653G>C (p.Gly218Ala)
c.731G>C (p.Gly244Ala)
19g.44908949G=CA2338167976APOEc.653G= (p.Gly218=)
c.731G= (p.Gly244=)
19g.44908949G>TCA406304510APOEc.653G>T (p.Gly218Val)
c.731G>T (p.Gly244Val)
gnomAD v4
19g.44908950C>ACA507947531APOEc.654C>A (p.Gly218=)
c.732C>A (p.Gly244=)
gnomAD v4
19g.44908950C>GCA507947532APOEc.654C>G (p.Gly218=)
c.732C>G (p.Gly244=)
gnomAD v4
19g.44908950C>TCA507947533APOEc.654C>T (p.Gly218=)
c.732C>T (p.Gly244=)
19g.44908951C>ACA406304511APOEc.655C>A (p.Gln219Lys)
c.733C>A (p.Gln245Lys)
gnomAD v4
19g.44908951C=CA2338167977APOEc.655C= (p.Gln219=)
c.733C= (p.Gln245=)
19g.44908951C>GCA308885934APOEc.655C>G (p.Gln219Glu)
c.733C>G (p.Gln245Glu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908951C>TCA406304513APOEc.655C>T (p.Gln219Ter)
c.733C>T (p.Gln245Ter)
dbSNP gnomAD v2
19g.44908952A>CCA406304515APOEc.656A>C (p.Gln219Pro)
c.734A>C (p.Gln245Pro)
19g.44908952A>GCA406304518APOEc.656A>G (p.Gln219Arg)
c.734A>G (p.Gln245Arg)
gnomAD v4
19g.44908952A>TCA406304517APOEc.656A>T (p.Gln219Leu)
c.734A>T (p.Gln245Leu)
19g.44908953G>ACA507947537APOEc.657G>A (p.Gln219=)
c.735G>A (p.Gln245=)
gnomAD v4
19g.44908953G>CCA406304520APOEc.657G>C (p.Gln219His)
c.735G>C (p.Gln245His)
dbSNP
19g.44908953G=CA2338167978APOEc.657G= (p.Gln219=)
c.735G= (p.Gln245=)
19g.44908953G>TCA406304522APOEc.657G>T (p.Gln219His)
c.735G>T (p.Gln245His)
19g.44908954C>ACA406304523APOEc.658C>A (p.Pro220Thr)
c.658C>A
c.736C>A (p.Pro246Thr)
gnomAD v4
19g.44908954C>GCA406304525APOEc.658C>G (p.Pro220Ala)
c.658C>G
c.736C>G (p.Pro246Ala)
19g.44908954C>TCA406304526APOEc.658C>T (p.Pro220Ser)
c.658C>T
c.736C>T (p.Pro246Ser)
gnomAD v4
19g.44908955C>ACA406304528APOEc.659C>A (p.Pro220Gln)
c.737C>A (p.Pro246Gln)
19g.44908955C=CA2338167979APOEc.659C= (p.Pro220=)
c.737C= (p.Pro246=)
19g.44908955C>GCA406304529APOEc.659C>G (p.Pro220Arg)
c.737C>G (p.Pro246Arg)
19g.44908955C>TCA406304532APOEc.659C>T (p.Pro220Leu)
c.737C>T (p.Pro246Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908956G>ACA507947541APOEc.660G>A (p.Pro220=)
c.738G>A (p.Pro246=)
19g.44908956G>CCA507947543APOEc.660G>C (p.Pro220=)
c.738G>C (p.Pro246=)
dbSNP gnomAD v3 gnomAD v4
19g.44908956G=CA2338167980APOEc.660G= (p.Pro220=)
c.738G= (p.Pro246=)
19g.44908956G>TCA507947540APOEc.660G>T (p.Pro220=)
c.738G>T (p.Pro246=)
19g.44908957C>ACA406304534APOEc.661C>A (p.Leu221Ile)
c.739C>A (p.Leu247Ile)
19g.44908957C=CA2338167981APOEc.661C= (p.Leu221=)
c.739C= (p.Leu247=)
19g.44908957C>GCA406304537APOEc.661C>G (p.Leu221Val)
c.739C>G (p.Leu247Val)
dbSNP gnomAD v4
19g.44908957C>TCA507947545APOEc.661C>T (p.Leu221=)
c.739C>T (p.Leu247=)
dbSNP gnomAD v3 gnomAD v4
19g.44908958T>ACA406304539APOEc.662T>A (p.Leu221Gln)
c.740T>A (p.Leu247Gln)
19g.44908958T>CCA406304541APOEc.662T>C (p.Leu221Pro)
c.740T>C (p.Leu247Pro)
dbSNP gnomAD v2 gnomAD v4
19g.44908958T>GCA406304544APOEc.662T>G (p.Leu221Arg)
c.740T>G (p.Leu247Arg)
19g.44908958T=CA2338167982APOEc.662T= (p.Leu221=)
c.740T= (p.Leu247=)
19g.44908959A>CCA507947550APOEc.663A>C (p.Leu221=)
c.741A>C (p.Leu247=)
19g.44908959A>GCA507947552APOEc.663A>G (p.Leu221=)
c.741A>G (p.Leu247=)
dbSNP
19g.44908959A>TCA507947554APOEc.663A>T (p.Leu221=)
c.741A>T (p.Leu247=)
19g.44908960C>ACA406304547APOEc.664C>A (p.Gln222Lys)
c.742C>A (p.Gln248Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908960C=CA2338167983APOEc.664C= (p.Gln222=)
c.742C= (p.Gln248=)
19g.44908960C>GCA406304552APOEc.664C>G (p.Gln222Glu)
c.742C>G (p.Gln248Glu)
gnomAD v4
19g.44908960C>TCA406304550APOEc.664C>T (p.Gln222Ter)
c.742C>T (p.Gln248Ter)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908961A=CA2338167984APOEc.665A= (p.Gln222=)
c.743A= (p.Gln248=)
19g.44908961A>CCA406304554APOEc.665A>C (p.Gln222Pro)
c.743A>C (p.Gln248Pro)
dbSNP gnomAD v4
19g.44908961A>GCA406304555APOEc.665A>G (p.Gln222Arg)
c.743A>G (p.Gln248Arg)
dbSNP gnomAD v2 gnomAD v4
19g.44908961A>TCA308885935APOEc.665A>T (p.Gln222Leu)
c.743A>T (p.Gln248Leu)
dbSNP
19g.44908962G>ACA507947559APOEc.666G>A (p.Gln222=)
c.744G>A (p.Gln248=)
19g.44908962G>CCA406304561APOEc.666G>C (p.Gln222His)
c.744G>C (p.Gln248His)
19g.44908962G>TCA406304563APOEc.666G>T (p.Gln222His)
c.744G>T (p.Gln248His)
19g.44908963G>ACA406304566APOEc.667G>A (p.Glu223Lys)
c.745G>A (p.Glu249Lys)
19g.44908963G>CCA406304568APOEc.667G>C (p.Glu223Gln)
c.745G>C (p.Glu249Gln)
19g.44908963G>TCA406304570APOEc.667G>T (p.Glu223Ter)
c.745G>T (p.Glu249Ter)
gnomAD v4
19g.44908964A>CCA406304572APOEc.668A>C (p.Glu223Ala)
c.746A>C (p.Glu249Ala)
19g.44908964A>GCA406304575APOEc.668A>G (p.Glu223Gly)
c.746A>G (p.Glu249Gly)
19g.44908964A>TCA406304577APOEc.668A>T (p.Glu223Val)
c.746A>T (p.Glu249Val)
19g.44908965G>ACA507947564APOEc.669G>A (p.Glu223=)
c.747G>A (p.Glu249=)
19g.44908965G>CCA406304581APOEc.669G>C (p.Glu223Asp)
c.747G>C (p.Glu249Asp)
19g.44908965G>TCA406304582APOEc.669G>T (p.Glu223Asp)
c.747G>T (p.Glu249Asp)
gnomAD v4
19g.44908966C>ACA507947565APOEc.670C>A (p.Arg224=)
c.748C>A (p.Arg250=)
19g.44908966C>GCA406304585APOEc.670C>G (p.Arg224Gly)
c.748C>G (p.Arg250Gly)
19g.44908966C>TCA406304586APOEc.670C>T (p.Arg224Trp)
c.748C>T (p.Arg250Trp)
ClinVar gnomAD v4
19g.44908967G>ACA406304587APOEc.671G>A (p.Arg224Gln)
c.749G>A (p.Arg250Gln)
gnomAD v4
19g.44908967G>CCA406304589APOEc.671G>C (p.Arg224Pro)
c.749G>C (p.Arg250Pro)
dbSNP gnomAD v2 gnomAD v4
19g.44908967G=CA2338167985APOEc.671G= (p.Arg224=)
c.749G= (p.Arg250=)
19g.44908967G>TCA406304592APOEc.671G>T (p.Arg224Leu)
c.749G>T (p.Arg250Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908968G>ACA507947569APOEc.672G>A (p.Arg224=)
c.750G>A (p.Arg250=)
19g.44908968G>CCA507947570APOEc.672G>C (p.Arg224=)
c.750G>C (p.Arg250=)
19g.44908968G=CA2740130019APOEc.672G= (p.Arg224=)
c.750G= (p.Arg250=)
19g.44908968G>TCA507947571APOEc.672G>T (p.Arg224=)
c.750G>T (p.Arg250=)
ClinVar gnomAD v4
19g.44908969G>ACA308885936APOEc.673G>A (p.Ala225Thr)
c.751G>A (p.Ala251Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908969G>CCA406304595APOEc.673G>C (p.Ala225Pro)
c.751G>C (p.Ala251Pro)
19g.44908969G=CA2338167986APOEc.673G= (p.Ala225=)
c.751G= (p.Ala251=)
19g.44908969G>TCA406304597APOEc.673G>T (p.Ala225Ser)
c.751G>T (p.Ala251Ser)
gnomAD v4
19g.44908970C>ACA406304600APOEc.674C>A (p.Ala225Asp)
c.752C>A (p.Ala251Asp)
gnomAD v4
19g.44908970C>GCA406304606APOEc.674C>G (p.Ala225Gly)
c.752C>G (p.Ala251Gly)
19g.44908970C>TCA406304609APOEc.674C>T (p.Ala225Val)
c.752C>T (p.Ala251Val)
gnomAD v4
19g.44908971C>ACA507947576APOEc.675C>A (p.Ala225=)
c.753C>A (p.Ala251=)
19g.44908971C>GCA507947577APOEc.675C>G (p.Ala225=)
c.753C>G (p.Ala251=)
19g.44908971C>TCA507947578APOEc.675C>T (p.Ala225=)
c.753C>T (p.Ala251=)
gnomAD v4
19g.44908972C>ACA406304613APOEc.676C>A (p.Gln226Lys)
c.754C>A (p.Gln252Lys)
gnomAD v4
19g.44908972C>GCA406304615APOEc.676C>G (p.Gln226Glu)
c.754C>G (p.Gln252Glu)
19g.44908972C>TCA406304617APOEc.676C>T (p.Gln226Ter)
c.754C>T (p.Gln252Ter)
gnomAD v4
19g.44908973A>CCA406304624APOEc.677A>C (p.Gln226Pro)
c.755A>C (p.Gln252Pro)
19g.44908973A>GCA406304621APOEc.677A>G (p.Gln226Arg)
c.755A>G (p.Gln252Arg)
gnomAD v4
19g.44908973A>TCA406304622APOEc.677A>T (p.Gln226Leu)
c.755A>T (p.Gln252Leu)
19g.44908974G>ACA507947583APOEc.678G>A (p.Gln226=)
c.756G>A (p.Gln252=)
19g.44908974G>CCA406304625APOEc.678G>C (p.Gln226His)
c.756G>C (p.Gln252His)
19g.44908974G>TCA406304626APOEc.678G>T (p.Gln226His)
c.756G>T (p.Gln252His)
gnomAD v4
19g.44908975G>ACA406304629APOEc.679G>A (p.Ala227Thr)
c.757G>A (p.Ala253Thr)
gnomAD v4 COSMIC
19g.44908975G>CCA406304631APOEc.679G>C (p.Ala227Pro)
c.757G>C (p.Ala253Pro)
19g.44908975G=CA2338167988APOEc.679G= (p.Ala227=)
c.757G= (p.Ala253=)
19g.44908975G>TCA406304634APOEc.679G>T (p.Ala227Ser)
c.757G>T (p.Ala253Ser)
dbSNP gnomAD v2 gnomAD v4
19g.44908975_44908976delinsGCCA2338167987APOEc.679_680delinsGC (p.Ala227=)
c.757_758delinsGC (p.Ala253=)
19g.44908976C>ACA406304637APOEc.680C>A (p.Ala227Asp)
c.758C>A (p.Ala253Asp)
gnomAD v4
19g.44908976C>GCA406304639APOEc.680C>G (p.Ala227Gly)
c.758C>G (p.Ala253Gly)
19g.44908976C>TCA406304642APOEc.680C>T (p.Ala227Val)
c.758C>T (p.Ala253Val)
19g.44908977delCA882664477APOEc.681del (p.Trp228GlyfsTer23)
c.759del (p.Trp254GlyfsTer?)
c.759del (p.Trp254GlyfsTer23)
dbSNP
19g.44908976_44908985delCA2585715455APOEc.680_689del (p.Ala227GlyfsTer21)
c.758_767del (p.Ala253GlyfsTer?)
c.758_767del (p.Ala253GlyfsTer21)
gnomAD v4
19g.44908977C>ACA507947592APOEc.681C>A (p.Ala227=)
c.759C>A (p.Ala253=)
gnomAD v4
19g.44908977C>GCA507947594APOEc.681C>G (p.Ala227=)
c.759C>G (p.Ala253=)
19g.44908977C>TCA507947595APOEc.681C>T (p.Ala227=)
c.759C>T (p.Ala253=)
19g.44908978T>ACA406304644APOEc.682T>A (p.Trp228Arg)
c.760T>A (p.Trp254Arg)
19g.44908978T>CCA406304646APOEc.682T>C (p.Trp228Arg)
c.760T>C (p.Trp254Arg)
gnomAD v4
19g.44908978T>GCA406304649APOEc.682T>G (p.Trp228Gly)
c.760T>G (p.Trp254Gly)
dbSNP gnomAD v3 gnomAD v4
19g.44908978T=CA2338167989APOEc.682T= (p.Trp228=)
c.760T= (p.Trp254=)
19g.44908979G>ACA127510APOEc.683G>A (p.Trp228Ter)
c.761G>A (p.Trp254Ter)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908979G>CCA406304656APOEc.683G>C (p.Trp228Ser)
c.761G>C (p.Trp254Ser)
19g.44908979G=CA2338167990APOEc.683G= (p.Trp228=)
c.761G= (p.Trp254=)
19g.44908979G>TCA406304652APOEc.683G>T (p.Trp228Leu)
c.761G>T (p.Trp254Leu)
19g.44908982delCA2585715456APOEc.686del (p.Gly229AlafsTer22)
c.764del (p.Gly255AlafsTer?)
c.764del (p.Gly255AlafsTer22)
gnomAD v4
19g.44908980G>ACA406304658APOEc.684G>A (p.Trp228Ter)
c.762G>A (p.Trp254Ter)
19g.44908980G>CCA406304661APOEc.684G>C (p.Trp228Cys)
c.762G>C (p.Trp254Cys)
19g.44908980G>TCA406304664APOEc.684G>T (p.Trp228Cys)
c.762G>T (p.Trp254Cys)
gnomAD v4
19g.44908981G>ACA406304668APOEc.685G>A (p.Gly229Ser)
c.763G>A (p.Gly255Ser)
19g.44908981G>CCA406304670APOEc.685G>C (p.Gly229Arg)
c.763G>C (p.Gly255Arg)
dbSNP gnomAD v2 gnomAD v4
19g.44908981G=CA2338167991APOEc.685G= (p.Gly229=)
c.763G= (p.Gly255=)
19g.44908981G>TCA406304672APOEc.685G>T (p.Gly229Cys)
c.763G>T (p.Gly255Cys)
gnomAD v4
19g.44908982G>ACA406304676APOEc.686G>A (p.Gly229Asp)
c.764G>A (p.Gly255Asp)
gnomAD v4
19g.44908982G>CCA406304679APOEc.686G>C (p.Gly229Ala)
c.764G>C (p.Gly255Ala)
19g.44908982G=CA2338167992APOEc.686G= (p.Gly229=)
c.764G= (p.Gly255=)
19g.44908982G>TCA406304682APOEc.686G>T (p.Gly229Val)
c.764G>T (p.Gly255Val)
dbSNP gnomAD v2 gnomAD v4
19g.44908983C>ACA507947605APOEc.687C>A (p.Gly229=)
c.765C>A (p.Gly255=)
dbSNP gnomAD v2 gnomAD v4
19g.44908983C=CA2338167993APOEc.687C= (p.Gly229=)
c.765C= (p.Gly255=)
19g.44908983C>GCA507947606APOEc.687C>G (p.Gly229=)
c.765C>G (p.Gly255=)
dbSNP
19g.44908983C>TCA507947607APOEc.687C>T (p.Gly229=)
c.765C>T (p.Gly255=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908984G>ACA308885947APOEc.688G>A (p.Glu230Lys)
c.766G>A (p.Glu256Lys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908984G>CCA406304686APOEc.688G>C (p.Glu230Gln)
c.766G>C (p.Glu256Gln)
dbSNP gnomAD v3 gnomAD v4
19g.44908984G=CA2338167994APOEc.688G= (p.Glu230=)
c.766G= (p.Glu256=)
19g.44908984G>TCA406304689APOEc.688G>T (p.Glu230Ter)
c.766G>T (p.Glu256Ter)
gnomAD v4
19g.44908985A>CCA406304695APOEc.689A>C (p.Glu230Ala)
c.767A>C (p.Glu256Ala)
19g.44908985A>GCA406304698APOEc.689A>G (p.Glu230Gly)
c.767A>G (p.Glu256Gly)
19g.44908985A>TCA406304693APOEc.689A>T (p.Glu230Val)
c.767A>T (p.Glu256Val)
19g.44908986G>ACA507947610APOEc.690G>A (p.Glu230=)
c.768G>A (p.Glu256=)
19g.44908986G>CCA406304701APOEc.690G>C (p.Glu230Asp)
c.768G>C (p.Glu256Asp)
19g.44908986G>TCA406304702APOEc.690G>T (p.Glu230Asp)
c.768G>T (p.Glu256Asp)
gnomAD v4
19g.44908987C>ACA507947613APOEc.691C>A (p.Arg231=)
c.769C>A (p.Arg257=)
ClinVar gnomAD v4
19g.44908987C=CA2338167995APOEc.691C= (p.Arg231=)
c.769C= (p.Arg257=)
19g.44908987C>GCA406304705APOEc.691C>G (p.Arg231Gly)
c.769C>G (p.Arg257Gly)
19g.44908987C>TCA406304708APOEc.691C>T (p.Arg231Trp)
c.769C>T (p.Arg257Trp)
dbSNP gnomAD v2 gnomAD v4
19g.44908988G>ACA406304711APOEc.692G>A (p.Arg231Gln)
c.770G>A (p.Arg257Gln)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908988G>CCA406304713APOEc.692G>C (p.Arg231Pro)
c.770G>C (p.Arg257Pro)
19g.44908988G=CA2338167996APOEc.692G= (p.Arg231=)
c.770G= (p.Arg257=)
19g.44908988G>TCA406304716APOEc.692G>T (p.Arg231Leu)
c.770G>T (p.Arg257Leu)
ClinVar gnomAD v4
19g.44908989G>ACA507947620APOEc.693G>A (p.Arg231=)
c.771G>A (p.Arg257=)
gnomAD v4
19g.44908989G>CCA507947618APOEc.693G>C (p.Arg231=)
c.771G>C (p.Arg257=)
19g.44908989G>TCA507947617APOEc.693G>T (p.Arg231=)
c.771G>T (p.Arg257=)
gnomAD v4
19g.44908990C>ACA406304718APOEc.694C>A (p.Leu232Met)
c.772C>A (p.Leu258Met)
gnomAD v4
19g.44908990C>GCA406304721APOEc.694C>G (p.Leu232Val)
c.772C>G (p.Leu258Val)
19g.44908990C>TCA507947626APOEc.694C>T (p.Leu232=)
c.772C>T (p.Leu258=)
gnomAD v4
19g.44908991T>ACA406304723APOEc.695T>A (p.Leu232Gln)
c.773T>A (p.Leu258Gln)
19g.44908991T>CCA406304726APOEc.695T>C (p.Leu232Pro)
c.773T>C (p.Leu258Pro)
19g.44908991T>GCA406304728APOEc.695T>G (p.Leu232Arg)
c.773T>G (p.Leu258Arg)
19g.44908991T=CA2338167997APOEc.695T= (p.Leu232=)
c.773T= (p.Leu258=)
19g.44908992G>ACA507947631APOEc.696G>A (p.Leu232=)
c.774G>A (p.Leu258=)
gnomAD v4
19g.44908992G>CCA507947629APOEc.696G>C (p.Leu232=)
c.774G>C (p.Leu258=)
19g.44908992G>TCA507947628APOEc.696G>T (p.Leu232=)
c.774G>T (p.Leu258=)
gnomAD v4
19g.44908999_44909000dupCA882664505APOEc.703_704dup (p.Met236GlyfsTer16)
c.781_782dup (p.Met262GlyfsTer?)
c.781_782dup (p.Met262GlyfsTer16)
dbSNP
19g.44908999_44909000delCA2576812056APOEc.703_704del (p.Arg235AspfsTer?)
c.781_782del (p.Arg261AspfsTer?)
gnomAD v4
19g.44908997_44909000delCA2576812055APOEc.701_704del (p.Ala234GlyfsTer16)
c.779_782del (p.Ala260GlyfsTer?)
c.779_782del (p.Ala260GlyfsTer16)
19g.44908993C>ACA406304729APOEc.697C>A (p.Arg233Ser)
c.775C>A (p.Arg259Ser)
gnomAD v4
19g.44908993C=CA2338167998APOEc.697C= (p.Arg233=)
c.775C= (p.Arg259=)
19g.44908993C>GCA308885948APOEc.697C>G (p.Arg233Gly)
c.775C>G (p.Arg259Gly)
dbSNP
19g.44908993C>TCA406304732APOEc.697C>T (p.Arg233Cys)
c.775C>T (p.Arg259Cys)
dbSNP gnomAD v4
19g.44908994G>ACA406304738APOEc.698G>A (p.Arg233His)
c.776G>A (p.Arg259His)
dbSNP gnomAD v2 gnomAD v4
19g.44908994G>CCA406304742APOEc.698G>C (p.Arg233Pro)
c.776G>C (p.Arg259Pro)
gnomAD v4
19g.44908994G=CA2338167999APOEc.698G= (p.Arg233=)
c.776G= (p.Arg259=)
19g.44908994G>TCA406304736APOEc.698G>T (p.Arg233Leu)
c.776G>T (p.Arg259Leu)
gnomAD v4
19g.44908995C>ACA507947636APOEc.699C>A (p.Arg233=)
c.777C>A (p.Arg259=)
19g.44908995C=CA2338168000APOEc.699C= (p.Arg233=)
c.777C= (p.Arg259=)
19g.44908995C>GCA507947639APOEc.699C>G (p.Arg233=)
c.777C>G (p.Arg259=)
19g.44908995C>TCA507947638APOEc.699C>T (p.Arg233=)
c.777C>T (p.Arg259=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908996G>ACA406304743APOEc.700G>A (p.Ala234Thr)
c.778G>A (p.Ala260Thr)
dbSNP gnomAD v2 gnomAD v4 COSMIC
19g.44908996G>CCA406304747APOEc.700G>C (p.Ala234Pro)
c.778G>C (p.Ala260Pro)
19g.44908996G=CA2338168001APOEc.700G= (p.Ala234=)
c.778G= (p.Ala260=)
19g.44908996G>TCA406304745APOEc.700G>T (p.Ala234Ser)
c.778G>T (p.Ala260Ser)
gnomAD v4
19g.44908997C>ACA406304749APOEc.701C>A (p.Ala234Glu)
c.779C>A (p.Ala260Glu)
gnomAD v4
19g.44908997C=CA2338168002APOEc.701C= (p.Ala234=)
c.779C= (p.Ala260=)
19g.44908997C>GCA406304754APOEc.701C>G (p.Ala234Gly)
c.779C>G (p.Ala260Gly)
19g.44908997C>TCA406304752APOEc.701C>T (p.Ala234Val)
c.779C>T (p.Ala260Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908998G>ACA507947645APOEc.702G>A (p.Ala234=)
c.780G>A (p.Ala260=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.44908998G>CCA507947647APOEc.702G>C (p.Ala234=)
c.780G>C (p.Ala260=)
dbSNP gnomAD v2 gnomAD v4
19g.44908998G=CA2338168003APOEc.702G= (p.Ala234=)
c.780G= (p.Ala260=)
19g.44908998G>TCA507947648APOEc.702G>T (p.Ala234=)
c.780G>T (p.Ala260=)
gnomAD v4
19g.44908999C>ACA507947649APOEc.703C>A (p.Arg235=)
c.781C>A (p.Arg261=)
gnomAD v4
19g.44908999C=CA2338168004APOEc.703C= (p.Arg235=)
c.781C= (p.Arg261=)
19g.44908999C>GCA406304757APOEc.703C>G (p.Arg235Gly)
c.781C>G (p.Arg261Gly)
19g.44908999C>TCA9506087APOEc.703C>T (p.Arg235Trp)
c.781C>T (p.Arg261Trp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44909000G>ACA406304762APOEc.704G>A (p.Arg235Gln)
c.782G>A (p.Arg261Gln)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44909000G>CCA406304763APOEc.704G>C (p.Arg235Pro)
c.782G>C (p.Arg261Pro)
19g.44909000G=CA2338168005APOEc.704G= (p.Arg235=)
c.782G= (p.Arg261=)
19g.44909000G>TCA406304766APOEc.704G>T (p.Arg235Leu)
c.782G>T (p.Arg261Leu)
gnomAD v4
19g.44909001G>ACA507947655APOEc.705G>A (p.Arg235=)
c.783G>A (p.Arg261=)
dbSNP gnomAD v4
19g.44909001G>CCA507947656APOEc.705G>C (p.Arg235=)
c.783G>C (p.Arg261=)
19g.44909001G=CA2338168006APOEc.705G= (p.Arg235=)
c.783G= (p.Arg261=)
19g.44909001G>TCA507947657APOEc.705G>T (p.Arg235=)
c.783G>T (p.Arg261=)
gnomAD v4
19g.44909002A>CCA406304768APOEc.706A>C (p.Met236Leu)
c.784A>C (p.Met262Leu)
19g.44909002A>GCA406304770APOEc.706A>G (p.Met236Val)
c.784A>G (p.Met262Val)
19g.44909002A>TCA406304772APOEc.706A>T (p.Met236Leu)
c.784A>T (p.Met262Leu)
19g.44909003T>ACA406304773APOEc.707T>A (p.Met236Lys)
c.785T>A (p.Met262Lys)
19g.44909003T>CCA406304774APOEc.707T>C (p.Met236Thr)
c.785T>C (p.Met262Thr)
19g.44909003T>GCA406304775APOEc.707T>G (p.Met236Arg)
c.785T>G (p.Met262Arg)
19g.44909003_44909006delinsTGGACA2338168007APOEc.707_710delinsTGGA (p.Met236=)
c.785_788delinsTGGA (p.Met262=)
19g.44909004G>ACA406304788APOEc.708G>A (p.Met236Ile)
c.786G>A (p.Met262Ile)
19g.44909004G>CCA406304786APOEc.708G>C (p.Met236Ile)
c.786G>C (p.Met262Ile)
19g.44909004G=CA2338168008APOEc.708G= (p.Met236=)
c.786G= (p.Met262=)
19g.44909004G>TCA406304783APOEc.708G>T (p.Met236Ile)
c.786G>T (p.Met262Ile)
dbSNP gnomAD v4
19g.44909008_44909010delCA633478462APOEc.712_714del (p.Glu238del)
c.790_792del (p.Glu264del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched