Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908802_44908804dupCA2695228865APOEc.506_508dup (p.Asp169_Ala170insAsp)
c.584_586dup (p.Asp195_Ala196insAsp)
19g.44908804G>ACA406304149APOEc.508G>A (p.Ala170Thr)
c.586G>A (p.Ala196Thr)
gnomAD v4
19g.44908804G>CCA042396APOEc.508G>C (p.Ala170Pro)
c.586G>C (p.Ala196Pro)
dbSNP
19g.44908804G=CA2338167893APOEc.508G= (p.Ala170=)
c.586G= (p.Ala196=)
19g.44908804G>TCA406304150APOEc.508G>T (p.Ala170Ser)
c.586G>T (p.Ala196Ser)
gnomAD v4
19g.44908805C>ACA406304151APOEc.509C>A (p.Ala170Asp)
c.587C>A (p.Ala196Asp)
gnomAD v4
19g.44908805C=CA2338167894APOEc.509C= (p.Ala170=)
c.587C= (p.Ala196=)
19g.44908805C>GCA406304152APOEc.509C>G (p.Ala170Gly)
c.587C>G (p.Ala196Gly)
19g.44908805C>TCA406304153APOEc.509C>T (p.Ala170Val)
c.587C>T (p.Ala196Val)
dbSNP gnomAD v4
19g.44908806C>ACA507947830APOEc.510C>A (p.Ala170=)
c.588C>A (p.Ala196=)
gnomAD v4
19g.44908806C=CA2338167895APOEc.510C= (p.Ala170=)
c.588C= (p.Ala196=)
19g.44908806C>GCA507947831APOEc.510C>G (p.Ala170=)
c.588C>G (p.Ala196=)
gnomAD v4
19g.44908806C>TCA507947833APOEc.510C>T (p.Ala170=)
c.588C>T (p.Ala196=)
dbSNP gnomAD v2 gnomAD v4
19g.44908807G>ACA406304154APOEc.511G>A (p.Asp171Asn)
c.589G>A (p.Asp197Asn)
dbSNP gnomAD v2 gnomAD v4
19g.44908807G>CCA406304155APOEc.511G>C (p.Asp171His)
c.589G>C (p.Asp197His)
19g.44908807G=CA2338167896APOEc.511G= (p.Asp171=)
c.589G= (p.Asp197=)
19g.44908807G>TCA406304156APOEc.511G>T (p.Asp171Tyr)
c.589G>T (p.Asp197Tyr)
gnomAD v4
19g.44908808A>CCA406304159APOEc.512A>C (p.Asp171Ala)
c.590A>C (p.Asp197Ala)
19g.44908808A>GCA406304157APOEc.512A>G (p.Asp171Gly)
c.590A>G (p.Asp197Gly)
gnomAD v4
19g.44908808A>TCA406304158APOEc.512A>T (p.Asp171Val)
c.590A>T (p.Asp197Val)
19g.44908809T>ACA406304160APOEc.513T>A (p.Asp171Glu)
c.591T>A (p.Asp197Glu)
gnomAD v4
19g.44908809T>CCA507947837APOEc.513T>C (p.Asp171=)
c.591T>C (p.Asp197=)
gnomAD v4
19g.44908809T>GCA406304161APOEc.513T>G (p.Asp171Glu)
c.591T>G (p.Asp197Glu)
dbSNP
19g.44908809T=CA2338167897APOEc.513T= (p.Asp171=)
c.591T= (p.Asp197=)
19g.44908810G>ACA308885778APOEc.514G>A (p.Asp172Asn)
c.592G>A (p.Asp198Asn)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908810G>CCA406304162APOEc.514G>C (p.Asp172His)
c.592G>C (p.Asp198His)
19g.44908810G=CA2338167898APOEc.514G= (p.Asp172=)
c.592G= (p.Asp198=)
19g.44908810G>TCA406304163APOEc.514G>T (p.Asp172Tyr)
c.592G>T (p.Asp198Tyr)
gnomAD v4
19g.44908811A>CCA406304164APOEc.515A>C (p.Asp172Ala)
c.593A>C (p.Asp198Ala)
19g.44908811A>GCA406304166APOEc.515A>G (p.Asp172Gly)
c.593A>G (p.Asp198Gly)
gnomAD v4
19g.44908811A>TCA406304165APOEc.515A>T (p.Asp172Val)
c.593A>T (p.Asp198Val)
gnomAD v4
19g.44908812C>ACA9506075APOEc.516C>A (p.Asp172Glu)
c.594C>A (p.Asp198Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44908812C=CA2338167899APOEc.516C= (p.Asp172=)
c.594C= (p.Asp198=)
19g.44908812C>GCA406304167APOEc.516C>G (p.Asp172Glu)
c.594C>G (p.Asp198Glu)
19g.44908812C>TCA507947847APOEc.516C>T (p.Asp172=)
c.594C>T (p.Asp198=)
dbSNP gnomAD v4
19g.44908813C>ACA406304168APOEc.517C>A (p.Leu173Met)
c.595C>A (p.Leu199Met)
gnomAD v4
19g.44908813C=CA2338167900APOEc.517C= (p.Leu173=)
c.595C= (p.Leu199=)
19g.44908813C>GCA406304169APOEc.517C>G (p.Leu173Val)
c.595C>G (p.Leu199Val)
19g.44908813C>TCA507947852APOEc.517C>T (p.Leu173=)
c.595C>T (p.Leu199=)
dbSNP gnomAD v2 gnomAD v4
19g.44908814T>ACA406304170APOEc.518T>A (p.Leu173Gln)
c.596T>A (p.Leu199Gln)
gnomAD v4
19g.44908814T>CCA406304171APOEc.518T>C (p.Leu173Pro)
c.596T>C (p.Leu199Pro)
gnomAD v4
19g.44908814T>GCA406304172APOEc.518T>G (p.Leu173Arg)
c.596T>G (p.Leu199Arg)
19g.44908815G>ACA507947857APOEc.519G>A (p.Leu173=)
c.597G>A (p.Leu199=)
dbSNP gnomAD v2 gnomAD v4
19g.44908815G>CCA507947858APOEc.519G>C (p.Leu173=)
c.597G>C (p.Leu199=)
gnomAD v4
19g.44908815G=CA2338167901APOEc.519G= (p.Leu173=)
c.597G= (p.Leu199=)
19g.44908815G>TCA507947861APOEc.519G>T (p.Leu173=)
c.597G>T (p.Leu199=)
gnomAD v4
19g.44908816C>ACA406304173APOEc.520C>A (p.Gln174Lys)
c.598C>A (p.Gln200Lys)
dbSNP gnomAD v2 gnomAD v4
19g.44908816C=CA2338167902APOEc.520C= (p.Gln174=)
c.598C= (p.Gln200=)
19g.44908816C>GCA406304174APOEc.520C>G (p.Gln174Glu)
c.598C>G (p.Gln200Glu)
19g.44908816C>TCA406304175APOEc.520C>T (p.Gln174Ter)
c.598C>T (p.Gln200Ter)
gnomAD v4
19g.44908817_44908870delCA2695228866APOEc.521_574del (p.Gln174_Gly191del)
c.599_652del (p.Gln200_Gly217del)
19g.44908817A>CCA406304176APOEc.521A>C (p.Gln174Pro)
c.599A>C (p.Gln200Pro)
19g.44908817A>GCA406304178APOEc.521A>G (p.Gln174Arg)
c.599A>G (p.Gln200Arg)
gnomAD v4
19g.44908817A>TCA406304177APOEc.521A>T (p.Gln174Leu)
c.599A>T (p.Gln200Leu)
19g.44908818_44908819delCA2814526233APOEc.522_523del (p.Lys175AlafsTer?)
c.600_601del (p.Lys201AlafsTer?)
19g.44908818G>ACA507947868APOEc.522G>A (p.Gln174=)
c.600G>A (p.Gln200=)
dbSNP gnomAD v2 gnomAD v4
19g.44908818G>CCA406304179APOEc.522G>C (p.Gln174His)
c.600G>C (p.Gln200His)
gnomAD v4
19g.44908818G=CA2338167903APOEc.522G= (p.Gln174=)
c.600G= (p.Gln200=)
19g.44908818G>TCA406304180APOEc.522G>T (p.Gln174His)
c.600G>T (p.Gln200His)
19g.44908819A>CCA406304181APOEc.523A>C (p.Lys175Gln)
c.601A>C (p.Lys201Gln)
19g.44908819A>GCA406304182APOEc.523A>G (p.Lys175Glu)
c.601A>G (p.Lys201Glu)
19g.44908819A>TCA406304183APOEc.523A>T (p.Lys175Ter)
c.601A>T (p.Lys201Ter)
19g.44908820A>CCA406304184APOEc.524A>C (p.Lys175Thr)
c.602A>C (p.Lys201Thr)
19g.44908820A>GCA406304185APOEc.524A>G (p.Lys175Arg)
c.602A>G (p.Lys201Arg)
19g.44908820A>TCA406304186APOEc.524A>T (p.Lys175Met)
c.602A>T (p.Lys201Met)
gnomAD v4
19g.44908821G>ACA507947877APOEc.525G>A (p.Lys175=)
c.603G>A (p.Lys201=)
gnomAD v4
19g.44908821G>CCA406304187APOEc.525G>C (p.Lys175Asn)
c.603G>C (p.Lys201Asn)
19g.44908821G>TCA406304188APOEc.525G>T (p.Lys175Asn)
c.603G>T (p.Lys201Asn)
gnomAD v4
19g.44908822C>ACA406304189APOEc.526C>A (p.Arg176Ser)
c.604C>A (p.Arg202Ser)
gnomAD v4
19g.44908822C=CA2338167904APOEc.526C= (p.Arg176=)
c.604C= (p.Arg202=)
19g.44908822C>GCA406304190APOEc.526C>G (p.Arg176Gly)
c.604C>G (p.Arg202Gly)
19g.44908822C>TCA127498APOEc.526C>T (p.Arg176Cys)
c.604C>T (p.Arg202Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.[44908822C>T;44909021G>A]CA041377APOEc.[526C>T;725G>A] (p.[Arg176Cys;Arg242Gln])
c.[604C>T;803G>A] (p.[Arg202Cys;Arg268Gln])
ClinVar
19g.[44908822C>T;44909057T>A]CA041493APOEc.[526C>T;761T>A] (p.[Arg176Cys;Val254Glu])
c.[604C>T;839T>A] (p.[Arg202Cys;Val280Glu])
ClinVar
19g.44908823G>ACA406304193APOEc.527G>A (p.Arg176His)
c.605G>A (p.Arg202His)
COSMIC
19g.44908823G>CCA406304192APOEc.527G>C (p.Arg176Pro)
c.605G>C (p.Arg202Pro)
19g.44908823G>TCA406304191APOEc.527G>T (p.Arg176Leu)
c.605G>T (p.Arg202Leu)
gnomAD v4
19g.44908824C>ACA507947882APOEc.528C>A (p.Arg176=)
c.606C>A (p.Arg202=)
gnomAD v4
19g.44908824C=CA2338167905APOEc.528C= (p.Arg176=)
c.606C= (p.Arg202=)
19g.44908824C>GCA507947883APOEc.528C>G (p.Arg176=)
c.606C>G (p.Arg202=)
19g.44908824C>TCA507947884APOEc.528C>T (p.Arg176=)
c.606C>T (p.Arg202=)
dbSNP gnomAD v4
19g.44908825C>ACA406304194APOEc.529C>A (p.Leu177Met)
c.607C>A (p.Leu203Met)
gnomAD v4
19g.44908825C=CA2338167906APOEc.529C= (p.Leu177=)
c.607C= (p.Leu203=)
19g.44908825C>GCA406304195APOEc.529C>G (p.Leu177Val)
c.607C>G (p.Leu203Val)
19g.44908825C>TCA507947885APOEc.529C>T (p.Leu177=)
c.607C>T (p.Leu203=)
dbSNP gnomAD v2 gnomAD v4
19g.44908826_44908827insTCTACGTGATATGCTTTTTCACCAGAACCACCATTTAGAATTTCTTCTAATTTATTATATTGATCTAACATCCATTCGATGTAAGTTTTTCCGTCTCA2510558622APOEc.530_531insTCTACGTGATATGCTTTTTCACCAGAACCACCATTTAGAATTTCTTCTAATTTATTATATTGATCTAACATCCATTCGATGTAAGTTTTTCCGTCT (p.Leu177_Ala178insLeuArgAspMetLeuPheHisGlnAsnHisHisLeuGluPheLeuLeuIleTyrTyrIleAspLeuThrSerIleArgCysLysPhePheArgLeu)
c.608_609insTCTACGTGATATGCTTTTTCACCAGAACCACCATTTAGAATTTCTTCTAATTTATTATATTGATCTAACATCCATTCGATGTAAGTTTTTCCGTCT (p.Leu203_Ala204insLeuArgAspMetLeuPheHisGlnAsnHisHisLeuGluPheLeuLeuIleTyrTyrIleAspLeuThrSerIleArgCysLysPhePheArgLeu)
19g.44908826T>ACA406304196APOEc.530T>A (p.Leu177Gln)
c.608T>A (p.Leu203Gln)
19g.44908826T>CCA406304197APOEc.530T>C (p.Leu177Pro)
c.608T>C (p.Leu203Pro)
gnomAD v4
19g.44908826T>GCA406304198APOEc.530T>G (p.Leu177Arg)
c.608T>G (p.Leu203Arg)
19g.44908827G>ACA507947887APOEc.531G>A (p.Leu177=)
c.609G>A (p.Leu203=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908827G>CCA507947889APOEc.531G>C (p.Leu177=)
c.609G>C (p.Leu203=)
19g.44908827G=CA2338167907APOEc.531G= (p.Leu177=)
c.609G= (p.Leu203=)
19g.44908827G>TCA507947890APOEc.531G>T (p.Leu177=)
c.609G>T (p.Leu203=)
gnomAD v4
19g.44908828G>ACA406304199APOEc.532G>A (p.Ala178Thr)
c.610G>A (p.Ala204Thr)
gnomAD v4
19g.44908828G>CCA406304200APOEc.532G>C (p.Ala178Pro)
c.610G>C (p.Ala204Pro)
19g.44908828G>TCA406304201APOEc.532G>T (p.Ala178Ser)
c.610G>T (p.Ala204Ser)
gnomAD v4
19g.44908829C>ACA406304202APOEc.533C>A (p.Ala178Glu)
c.611C>A (p.Ala204Glu)
gnomAD v4
19g.44908829C>GCA406304203APOEc.533C>G (p.Ala178Gly)
c.611C>G (p.Ala204Gly)
19g.44908829C>TCA406304204APOEc.533C>T (p.Ala178Val)
c.611C>T (p.Ala204Val)
gnomAD v4
19g.44908830A=CA2338167908APOEc.534A= (p.Ala178=)
c.612A= (p.Ala204=)
19g.44908830A>CCA507947892APOEc.534A>C (p.Ala178=)
c.612A>C (p.Ala204=)
19g.44908830A>GCA507947893APOEc.534A>G (p.Ala178=)
c.612A>G (p.Ala204=)
gnomAD v4
19g.44908830A>TCA507947894APOEc.534A>T (p.Ala178=)
c.612A>T (p.Ala204=)
dbSNP gnomAD v4
19g.44908831G>ACA406304205APOEc.535G>A (p.Val179Met)
c.613G>A (p.Val205Met)
19g.44908831G>CCA406304206APOEc.535G>C (p.Val179Leu)
c.613G>C (p.Val205Leu)
19g.44908831G>TCA406304207APOEc.535G>T (p.Val179Leu)
c.613G>T (p.Val205Leu)
19g.44908832T>ACA406304210APOEc.536T>A (p.Val179Glu)
c.614T>A (p.Val205Glu)
gnomAD v4
19g.44908832T>CCA406304209APOEc.536T>C (p.Val179Ala)
c.614T>C (p.Val205Ala)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908832T>GCA406304208APOEc.536T>G (p.Val179Gly)
c.614T>G (p.Val205Gly)
19g.44908832T=CA2338167909APOEc.536T= (p.Val179=)
c.614T= (p.Val205=)
19g.44908833G>ACA507947895APOEc.537G>A (p.Val179=)
c.615G>A (p.Val205=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.44908833G>CCA507947896APOEc.537G>C (p.Val179=)
c.615G>C (p.Val205=)
19g.44908833G=CA2338167910APOEc.537G= (p.Val179=)
c.615G= (p.Val205=)
19g.44908833G>TCA507947897APOEc.537G>T (p.Val179=)
c.615G>T (p.Val205=)
19g.44908834T>ACA406304211APOEc.538T>A (p.Tyr180Asn)
c.616T>A (p.Tyr206Asn)
gnomAD v4
19g.44908834T>CCA9506076APOEc.538T>C (p.Tyr180His)
c.616T>C (p.Tyr206His)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44908834T>GCA406304212APOEc.538T>G (p.Tyr180Asp)
c.616T>G (p.Tyr206Asp)
dbSNP
19g.44908834T=CA2338167911APOEc.538T= (p.Tyr180=)
c.616T= (p.Tyr206=)
19g.44908835A>CCA406304213APOEc.539A>C (p.Tyr180Ser)
c.617A>C (p.Tyr206Ser)
19g.44908835A>GCA406304214APOEc.539A>G (p.Tyr180Cys)
c.617A>G (p.Tyr206Cys)
19g.44908835A>TCA406304215APOEc.539A>T (p.Tyr180Phe)
c.617A>T (p.Tyr206Phe)
19g.44908836C>ACA406304216APOEc.540C>A (p.Tyr180Ter)
c.618C>A (p.Tyr206Ter)
dbSNP gnomAD v2 gnomAD v4
19g.44908836C=CA2338167912APOEc.540C= (p.Tyr180=)
c.618C= (p.Tyr206=)
19g.44908836C>GCA406304217APOEc.540C>G (p.Tyr180Ter)
c.618C>G (p.Tyr206Ter)
19g.44908836C>TCA507947901APOEc.540C>T (p.Tyr180=)
c.618C>T (p.Tyr206=)
gnomAD v4
19g.44908837delCA2585715443APOEc.541del (p.Gln181ArgfsTer?)
c.619del (p.Gln207ArgfsTer?)
gnomAD v4
19g.44908837C>ACA406304218APOEc.541C>A (p.Gln181Lys)
c.619C>A (p.Gln207Lys)
dbSNP gnomAD v4
19g.44908837C=CA2338167913APOEc.541C= (p.Gln181=)
c.619C= (p.Gln207=)
19g.44908837C>GCA406304219APOEc.541C>G (p.Gln181Glu)
c.619C>G (p.Gln207Glu)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908837C>TCA406304220APOEc.541C>T (p.Gln181Ter)
c.619C>T (p.Gln207Ter)
gnomAD v4
19g.44908838A=CA2740130015APOEc.542A= (p.Gln181=)
c.620A= (p.Gln207=)
19g.44908838A>CCA406304221APOEc.542A>C (p.Gln181Pro)
c.620A>C (p.Gln207Pro)
19g.44908838A>GCA406304222APOEc.542A>G (p.Gln181Arg)
c.620A>G (p.Gln207Arg)
gnomAD v4
19g.44908838A>TCA406304223APOEc.542A>T (p.Gln181Leu)
c.620A>T (p.Gln207Leu)
ClinVar
19g.44908839G>ACA507947906APOEc.543G>A (p.Gln181=)
c.621G>A (p.Gln207=)
dbSNP gnomAD v2 gnomAD v4
19g.44908839G>CCA406304224APOEc.543G>C (p.Gln181His)
c.621G>C (p.Gln207His)
dbSNP gnomAD v2 gnomAD v4
19g.44908839G=CA2338167914APOEc.543G= (p.Gln181=)
c.621G= (p.Gln207=)
19g.44908839G>TCA9506077APOEc.543G>T (p.Gln181His)
c.621G>T (p.Gln207His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908840G>ACA406304225APOEc.544G>A (p.Ala182Thr)
c.622G>A (p.Ala208Thr)
gnomAD v4
19g.44908840G>CCA308885811APOEc.544G>C (p.Ala182Pro)
c.622G>C (p.Ala208Pro)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.44908840G=CA2338167915APOEc.544G= (p.Ala182=)
c.622G= (p.Ala208=)
19g.44908840G>TCA308885815APOEc.544G>T (p.Ala182Ser)
c.622G>T (p.Ala208Ser)
dbSNP gnomAD v4 COSMIC
19g.44908840_44908841delinsGCCA2338167916APOEc.544_545delinsGC (p.Ala182=)
c.622_623delinsGC (p.Ala208=)
19g.44908841C>ACA406304226APOEc.545C>A (p.Ala182Asp)
c.623C>A (p.Ala208Asp)
gnomAD v4
19g.44908841C>GCA406304227APOEc.545C>G (p.Ala182Gly)
c.623C>G (p.Ala208Gly)
19g.44908841C>TCA406304228APOEc.545C>T (p.Ala182Val)
c.623C>T (p.Ala208Val)
dbSNP gnomAD v4
19g.44908842delCA882664255APOEc.546del (p.Ala184ProfsTer?)
c.624del (p.Ala210ProfsTer?)
dbSNP gnomAD v3 gnomAD v4
19g.44908842C>ACA507947912APOEc.546C>A (p.Ala182=)
c.624C>A (p.Ala208=)
dbSNP gnomAD v4
19g.44908842C=CA2338167917APOEc.546C= (p.Ala182=)
c.624C= (p.Ala208=)
19g.44908842C>GCA507947913APOEc.546C>G (p.Ala182=)
c.624C>G (p.Ala208=)
19g.44908842C>TCA507947914APOEc.546C>T (p.Ala182=)
c.624C>T (p.Ala208=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908842_44908843insAGTCA2585715444APOEc.546_547insAGT (p.Ala182_Gly183insSer)
c.624_625insAGT (p.Ala208_Gly209insSer)
gnomAD v4
19g.44908843G>ACA406304229APOEc.547G>A (p.Gly183Arg)
c.625G>A (p.Gly209Arg)
dbSNP gnomAD v3 gnomAD v4 COSMIC
19g.44908843G>CCA406304230APOEc.547G>C (p.Gly183Arg)
c.625G>C (p.Gly209Arg)
dbSNP gnomAD v2 gnomAD v4
19g.44908843G=CA2338167918APOEc.547G= (p.Gly183=)
c.625G= (p.Gly209=)
19g.44908843G>TCA406304231APOEc.547G>T (p.Gly183Trp)
c.625G>T (p.Gly209Trp)
dbSNP gnomAD v4
19g.44908846delCA2585715445APOEc.550del (p.Ala184ProfsTer?)
c.628del (p.Ala210ProfsTer?)
gnomAD v4
19g.44908844G>ACA406304232APOEc.548G>A (p.Gly183Glu)
c.626G>A (p.Gly209Glu)
gnomAD v4
19g.44908844G>CCA406304233APOEc.548G>C (p.Gly183Ala)
c.626G>C (p.Gly209Ala)
ClinVar dbSNP
19g.44908844G=CA2740130016APOEc.548G= (p.Gly183=)
c.626G= (p.Gly209=)
19g.44908844G>TCA406304234APOEc.548G>T (p.Gly183Val)
c.626G>T (p.Gly209Val)
19g.44908845G>ACA507947916APOEc.549G>A (p.Gly183=)
c.627G>A (p.Gly209=)
gnomAD v4
19g.44908845G>CCA507947918APOEc.549G>C (p.Gly183=)
c.627G>C (p.Gly209=)
19g.44908845G>TCA507947919APOEc.549G>T (p.Gly183=)
c.627G>T (p.Gly209=)
19g.44908846G>ACA406304235APOEc.550G>A (p.Ala184Thr)
c.628G>A (p.Ala210Thr)
dbSNP gnomAD v2 gnomAD v4 COSMIC
19g.44908846G>CCA406304237APOEc.550G>C (p.Ala184Pro)
c.628G>C (p.Ala210Pro)
19g.44908846G=CA2338167919APOEc.550G= (p.Ala184=)
c.628G= (p.Ala210=)
19g.44908846G>TCA406304236APOEc.550G>T (p.Ala184Ser)
c.628G>T (p.Ala210Ser)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908847C>ACA308885824APOEc.551C>A (p.Ala184Asp)
c.629C>A (p.Ala210Asp)
dbSNP gnomAD v4
19g.44908847C=CA2338167920APOEc.551C= (p.Ala184=)
c.629C= (p.Ala210=)
19g.44908847C>GCA406304239APOEc.551C>G (p.Ala184Gly)
c.629C>G (p.Ala210Gly)
19g.44908847C>TCA406304238APOEc.551C>T (p.Ala184Val)
c.629C>T (p.Ala210Val)
dbSNP gnomAD v4
19g.44908847_44908848insTCA2509051181APOEc.551_552insT (p.Arg185ProfsTer?)
c.629_630insT (p.Arg211ProfsTer?)
19g.44908848C>ACA507947920APOEc.552C>A (p.Ala184=)
c.630C>A (p.Ala210=)
dbSNP gnomAD v4
19g.44908848C=CA2338167921APOEc.552C= (p.Ala184=)
c.630C= (p.Ala210=)
19g.44908848C>GCA507947921APOEc.552C>G (p.Ala184=)
c.630C>G (p.Ala210=)
19g.44908848C>TCA507947922APOEc.552C>T (p.Ala184=)
c.630C>T (p.Ala210=)
ClinVar
19g.44908848_44908852delCA2585715446APOEc.552_556del (p.Arg185GlyfsTer?)
c.630_634del (p.Arg211GlyfsTer?)
gnomAD v4
19g.44908849C>ACA406304240APOEc.553C>A (p.Arg185Ser)
c.631C>A (p.Arg211Ser)
gnomAD v4
19g.44908849C>GCA406304241APOEc.553C>G (p.Arg185Gly)
c.631C>G (p.Arg211Gly)
19g.44908849C>TCA406304242APOEc.553C>T (p.Arg185Cys)
c.631C>T (p.Arg211Cys)
gnomAD v4
19g.44908851_44908852delCA2585715447APOEc.555_556del (p.Glu186GlyfsTer?)
c.633_634del (p.Glu212GlyfsTer?)
gnomAD v4
19g.44908850G>ACA406304243APOEc.554G>A (p.Arg185His)
c.632G>A (p.Arg211His)
dbSNP gnomAD v2 gnomAD v4
19g.44908850G>CCA406304244APOEc.554G>C (p.Arg185Pro)
c.632G>C (p.Arg211Pro)
dbSNP gnomAD v2 gnomAD v4
19g.44908850G=CA2338167922APOEc.554G= (p.Arg185=)
c.632G= (p.Arg211=)
19g.44908850G>TCA406304245APOEc.554G>T (p.Arg185Leu)
c.632G>T (p.Arg211Leu)
dbSNP gnomAD v4
19g.44908851C>ACA507947364APOEc.555C>A (p.Arg185=)
c.633C>A (p.Arg211=)
gnomAD v4
19g.44908851C=CA2338167923APOEc.555C= (p.Arg185=)
c.633C= (p.Arg211=)
19g.44908851C>GCA507947363APOEc.555C>G (p.Arg185=)
c.633C>G (p.Arg211=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908851C>TCA9506078APOEc.555C>T (p.Arg185=)
c.633C>T (p.Arg211=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908852G>ACA406304246APOEc.556G>A (p.Glu186Lys)
c.634G>A (p.Glu212Lys)
dbSNP gnomAD v4
19g.44908852G>CCA406304247APOEc.556G>C (p.Glu186Gln)
c.634G>C (p.Glu212Gln)
gnomAD v4
19g.44908852G=CA2338167924APOEc.556G= (p.Glu186=)
c.634G= (p.Glu212=)
19g.44908852G>TCA406304248APOEc.556G>T (p.Glu186Ter)
c.634G>T (p.Glu212Ter)
gnomAD v4
19g.44908853A>CCA406304251APOEc.557A>C (p.Glu186Ala)
c.635A>C (p.Glu212Ala)
19g.44908853A>GCA406304250APOEc.557A>G (p.Glu186Gly)
c.635A>G (p.Glu212Gly)
gnomAD v4
19g.44908853A>TCA406304249APOEc.557A>T (p.Glu186Val)
c.635A>T (p.Glu212Val)
19g.44908854G>ACA507947365APOEc.558G>A (p.Glu186=)
c.636G>A (p.Glu212=)
dbSNP gnomAD v2 gnomAD v4
19g.44908854G>CCA406304252APOEc.558G>C (p.Glu186Asp)
c.636G>C (p.Glu212Asp)
gnomAD v4
19g.44908854G=CA2338167925APOEc.558G= (p.Glu186=)
c.636G= (p.Glu212=)
19g.44908854G>TCA406304253APOEc.558G>T (p.Glu186Asp)
c.636G>T (p.Glu212Asp)
19g.44908855G>ACA406304254APOEc.559G>A (p.Gly187Ser)
c.637G>A (p.Gly213Ser)
19g.44908855G>CCA406304255APOEc.559G>C (p.Gly187Arg)
c.637G>C (p.Gly213Arg)
dbSNP
19g.44908855G=CA2338167926APOEc.559G= (p.Gly187=)
c.637G= (p.Gly213=)
19g.44908855G>TCA406304256APOEc.559G>T (p.Gly187Cys)
c.637G>T (p.Gly213Cys)
19g.44908855_44908859delCA2585715448APOEc.559_563del (p.Gly187ArgfsTer?)
c.637_641del (p.Gly213ArgfsTer?)
gnomAD v4
19g.44908856G>ACA406304257APOEc.560G>A (p.Gly187Asp)
c.638G>A (p.Gly213Asp)
gnomAD v4
19g.44908856G>CCA406304258APOEc.560G>C (p.Gly187Ala)
c.638G>C (p.Gly213Ala)
dbSNP gnomAD v2 gnomAD v4
19g.44908856G=CA2338167927APOEc.560G= (p.Gly187=)
c.638G= (p.Gly213=)
19g.44908856G>TCA406304259APOEc.560G>T (p.Gly187Val)
c.638G>T (p.Gly213Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908857C>ACA507947366APOEc.561C>A (p.Gly187=)
c.639C>A (p.Gly213=)
gnomAD v4
19g.44908857C>GCA507947367APOEc.561C>G (p.Gly187=)
c.639C>G (p.Gly213=)
19g.44908857C>TCA507947368APOEc.561C>T (p.Gly187=)
c.639C>T (p.Gly213=)
gnomAD v3 gnomAD v4
19g.44908858G>ACA406304260APOEc.562G>A (p.Ala188Thr)
c.640G>A (p.Ala214Thr)
gnomAD v4
19g.44908858G>CCA406304261APOEc.562G>C (p.Ala188Pro)
c.640G>C (p.Ala214Pro)
dbSNP
19g.44908858G>TCA406304262APOEc.562G>T (p.Ala188Ser)
c.640G>T (p.Ala214Ser)
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)
19g.44908872C>ACA507947383APOEc.576C>A (p.Leu192=)
c.654C>A (p.Leu218=)
gnomAD v4
19g.44908872C=CA2338167936APOEc.576C= (p.Leu192=)
c.654C= (p.Leu218=)
19g.44908872C>GCA507947382APOEc.576C>G (p.Leu192=)
c.654C>G (p.Leu218=)
dbSNP
19g.44908872C>TCA507947380APOEc.576C>T (p.Leu192=)
c.654C>T (p.Leu218=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908873A>CCA406304290APOEc.577A>C (p.Ser193Arg)
c.655A>C (p.Ser219Arg)
19g.44908873A>GCA406304291APOEc.577A>G (p.Ser193Gly)
c.655A>G (p.Ser219Gly)
gnomAD v4
19g.44908873A>TCA406304292APOEc.577A>T (p.Ser193Cys)
c.655A>T (p.Ser219Cys)
19g.44908874G>ACA406304294APOEc.578G>A (p.Ser193Asn)
c.656G>A (p.Ser219Asn)
19g.44908874G>CCA406304295APOEc.578G>C (p.Ser193Thr)
c.656G>C (p.Ser219Thr)
19g.44908874G>TCA406304293APOEc.578G>T (p.Ser193Ile)
c.656G>T (p.Ser219Ile)
19g.44908875C>ACA406304296APOEc.579C>A (p.Ser193Arg)
c.657C>A (p.Ser219Arg)
dbSNP
19g.44908875C=CA2338167937APOEc.579C= (p.Ser193=)
c.657C= (p.Ser219=)
19g.44908875C>GCA9506079APOEc.579C>G (p.Ser193Arg)
c.657C>G (p.Ser219Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44908875C>TCA507947386APOEc.579C>T (p.Ser193=)
c.657C>T (p.Ser219=)
dbSNP gnomAD v4
19g.44908876G>ACA406304298APOEc.580G>A (p.Ala194Thr)
c.658G>A (p.Ala220Thr)
dbSNP gnomAD v4 COSMIC
19g.44908876G>CCA406304297APOEc.580G>C (p.Ala194Pro)
c.658G>C (p.Ala220Pro)
19g.44908876G=CA2338167938APOEc.580G= (p.Ala194=)
c.658G= (p.Ala220=)
19g.44908876G>TCA406304299APOEc.580G>T (p.Ala194Ser)
c.658G>T (p.Ala220Ser)
19g.44908877C>ACA406304300APOEc.581C>A (p.Ala194Asp)
c.659C>A (p.Ala220Asp)
19g.44908877C>GCA406304301APOEc.581C>G (p.Ala194Gly)
c.659C>G (p.Ala220Gly)
19g.44908877C>TCA406304302APOEc.581C>T (p.Ala194Val)
c.659C>T (p.Ala220Val)
19g.44908878delCA2695228867APOEc.582del (p.Ile195SerfsTer?)
c.660del (p.Ile221SerfsTer?)
19g.44908878C>ACA507947390APOEc.582C>A (p.Ala194=)
c.660C>A (p.Ala220=)
19g.44908878C>GCA507947392APOEc.582C>G (p.Ala194=)
c.660C>G (p.Ala220=)
19g.44908878C>TCA507947391APOEc.582C>T (p.Ala194=)
c.660C>T (p.Ala220=)
gnomAD v4
19g.44908879A=CA2338167939APOEc.583A= (p.Ile195=)
c.661A= (p.Ile221=)
19g.44908879A>CCA406304304APOEc.583A>C (p.Ile195Leu)
c.661A>C (p.Ile221Leu)
19g.44908879A>GCA406304306APOEc.583A>G (p.Ile195Val)
c.661A>G (p.Ile221Val)
19g.44908879A>TCA406304307APOEc.583A>T (p.Ile195Phe)
c.661A>T (p.Ile221Phe)
ClinVar dbSNP gnomAD v4
19g.44908880T>ACA406304308APOEc.584T>A (p.Ile195Asn)
c.662T>A (p.Ile221Asn)
19g.44908880T>CCA406304309APOEc.584T>C (p.Ile195Thr)
c.662T>C (p.Ile221Thr)
19g.44908880T>GCA406304311APOEc.584T>G (p.Ile195Ser)
c.662T>G (p.Ile221Ser)
19g.44908881C>ACA507947394APOEc.585C>A (p.Ile195=)
c.663C>A (p.Ile221=)
19g.44908881C=CA2338167940APOEc.585C= (p.Ile195=)
c.663C= (p.Ile221=)
19g.44908881C>GCA406304312APOEc.585C>G (p.Ile195Met)
c.663C>G (p.Ile221Met)
dbSNP gnomAD v2 gnomAD v4
19g.44908881C>TCA507947396APOEc.585C>T (p.Ile195=)
c.663C>T (p.Ile221=)
dbSNP gnomAD v4
19g.44908882C>ACA406304315APOEc.586C>A (p.Arg196Ser)
c.664C>A (p.Arg222Ser)
gnomAD v4
19g.44908882C=CA2338167941APOEc.586C= (p.Arg196=)
c.664C= (p.Arg222=)
19g.44908882C>GCA406304314APOEc.586C>G (p.Arg196Gly)
c.664C>G (p.Arg222Gly)
19g.44908882C>TCA9506080APOEc.586C>T (p.Arg196Cys)
c.664C>T (p.Arg222Cys)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.44908883G>ACA9506081APOEc.587G>A (p.Arg196His)
c.665G>A (p.Arg222His)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44908883G>CCA406304316APOEc.587G>C (p.Arg196Pro)
c.665G>C (p.Arg222Pro)
gnomAD v4
19g.44908883G=CA2338167942APOEc.587G= (p.Arg196=)
c.665G= (p.Arg222=)
19g.44908883G>TCA406304317APOEc.587G>T (p.Arg196Leu)
c.665G>T (p.Arg222Leu)
gnomAD v4
19g.44908884C>ACA308885886APOEc.588C>A (p.Arg196=)
c.666C>A (p.Arg222=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908884C=CA2338167943APOEc.588C= (p.Arg196=)
c.666C= (p.Arg222=)
19g.44908884C>GCA507947400APOEc.588C>G (p.Arg196=)
c.666C>G (p.Arg222=)
19g.44908884C>TCA507947401APOEc.588C>T (p.Arg196=)
c.666C>T (p.Arg222=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.44908885G>ACA406304319APOEc.589G>A (p.Glu197Lys)
c.667G>A (p.Glu223Lys)
gnomAD v4
19g.44908885G>CCA406304320APOEc.589G>C (p.Glu197Gln)
c.667G>C (p.Glu223Gln)
19g.44908885G>TCA406304322APOEc.589G>T (p.Glu197Ter)
c.667G>T (p.Glu223Ter)
dbSNP gnomAD v4
19g.44908886A=CA2338167944APOEc.590A= (p.Glu197=)
c.668A= (p.Glu223=)
19g.44908886A>CCA406304323APOEc.590A>C (p.Glu197Ala)
c.668A>C (p.Glu223Ala)
19g.44908886A>GCA406304324APOEc.590A>G (p.Glu197Gly)
c.668A>G (p.Glu223Gly)
dbSNP
19g.44908886A>TCA406304325APOEc.590A>T (p.Glu197Val)
c.668A>T (p.Glu223Val)
19g.44908887G>ACA308885887APOEc.591G>A (p.Glu197=)
c.669G>A (p.Glu223=)
ClinVar dbSNP gnomAD v4
19g.44908887G>CCA406304327APOEc.591G>C (p.Glu197Asp)
c.669G>C (p.Glu223Asp)
19g.44908887G=CA2338167945APOEc.591G= (p.Glu197=)
c.669G= (p.Glu223=)
19g.44908887G>TCA406304329APOEc.591G>T (p.Glu197Asp)
c.669G>T (p.Glu223Asp)
19g.44908888C>ACA406304332APOEc.592C>A (p.Arg198Ser)
c.670C>A (p.Arg224Ser)
gnomAD v4
19g.44908888C=CA2338167946APOEc.592C= (p.Arg198=)
c.670C= (p.Arg224=)
19g.44908888C>GCA406304333APOEc.592C>G (p.Arg198Gly)
c.670C>G (p.Arg224Gly)
19g.44908888C>TCA406304331APOEc.592C>T (p.Arg198Cys)
c.670C>T (p.Arg224Cys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908889G>ACA406304335APOEc.593G>A (p.Arg198His)
c.671G>A (p.Arg224His)
gnomAD v4
19g.44908889G>CCA406304336APOEc.593G>C (p.Arg198Pro)
c.671G>C (p.Arg224Pro)
19g.44908889G=CA2338167947APOEc.593G= (p.Arg198=)
c.671G= (p.Arg224=)
19g.44908889G>TCA308885889APOEc.593G>T (p.Arg198Leu)
c.671G>T (p.Arg224Leu)
dbSNP gnomAD v4
19g.44908890C>ACA507947405APOEc.594C>A (p.Arg198=)
c.672C>A (p.Arg224=)
19g.44908890C=CA2338167948APOEc.594C= (p.Arg198=)
c.672C= (p.Arg224=)
19g.44908890C>GCA507947406APOEc.594C>G (p.Arg198=)
c.672C>G (p.Arg224=)
19g.44908890C>TCA507947407APOEc.594C>T (p.Arg198=)
c.672C>T (p.Arg224=)
dbSNP
19g.44908891C>ACA406304337APOEc.595C>A (p.Leu199Met)
c.673C>A (p.Leu225Met)
19g.44908891C>GCA406304338APOEc.595C>G (p.Leu199Val)
c.673C>G (p.Leu225Val)
19g.44908891C>TCA507947408APOEc.595C>T (p.Leu199=)
c.673C>T (p.Leu225=)
19g.44908891_44908892delCA2695228868APOEc.595_596del (p.Leu199GlyfsTer?)
c.673_674del (p.Leu225GlyfsTer?)
19g.44908892T>ACA406304339APOEc.596T>A (p.Leu199Gln)
c.674T>A (p.Leu225Gln)
19g.44908892T>CCA406304340APOEc.596T>C (p.Leu199Pro)
c.674T>C (p.Leu225Pro)
gnomAD v4
19g.44908892T>GCA308885893APOEc.596T>G (p.Leu199Arg)
c.674T>G (p.Leu225Arg)
dbSNP
19g.44908892T=CA2338167949APOEc.596T= (p.Leu199=)
c.674T= (p.Leu225=)
19g.44908893G>ACA507947410APOEc.597G>A (p.Leu199=)
c.675G>A (p.Leu225=)
COSMIC
19g.44908893G>CCA507947411APOEc.597G>C (p.Leu199=)
c.675G>C (p.Leu225=)
19g.44908893G=CA2338167950APOEc.597G= (p.Leu199=)
c.675G= (p.Leu225=)
19g.44908893G>TCA507947409APOEc.597G>T (p.Leu199=)
c.675G>T (p.Leu225=)
dbSNP gnomAD v2 gnomAD v4
19g.44908896delCA2585715449APOEc.600del (p.Leu202TrpfsTer?)
c.678del (p.Leu228TrpfsTer?)
gnomAD v4
19g.44908894G>ACA406304341APOEc.598G>A (p.Gly200Arg)
c.676G>A (p.Gly226Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908894G>CCA406304342APOEc.598G>C (p.Gly200Arg)
c.676G>C (p.Gly226Arg)
ClinVar
19g.44908894G=CA2338167951APOEc.598G= (p.Gly200=)
c.676G= (p.Gly226=)
19g.44908894G>TCA406304343APOEc.598G>T (p.Gly200Trp)
c.676G>T (p.Gly226Trp)
19g.44908895G>ACA406304347APOEc.599G>A (p.Gly200Glu)
c.677G>A (p.Gly226Glu)
gnomAD v4
19g.44908895G>CCA406304349APOEc.599G>C (p.Gly200Ala)
c.677G>C (p.Gly226Ala)
19g.44908895G>TCA406304345APOEc.599G>T (p.Gly200Val)
c.677G>T (p.Gly226Val)
19g.44908896G>ACA507947414APOEc.600G>A (p.Gly200=)
c.678G>A (p.Gly226=)
gnomAD v4 COSMIC
19g.44908896G>CCA507947416APOEc.600G>C (p.Gly200=)
c.678G>C (p.Gly226=)
dbSNP
19g.44908896G=CA2338167952APOEc.600G= (p.Gly200=)
c.678G= (p.Gly226=)
19g.44908896G>TCA507947417APOEc.600G>T (p.Gly200=)
c.678G>T (p.Gly226=)
19g.44908897C>ACA406304350APOEc.601C>A (p.Pro201Thr)
c.679C>A (p.Pro227Thr)
19g.44908897C>GCA406304351APOEc.601C>G (p.Pro201Ala)
c.679C>G (p.Pro227Ala)
gnomAD v4
19g.44908897C>TCA406304353APOEc.601C>T (p.Pro201Ser)
c.679C>T (p.Pro227Ser)
gnomAD v4
19g.44908900dupCA2585715450APOEc.604dup (p.Leu202ProfsTer?)
c.682dup (p.Leu228ProfsTer?)
gnomAD v4
19g.44908900delCA2585715451APOEc.604del (p.Leu202TrpfsTer?)
c.682del (p.Leu228TrpfsTer?)
gnomAD v4
19g.44908898C>ACA406304355APOEc.602C>A (p.Pro201His)
c.680C>A (p.Pro227His)
19g.44908898C>GCA406304356APOEc.602C>G (p.Pro201Arg)
c.680C>G (p.Pro227Arg)
19g.44908898C>TCA406304357APOEc.602C>T (p.Pro201Leu)
c.680C>T (p.Pro227Leu)
gnomAD v4
19g.44908899C>ACA507947420APOEc.603C>A (p.Pro201=)
c.681C>A (p.Pro227=)
gnomAD v4
19g.44908899C=CA2338167953APOEc.603C= (p.Pro201=)
c.681C= (p.Pro227=)
19g.44908899C>GCA507947421APOEc.603C>G (p.Pro201=)
c.681C>G (p.Pro227=)
19g.44908899C>TCA507947422APOEc.603C>T (p.Pro201=)
c.681C>T (p.Pro227=)
dbSNP gnomAD v4
19g.44908900C>ACA406304359APOEc.604C>A (p.Leu202Met)
c.682C>A (p.Leu228Met)
19g.44908900C>GCA406304360APOEc.604C>G (p.Leu202Val)
c.682C>G (p.Leu228Val)
19g.44908900C>TCA507947423APOEc.604C>T (p.Leu202=)
c.682C>T (p.Leu228=)
19g.44908901T>ACA406304361APOEc.605T>A (p.Leu202Gln)
c.683T>A (p.Leu228Gln)
19g.44908901T>CCA406304362APOEc.605T>C (p.Leu202Pro)
c.683T>C (p.Leu228Pro)
19g.44908901T>GCA406304364APOEc.605T>G (p.Leu202Arg)
c.683T>G (p.Leu228Arg)
19g.44908902G>ACA507947426APOEc.606G>A (p.Leu202=)
c.684G>A (p.Leu228=)
dbSNP gnomAD v3 gnomAD v4
19g.44908902G>CCA507947428APOEc.606G>C (p.Leu202=)
c.684G>C (p.Leu228=)
19g.44908902G=CA2338167954APOEc.606G= (p.Leu202=)
c.684G= (p.Leu228=)
19g.44908902G>TCA507947429APOEc.606G>T (p.Leu202=)
c.684G>T (p.Leu228=)
gnomAD v4
19g.44908903G>ACA406304366APOEc.607G>A (p.Val203Met)
c.685G>A (p.Val229Met)
19g.44908903G>CCA406304367APOEc.607G>C (p.Val203Leu)
c.685G>C (p.Val229Leu)
gnomAD v4
19g.44908903G>TCA406304368APOEc.607G>T (p.Val203Leu)
c.685G>T (p.Val229Leu)
gnomAD v4
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)

Number of alleles fetched