Chr Mutation (hg38) CAid Gene Transcript Linkouts
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=)

Number of alleles fetched