Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908683G>ACA308885459APOEc.387G>A (p.Val129=)
c.465G>A (p.Val155=)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.44908683G>CCA507947527APOEc.387G>C (p.Val129=)
c.465G>C (p.Val155=)
19g.44908683G=CA2338167525APOEc.387G= (p.Val129=)
c.465G= (p.Val155=)
19g.44908683G>TCA507947525APOEc.387G>T (p.Val129=)
c.465G>T (p.Val155=)
19g.44908684T>ACA406303927APOEc.388T>A (p.Cys130Ser)
c.466T>A (p.Cys156Ser)
19g.44908684T>CCA127512APOEc.388T>C (p.Cys130Arg)
c.466T>C (p.Cys156Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.[44908684T>C;44908774C>T]CA041161APOEc.[388T>C;478C>T] (p.[Cys130Arg;Arg160Cys])
c.[466T>C;556C>T] (p.[Cys156Arg;Arg186Cys])
ClinVar
19g.[44908684T>C;44909101C>G]CA041740APOEc.[388T>C;805C>G] (p.[Cys130Arg;Arg269Gly])
c.[466T>C;883C>G] (p.[Cys156Arg;Arg295Gly])
ClinVar
19g.44908684T>GCA406303928APOEc.388T>G (p.Cys130Gly)
c.466T>G (p.Cys156Gly)
19g.44908684T=CA2338167530APOEc.388T= (p.Cys130=)
c.466T= (p.Cys156=)
19g.44908685G>ACA406303929APOEc.389G>A (p.Cys130Tyr)
c.467G>A (p.Cys156Tyr)
dbSNP gnomAD v2 gnomAD v4
19g.44908685G>CCA406303930APOEc.389G>C (p.Cys130Ser)
c.467G>C (p.Cys156Ser)
19g.44908685G=CA2338167534APOEc.389G= (p.Cys130=)
c.467G= (p.Cys156=)
19g.44908685G>TCA406303931APOEc.389G>T (p.Cys130Phe)
c.467G>T (p.Cys156Phe)
19g.44908687_44908692delCA2585715438APOEc.391_396del (p.Gly131_Arg132del)
c.469_474del (p.Gly157_Arg158del)
gnomAD v4
19g.44908686C>ACA406303932APOEc.390C>A (p.Cys130Ter)
c.468C>A (p.Cys156Ter)
19g.44908686C>GCA406303933APOEc.390C>G (p.Cys130Trp)
c.468C>G (p.Cys156Trp)
19g.44908686C>TCA507947534APOEc.390C>T (p.Cys130=)
c.468C>T (p.Cys156=)
gnomAD v4
19g.44908687G>ACA406303936APOEc.391G>A (p.Gly131Ser)
c.469G>A (p.Gly157Ser)
dbSNP gnomAD v2 gnomAD v4 COSMIC
19g.44908687G>CCA406303935APOEc.391G>C (p.Gly131Arg)
c.469G>C (p.Gly157Arg)
19g.44908687G=CA2338167537APOEc.391G= (p.Gly131=)
c.469G= (p.Gly157=)
19g.44908687G>TCA406303934APOEc.391G>T (p.Gly131Cys)
c.469G>T (p.Gly157Cys)
dbSNP gnomAD v2 gnomAD v4
19g.44908688G>ACA406303937APOEc.392G>A (p.Gly131Asp)
c.470G>A (p.Gly157Asp)
dbSNP gnomAD v4
19g.44908688G>CCA406303938APOEc.392G>C (p.Gly131Ala)
c.470G>C (p.Gly157Ala)
19g.44908688G=CA2338167542APOEc.392G= (p.Gly131=)
c.470G= (p.Gly157=)
19g.44908688G>TCA406303939APOEc.392G>T (p.Gly131Val)
c.470G>T (p.Gly157Val)
gnomAD v4
19g.44908689C>ACA507947538APOEc.393C>A (p.Gly131=)
c.471C>A (p.Gly157=)
19g.44908689C>GCA507947542APOEc.393C>G (p.Gly131=)
c.471C>G (p.Gly157=)
19g.44908689C>TCA507947539APOEc.393C>T (p.Gly131=)
c.471C>T (p.Gly157=)
19g.44908690C>ACA308885481APOEc.394C>A (p.Arg132Ser)
c.472C>A (p.Arg158Ser)
dbSNP
19g.44908690C=CA2338167546APOEc.394C= (p.Arg132=)
c.472C= (p.Arg158=)
19g.44908690C>GCA406303940APOEc.394C>G (p.Arg132Gly)
c.472C>G (p.Arg158Gly)
19g.44908690C>TCA9506055APOEc.394C>T (p.Arg132Cys)
c.472C>T (p.Arg158Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908691G>ACA406303941APOEc.395G>A (p.Arg132His)
c.473G>A (p.Arg158His)
dbSNP gnomAD v4
19g.44908691G>CCA406303942APOEc.395G>C (p.Arg132Pro)
c.473G>C (p.Arg158Pro)
19g.44908691G=CA2338167548APOEc.395G= (p.Arg132=)
c.473G= (p.Arg158=)
19g.44908691G>TCA406303943APOEc.395G>T (p.Arg132Leu)
c.473G>T (p.Arg158Leu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908692C>ACA507947546APOEc.396C>A (p.Arg132=)
c.474C>A (p.Arg158=)
19g.44908692C>GCA507947547APOEc.396C>G (p.Arg132=)
c.474C>G (p.Arg158=)
19g.44908692C>TCA507947548APOEc.396C>T (p.Arg132=)
c.474C>T (p.Arg158=)
19g.44908693C>ACA406303944APOEc.397C>A (p.Leu133Met)
c.475C>A (p.Leu159Met)
19g.44908693C=CA2338167549APOEc.397C= (p.Leu133=)
c.475C= (p.Leu159=)
19g.44908693C>GCA406303945APOEc.397C>G (p.Leu133Val)
c.475C>G (p.Leu159Val)
19g.44908693C>TCA507947549APOEc.397C>T (p.Leu133=)
c.475C>T (p.Leu159=)
dbSNP gnomAD v4
19g.44908694T>ACA406303948APOEc.398T>A (p.Leu133Gln)
c.476T>A (p.Leu159Gln)
19g.44908694T>CCA406303947APOEc.398T>C (p.Leu133Pro)
c.476T>C (p.Leu159Pro)
19g.44908694T>GCA406303946APOEc.398T>G (p.Leu133Arg)
c.476T>G (p.Leu159Arg)
gnomAD v4
19g.44908695G>ACA507947555APOEc.399G>A (p.Leu133=)
c.477G>A (p.Leu159=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44908695G>CCA507947556APOEc.399G>C (p.Leu133=)
c.477G>C (p.Leu159=)
19g.44908695G=CA2338167553APOEc.399G= (p.Leu133=)
c.477G= (p.Leu159=)

Number of alleles fetched