Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44907807G>ACA041327APOEc.91G>A (p.Glu31Lys)
c.169G>A (p.Glu57Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.[44907807G>A;44908783C>T]CA041334APOEc.[91G>A;487C>T] (p.[Glu31Lys;Arg163Cys])
c.[169G>A;565C>T] (p.[Glu57Lys;Arg189Cys])
ClinVar
19g.44907807G>CCA406302466APOEc.91G>C (p.Glu31Gln)
c.169G>C (p.Glu57Gln)
19g.44907807G=CA2338167335APOEc.91G= (p.Glu31=)
c.169G= (p.Glu57=)
19g.44907807G>TCA406302467APOEc.91G>T (p.Glu31Ter)
c.169G>T (p.Glu57Ter)
19g.44907808A>CCA406302468APOEc.92A>C (p.Glu31Ala)
c.170A>C (p.Glu57Ala)
19g.44907808A>GCA406302469APOEc.92A>G (p.Glu31Gly)
c.170A>G (p.Glu57Gly)
19g.44907808A>TCA406302470APOEc.92A>T (p.Glu31Val)
c.170A>T (p.Glu57Val)
19g.44907809G>ACA507798986APOEc.93G>A (p.Glu31=)
c.171G>A (p.Glu57=)
19g.44907809G>CCA406302471APOEc.93G>C (p.Glu31Asp)
c.171G>C (p.Glu57Asp)
19g.44907809G>TCA406302472APOEc.93G>T (p.Glu31Asp)
c.171G>T (p.Glu57Asp)
19g.44907810C>ACA406302473APOEc.94C>A (p.Leu32Met)
c.172C>A (p.Leu58Met)
19g.44907810C>GCA406302474APOEc.94C>G (p.Leu32Val)
c.172C>G (p.Leu58Val)
19g.44907810C>TCA507798987APOEc.94C>T (p.Leu32=)
c.172C>T (p.Leu58=)
gnomAD v4
19g.44907811T>ACA406302477APOEc.95T>A (p.Leu32Gln)
c.173T>A (p.Leu58Gln)
19g.44907811T>CCA406302476APOEc.95T>C (p.Leu32Pro)
c.173T>C (p.Leu58Pro)
19g.44907811T>GCA406302475APOEc.95T>G (p.Leu32Arg)
c.173T>G (p.Leu58Arg)
19g.44907812G>ACA507798988APOEc.96G>A (p.Leu32=)
c.174G>A (p.Leu58=)
19g.44907812G>CCA507798989APOEc.96G>C (p.Leu32=)
c.174G>C (p.Leu58=)
19g.44907812G>TCA507798990APOEc.96G>T (p.Leu32=)
c.174G>T (p.Leu58=)
19g.44907813C>ACA406302478APOEc.97C>A (p.Arg33Ser)
c.175C>A (p.Arg59Ser)
19g.44907813C=CA2338167336APOEc.97C= (p.Arg33=)
c.175C= (p.Arg59=)
19g.44907813C>GCA406302479APOEc.97C>G (p.Arg33Gly)
c.175C>G (p.Arg59Gly)
19g.44907813C>TCA9505975APOEc.97C>T (p.Arg33Cys)
c.175C>T (p.Arg59Cys)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44907814G>ACA406302480APOEc.98G>A (p.Arg33His)
c.176G>A (p.Arg59His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.44907814G>CCA406302481APOEc.98G>C (p.Arg33Pro)
c.176G>C (p.Arg59Pro)
19g.44907814G=CA2338167337APOEc.98G= (p.Arg33=)
c.176G= (p.Arg59=)
19g.44907814G>TCA406302482APOEc.98G>T (p.Arg33Leu)
c.176G>T (p.Arg59Leu)
gnomAD v4
19g.44907815C>ACA507798991APOEc.99C>A (p.Arg33=)
c.177C>A (p.Arg59=)
19g.44907815C>GCA507798993APOEc.99C>G (p.Arg33=)
c.177C>G (p.Arg59=)
19g.44907815C>TCA507798992APOEc.99C>T (p.Arg33=)
c.177C>T (p.Arg59=)
19g.44907816C>ACA406302483APOEc.100C>A (p.Gln34Lys)
c.178C>A (p.Gln60Lys)
19g.44907816C=CA2338167338APOEc.100C= (p.Gln34=)
c.178C= (p.Gln60=)
19g.44907816C>GCA406302484APOEc.100C>G (p.Gln34Glu)
c.178C>G (p.Gln60Glu)
19g.44907816C>TCA406302485APOEc.100C>T (p.Gln34Ter)
c.178C>T (p.Gln60Ter)
dbSNP gnomAD v4
19g.44907817A>CCA406302486APOEc.101A>C (p.Gln34Pro)
c.179A>C (p.Gln60Pro)
gnomAD v4
19g.44907817A>GCA406302487APOEc.101A>G (p.Gln34Arg)
c.179A>G (p.Gln60Arg)
19g.44907817A>TCA406302488APOEc.101A>T (p.Gln34Leu)
c.179A>T (p.Gln60Leu)
19g.44907818G>ACA507798994APOEc.102G>A (p.Gln34=)
c.180G>A (p.Gln60=)
19g.44907818G>CCA406302489APOEc.102G>C (p.Gln34His)
c.180G>C (p.Gln60His)
19g.44907818G>TCA406302490APOEc.102G>T (p.Gln34His)
c.180G>T (p.Gln60His)
dbSNP gnomAD v4
19g.44907819C>ACA406302491APOEc.103C>A (p.Gln35Lys)
c.181C>A (p.Gln61Lys)
19g.44907819C>GCA406302492APOEc.103C>G (p.Gln35Glu)
c.181C>G (p.Gln61Glu)
19g.44907819C>TCA406302493APOEc.103C>T (p.Gln35Ter)
c.181C>T (p.Gln61Ter)
19g.44907820A=CA2338167339APOEc.104A= (p.Gln35=)
c.182A= (p.Gln61=)
19g.44907820A>CCA406302494APOEc.104A>C (p.Gln35Pro)
c.182A>C (p.Gln61Pro)
gnomAD v4
19g.44907820A>GCA406302495APOEc.104A>G (p.Gln35Arg)
c.182A>G (p.Gln61Arg)
dbSNP gnomAD v2 gnomAD v4
19g.44907820A>TCA406302496APOEc.104A>T (p.Gln35Leu)
c.182A>T (p.Gln61Leu)
dbSNP
19g.44907821G>ACA507798995APOEc.105G>A (p.Gln35=)
c.183G>A (p.Gln61=)
gnomAD v4
19g.44907821G>CCA406302497APOEc.105G>C (p.Gln35His)
c.183G>C (p.Gln61His)

Number of alleles fetched