Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.44908734G>ACA507947653APOEc.438G>A (p.Gln146=)
c.516G>A (p.Gln172=)
gnomAD v4
19g.44908734G>CCA406304026APOEc.438G>C (p.Gln146His)
c.516G>C (p.Gln172His)
19g.44908734G>TCA406304027APOEc.438G>T (p.Gln146His)
c.516G>T (p.Gln172His)
gnomAD v4
19g.44908737_44908743dupCA882663992APOEc.441_447dup (p.Glu150HisfsTer17)
c.519_525dup (p.Glu176HisfsTer17)
dbSNP
19g.44908735A>CCA406304028APOEc.439A>C (p.Ser147Arg)
c.517A>C (p.Ser173Arg)
19g.44908735A>GCA406304029APOEc.439A>G (p.Ser147Gly)
c.517A>G (p.Ser173Gly)
19g.44908735A>TCA406304030APOEc.439A>T (p.Ser147Cys)
c.517A>T (p.Ser173Cys)
19g.44908736G>ACA406304031APOEc.440G>A (p.Ser147Asn)
c.518G>A (p.Ser173Asn)
gnomAD v4 COSMIC
19g.44908736G>CCA406304032APOEc.440G>C (p.Ser147Thr)
c.518G>C (p.Ser173Thr)
gnomAD v4
19g.44908736G>TCA406304033APOEc.440G>T (p.Ser147Ile)
c.518G>T (p.Ser173Ile)
gnomAD v4
19g.44908737C>ACA406304034APOEc.441C>A (p.Ser147Arg)
c.519C>A (p.Ser173Arg)
gnomAD v4
19g.44908737C=CA2338167667APOEc.441C= (p.Ser147=)
c.519C= (p.Ser173=)
19g.44908737C>GCA406304035APOEc.441C>G (p.Ser147Arg)
c.519C>G (p.Ser173Arg)
19g.44908737C>TCA507947662APOEc.441C>T (p.Ser147=)
c.519C>T (p.Ser173=)
dbSNP gnomAD v2 gnomAD v4
19g.44908738A>CCA406304036APOEc.442A>C (p.Thr148Pro)
c.520A>C (p.Thr174Pro)
19g.44908738A>GCA406304037APOEc.442A>G (p.Thr148Ala)
c.520A>G (p.Thr174Ala)
19g.44908738A>TCA406304038APOEc.442A>T (p.Thr148Ser)
c.520A>T (p.Thr174Ser)
19g.44908739C>ACA406304040APOEc.443C>A (p.Thr148Asn)
c.521C>A (p.Thr174Asn)
19g.44908739C=CA2338167671APOEc.443C= (p.Thr148=)
c.521C= (p.Thr174=)
19g.44908739C>GCA406304039APOEc.443C>G (p.Thr148Ser)
c.521C>G (p.Thr174Ser)
19g.44908739C>TCA308885618APOEc.443C>T (p.Thr148Ile)
c.521C>T (p.Thr174Ile)
dbSNP gnomAD v4
19g.44908740C>ACA507947665APOEc.444C>A (p.Thr148=)
c.522C>A (p.Thr174=)
dbSNP gnomAD v2 gnomAD v4
19g.44908740C=CA2338167673APOEc.444C= (p.Thr148=)
c.522C= (p.Thr174=)
19g.44908740C>GCA9506066APOEc.444C>G (p.Thr148=)
c.522C>G (p.Thr174=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.44908740C>TCA507947664APOEc.444C>T (p.Thr148=)
c.522C>T (p.Thr174=)
dbSNP gnomAD v4 COSMIC
19g.44908741G>ACA406304041APOEc.445G>A (p.Glu149Lys)
c.523G>A (p.Glu175Lys)
dbSNP gnomAD v2 gnomAD v4
19g.44908741G>CCA406304042APOEc.445G>C (p.Glu149Gln)
c.523G>C (p.Glu175Gln)
gnomAD v4
19g.44908741G=CA2338167679APOEc.445G= (p.Glu149=)
c.523G= (p.Glu175=)
19g.44908741G>TCA406304043APOEc.445G>T (p.Glu149Ter)
c.523G>T (p.Glu175Ter)
gnomAD v4
19g.44908756_44908757insTCTGGGAAGGGCTGGGCAGCAGAGGAGCTGCGGGTGCCA9506067APOEc.460_461insTCTGGGAAGGGCTGGGCAGCAGAGGAGCTGCGGGTGC (p.Arg154LeufsTer23)
c.538_539insTCTGGGAAGGGCTGGGCAGCAGAGGAGCTGCGGGTGC (p.Arg180LeufsTer23)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44908742A>CCA406304044APOEc.446A>C (p.Glu149Ala)
c.524A>C (p.Glu175Ala)
19g.44908742A>GCA406304045APOEc.446A>G (p.Glu149Gly)
c.524A>G (p.Glu175Gly)
gnomAD v4
19g.44908742A>TCA406304046APOEc.446A>T (p.Glu149Val)
c.524A>T (p.Glu175Val)
19g.44908743G>ACA507947668APOEc.447G>A (p.Glu149=)
c.525G>A (p.Glu175=)
gnomAD v4
19g.44908743G>CCA9506068APOEc.447G>C (p.Glu149Asp)
c.525G>C (p.Glu175Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44908743G=CA2338167684APOEc.447G= (p.Glu149=)
c.525G= (p.Glu175=)
19g.44908743G>TCA406304047APOEc.447G>T (p.Glu149Asp)
c.525G>T (p.Glu175Asp)
gnomAD v4
19g.44908744G>ACA406304048APOEc.448G>A (p.Glu150Lys)
c.526G>A (p.Glu176Lys)
gnomAD v4
19g.44908744G>CCA406304049APOEc.448G>C (p.Glu150Gln)
c.526G>C (p.Glu176Gln)
19g.44908744G>TCA406304050APOEc.448G>T (p.Glu150Ter)
c.526G>T (p.Glu176Ter)
gnomAD v4
19g.44908745A=CA2338167686APOEc.449A= (p.Glu150=)
c.527A= (p.Glu176=)
19g.44908745A>CCA406304052APOEc.449A>C (p.Glu150Ala)
c.527A>C (p.Glu176Ala)
19g.44908745A>GCA308885645APOEc.449A>G (p.Glu150Gly)
c.527A>G (p.Glu176Gly)
dbSNP gnomAD v4
19g.44908745A>TCA406304051APOEc.449A>T (p.Glu150Val)
c.527A>T (p.Glu176Val)
19g.44908746G>ACA507947679APOEc.450G>A (p.Glu150=)
c.528G>A (p.Glu176=)
gnomAD v4
19g.44908746G>CCA406304053APOEc.450G>C (p.Glu150Asp)
c.528G>C (p.Glu176Asp)
19g.44908746G>TCA406304054APOEc.450G>T (p.Glu150Asp)
c.528G>T (p.Glu176Asp)
gnomAD v4
19g.44908747C>ACA345323APOEc.451C>A (p.Leu151Met)
c.529C>A (p.Leu177Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44908747C=CA2338167691APOEc.451C= (p.Leu151=)
c.529C= (p.Leu177=)
19g.44908747C>GCA406304055APOEc.451C>G (p.Leu151Val)
c.529C>G (p.Leu177Val)
gnomAD v4

Number of alleles fetched