Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)
19g.44907821G>TCA406302498APOEc.105G>T (p.Gln35His)
c.183G>T (p.Gln61His)
gnomAD v4
19g.44907822A>CCA406302499APOEc.106A>C (p.Thr36Pro)
c.184A>C (p.Thr62Pro)
19g.44907822A>GCA406302500APOEc.106A>G (p.Thr36Ala)
c.184A>G (p.Thr62Ala)
dbSNP gnomAD v4
19g.44907822A>TCA406302501APOEc.106A>T (p.Thr36Ser)
c.184A>T (p.Thr62Ser)
19g.44907823C>ACA406302504APOEc.107C>A (p.Thr36Asn)
c.185C>A (p.Thr62Asn)
19g.44907823C>GCA406302503APOEc.107C>G (p.Thr36Ser)
c.185C>G (p.Thr62Ser)
19g.44907823C>TCA406302502APOEc.107C>T (p.Thr36Ile)
c.185C>T (p.Thr62Ile)
19g.44907824C>ACA507798996APOEc.108C>A (p.Thr36=)
c.186C>A (p.Thr62=)
gnomAD v4
19g.44907824C=CA2338167340APOEc.108C= (p.Thr36=)
c.186C= (p.Thr62=)
19g.44907824C>GCA9505977APOEc.108C>G (p.Thr36=)
c.186C>G (p.Thr62=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.44907824C>TCA9505976APOEc.108C>T (p.Thr36=)
c.186C>T (p.Thr62=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.44907825G>ACA9505978APOEc.109G>A (p.Glu37Lys)
c.187G>A (p.Glu63Lys)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.44907825G>CCA406303180APOEc.109G>C (p.Glu37Gln)
c.187G>C (p.Glu63Gln)
19g.44907825G=CA2338167341APOEc.109G= (p.Glu37=)
c.187G= (p.Glu63=)
19g.44907825G>TCA406303182APOEc.109G>T (p.Glu37Ter)
c.187G>T (p.Glu63Ter)
19g.44907826A>CCA406303184APOEc.110A>C (p.Glu37Ala)
c.188A>C (p.Glu63Ala)
19g.44907826A>GCA406303189APOEc.110A>G (p.Glu37Gly)
c.188A>G (p.Glu63Gly)
19g.44907826A>TCA406303192APOEc.110A>T (p.Glu37Val)
c.188A>T (p.Glu63Val)
19g.44907827G>ACA507799001APOEc.111G>A (p.Glu37=)
c.189G>A (p.Glu63=)
19g.44907827G>CCA406303198APOEc.111G>C (p.Glu37Asp)
c.189G>C (p.Glu63Asp)
19g.44907827G>TCA406303200APOEc.111G>T (p.Glu37Asp)
c.189G>T (p.Glu63Asp)
19g.44907828T>ACA406303204APOEc.112T>A (p.Trp38Arg)
c.190T>A (p.Trp64Arg)
19g.44907828T>CCA406303207APOEc.112T>C (p.Trp38Arg)
c.190T>C (p.Trp64Arg)
19g.44907828T>GCA406303209APOEc.112T>G (p.Trp38Gly)
c.190T>G (p.Trp64Gly)
19g.44907829G>ACA406303218APOEc.113G>A (p.Trp38Ter)
c.191G>A (p.Trp64Ter)
19g.44907829G>CCA406303222APOEc.113G>C (p.Trp38Ser)
c.191G>C (p.Trp64Ser)
19g.44907829G=CA2338167342APOEc.113G= (p.Trp38=)
c.191G= (p.Trp64=)
19g.44907829G>TCA406303216APOEc.113G>T (p.Trp38Leu)
c.191G>T (p.Trp64Leu)
dbSNP gnomAD v3 gnomAD v4
19g.44907830G>ACA406303231APOEc.114G>A (p.Trp38Ter)
c.192G>A (p.Trp64Ter)
ClinVar dbSNP
19g.44907830G>CCA406303226APOEc.114G>C (p.Trp38Cys)
c.192G>C (p.Trp64Cys)
19g.44907830G=CA2740130013APOEc.114G= (p.Trp38=)
c.192G= (p.Trp64=)
19g.44907830G>TCA406303228APOEc.114G>T (p.Trp38Cys)
c.192G>T (p.Trp64Cys)
19g.44907831C>ACA406303234APOEc.115C>A (p.Gln39Lys)
c.193C>A (p.Gln65Lys)
19g.44907831C>GCA406303239APOEc.115C>G (p.Gln39Glu)
c.193C>G (p.Gln65Glu)
19g.44907831C>TCA406303240APOEc.115C>T (p.Gln39Ter)
c.193C>T (p.Gln65Ter)
gnomAD v4
19g.44907832A=CA2338167343APOEc.116A= (p.Gln39=)
c.194A= (p.Gln65=)
19g.44907832A>CCA406303242APOEc.116A>C (p.Gln39Pro)
c.194A>C (p.Gln65Pro)
19g.44907832A>GCA9505979APOEc.116A>G (p.Gln39Arg)
c.194A>G (p.Gln65Arg)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC

Number of alleles fetched