Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.116790700G>ACA382738219APOA5c.529C>T (p.Gln177Ter)
c.613C>T (p.Gln205Ter)
 gnomAD v4
11g.116790700G>CCA382738220APOA5c.529C>G (p.Gln177Glu)
c.613C>G (p.Gln205Glu)
11g.116790700G=CA2002740789APOA5c.529C= (p.Gln177=)
c.613C= (p.Gln205=)
11g.116790700G>TCA6289060APOA5c.529C>A (p.Gln177Lys)
c.613C>A (p.Gln205Lys)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790701C>ACA477047872APOA5c.528G>T (p.Leu176=)
c.612G>T (p.Leu204=)
11g.116790701C>GCA477047874APOA5c.528G>C (p.Leu176=)
c.612G>C (p.Leu204=)
11g.116790701C>TCA477047875APOA5c.528G>A (p.Leu176=)
c.612G>A (p.Leu204=)
 gnomAD v4
11g.116790702A>CCA382738221APOA5c.527T>G (p.Leu176Arg)
c.611T>G (p.Leu204Arg)
11g.116790702A>GCA382738222APOA5c.527T>C (p.Leu176Pro)
c.611T>C (p.Leu204Pro)
11g.116790702A>TCA382738223APOA5c.527T>A (p.Leu176Gln)
c.611T>A (p.Leu204Gln)
11g.116790703G>ACA477047878APOA5c.526C>T (p.Leu176=)
c.610C>T (p.Leu204=)
 gnomAD v4
11g.116790703G>CCA382738224APOA5c.526C>G (p.Leu176Val)
c.610C>G (p.Leu204Val)
11g.116790703G>TCA382738225APOA5c.526C>A (p.Leu176Met)
c.610C>A (p.Leu204Met)
11g.116790704T>ACA477047881APOA5c.525A>T (p.Gly175=)
c.609A>T (p.Gly203=)
11g.116790704T>CCA477047882APOA5c.525A>G (p.Gly175=)
c.609A>G (p.Gly203=)
11g.116790704T>GCA477047883APOA5c.525A>C (p.Gly175=)
c.609A>C (p.Gly203=)
 gnomAD v4
11g.116790705C>ACA382738226APOA5c.524G>T (p.Gly175Val)
c.608G>T (p.Gly203Val)
11g.116790705C=CA2002740790APOA5c.524G= (p.Gly175=)
c.608G= (p.Gly203=)
11g.116790705C>GCA6289061APOA5c.524G>C (p.Gly175Ala)
c.608G>C (p.Gly203Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790705C>TCA382738227APOA5c.524G>A (p.Gly175Glu)
c.608G>A (p.Gly203Glu)
11g.116790706C>ACA382738228APOA5c.523G>T (p.Gly175Ter)
c.607G>T (p.Gly203Ter)
11g.116790706C>GCA382738229APOA5c.523G>C (p.Gly175Arg)
c.607G>C (p.Gly203Arg)
11g.116790706C>TCA382738230APOA5c.523G>A (p.Gly175Arg)
c.607G>A (p.Gly203Arg)
 gnomAD v4
11g.116790707C>ACA382738231APOA5c.522G>T (p.Gln174His)
c.606G>T (p.Gln202His)
11g.116790707C>GCA382738232APOA5c.522G>C (p.Gln174His)
c.606G>C (p.Gln202His)
11g.116790707C>TCA477047889APOA5c.522G>A (p.Gln174=)
c.606G>A (p.Gln202=)
11g.116790708T>ACA382738233APOA5c.521A>T (p.Gln174Leu)
c.605A>T (p.Gln202Leu)
11g.116790708T>CCA6289062APOA5c.521A>G (p.Gln174Arg)
c.605A>G (p.Gln202Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790708T>GCA382738234APOA5c.521A>C (p.Gln174Pro)
c.605A>C (p.Gln202Pro)
 dbSNP
11g.116790708T=CA2002740793APOA5c.521A= (p.Gln174=)
c.605A= (p.Gln202=)
11g.116790709G>ACA382738235APOA5c.520C>T (p.Gln174Ter)
c.604C>T (p.Gln202Ter)
11g.116790709G>CCA382738236APOA5c.520C>G (p.Gln174Glu)
c.604C>G (p.Gln202Glu)
 gnomAD v4
11g.116790709G>TCA382738237APOA5c.520C>A (p.Gln174Lys)
c.604C>A (p.Gln202Lys)
11g.116790710C>ACA477047895APOA5c.519G>T (p.Leu173=)
c.603G>T (p.Leu201=)
 dbSNP gnomAD v2 gnomAD v4
11g.116790710C=CA2002740800APOA5c.519G= (p.Leu173=)
c.603G= (p.Leu201=)
11g.116790710C>GCA477047896APOA5c.519G>C (p.Leu173=)
c.603G>C (p.Leu201=)
11g.116790710C>TCA6289063APOA5c.519G>A (p.Leu173=)
c.603G>A (p.Leu201=)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790711A=CA2002740802APOA5c.518T= (p.Leu173=)
c.602T= (p.Leu201=)
11g.116790711A>CCA382738238APOA5c.518T>G (p.Leu173Arg)
c.602T>G (p.Leu201Arg)
 dbSNP gnomAD v4
11g.116790711A>GCA6289064APOA5c.518T>C (p.Leu173Pro)
c.602T>C (p.Leu201Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790711A>TCA382738239APOA5c.518T>A (p.Leu173Gln)
c.602T>A (p.Leu201Gln)
11g.116790712G>ACA477047898APOA5c.517C>T (p.Leu173=)
c.601C>T (p.Leu201=)
11g.116790712G>CCA382738240APOA5c.517C>G (p.Leu173Val)
c.601C>G (p.Leu201Val)
11g.116790712G>TCA382738241APOA5c.517C>A (p.Leu173Met)
c.601C>A (p.Leu201Met)
 gnomAD v4
11g.116790713C>ACA382738242APOA5c.516G>T (p.Leu172Phe)
c.600G>T (p.Leu200Phe)
11g.116790713C>GCA382738243APOA5c.516G>C (p.Leu172Phe)
c.600G>C (p.Leu200Phe)
11g.116790713C>TCA477047904APOA5c.516G>A (p.Leu172=)
c.600G>A (p.Leu200=)
11g.116790714A>CCA382738244APOA5c.515T>G (p.Leu172Trp)
c.599T>G (p.Leu200Trp)
11g.116790714A>GCA382738245APOA5c.515T>C (p.Leu172Ser)
c.599T>C (p.Leu200Ser)
11g.116790714A>TCA382738248APOA5c.515T>A (p.Leu172Ter)
c.599T>A (p.Leu200Ter)
11g.116790715A>CCA382738249APOA5c.514T>G (p.Leu172Val)
c.598T>G (p.Leu200Val)
11g.116790715A>GCA477047909APOA5c.514T>C (p.Leu172=)
c.598T>C (p.Leu200=)
11g.116790715A>TCA382738250APOA5c.514T>A (p.Leu172Met)
c.598T>A (p.Leu200Met)
11g.116790720_116790725delCA2697558959APOA5c.509_514del (p.Trp170_Ala171del)
c.593_598del (p.Trp198_Ala199del)
 ClinVar
11g.116790716A>CCA477047910APOA5c.513T>G (p.Ala171=)
c.597T>G (p.Ala199=)
11g.116790716A>GCA477047912APOA5c.513T>C (p.Ala171=)
c.597T>C (p.Ala199=)
11g.116790716A>TCA477047913APOA5c.513T>A (p.Ala171=)
c.597T>A (p.Ala199=)
11g.116790717G>ACA382738251APOA5c.512C>T (p.Ala171Val)
c.596C>T (p.Ala199Val)
 COSMIC
11g.116790717G>CCA382738252APOA5c.512C>G (p.Ala171Gly)
c.596C>G (p.Ala199Gly)
11g.116790717G>TCA382738253APOA5c.512C>A (p.Ala171Asp)
c.596C>A (p.Ala199Asp)
 gnomAD v4 COSMIC
11g.116790718C>ACA382738255APOA5c.511G>T (p.Ala171Ser)
c.595G>T (p.Ala199Ser)
11g.116790718C=CA2002740806APOA5c.511G= (p.Ala171=)
c.595G= (p.Ala199=)
11g.116790718C>GCA382738254APOA5c.511G>C (p.Ala171Pro)
c.595G>C (p.Ala199Pro)
11g.116790718C>TCA6289065APOA5c.511G>A (p.Ala171Thr)
c.595G>A (p.Ala199Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790719C>ACA382738256APOA5c.510G>T (p.Trp170Cys)
c.594G>T (p.Trp198Cys)
11g.116790719C>GCA382738257APOA5c.510G>C (p.Trp170Cys)
c.594G>C (p.Trp198Cys)
11g.116790719C>TCA382738258APOA5c.510G>A (p.Trp170Ter)
c.594G>A (p.Trp198Ter)
11g.116790720C>ACA382738259APOA5c.509G>T (p.Trp170Leu)
c.593G>T (p.Trp198Leu)
11g.116790720C>GCA382738260APOA5c.509G>C (p.Trp170Ser)
c.593G>C (p.Trp198Ser)
11g.116790720C>TCA382738261APOA5c.509G>A (p.Trp170Ter)
c.593G>A (p.Trp198Ter)
11g.116790721A>CCA382738262APOA5c.508T>G (p.Trp170Gly)
c.592T>G (p.Trp198Gly)
11g.116790721A>GCA382738263APOA5c.508T>C (p.Trp170Arg)
c.592T>C (p.Trp198Arg)
 dbSNP
11g.116790721A>TCA382738264APOA5c.508T>A (p.Trp170Arg)
c.592T>A (p.Trp198Arg)
11g.116790722A>CCA477047923APOA5c.507T>G (p.Ala169=)
c.591T>G (p.Ala197=)
 dbSNP
11g.116790722A>GCA477047925APOA5c.507T>C (p.Ala169=)
c.591T>C (p.Ala197=)
11g.116790722A>TCA477047926APOA5c.507T>A (p.Ala169=)
c.591T>A (p.Ala197=)
 dbSNP
11g.116790723G>ACA382738265APOA5c.506C>T (p.Ala169Val)
c.590C>T (p.Ala197Val)
11g.116790723G>CCA382738266APOA5c.506C>G (p.Ala169Gly)
c.590C>G (p.Ala197Gly)
11g.116790723G>TCA382738267APOA5c.506C>A (p.Ala169Asp)
c.590C>A (p.Ala197Asp)
11g.116790724C>ACA382738268APOA5c.505G>T (p.Ala169Ser)
c.589G>T (p.Ala197Ser)
 dbSNP gnomAD v3 gnomAD v4
11g.116790724C=CA2002740807APOA5c.505G= (p.Ala169=)
c.589G= (p.Ala197=)
11g.116790724C>GCA382738270APOA5c.505G>C (p.Ala169Pro)
c.589G>C (p.Ala197Pro)
11g.116790724C>TCA382738269APOA5c.505G>A (p.Ala169Thr)
c.589G>A (p.Ala197Thr)
11g.116790725C>ACA382738271APOA5c.504G>T (p.Glu168Asp)
c.588G>T (p.Glu196Asp)
11g.116790725C=CA2002740811APOA5c.504G= (p.Glu168=)
c.588G= (p.Glu196=)
11g.116790725C>GCA6289067APOA5c.504G>C (p.Glu168Asp)
c.588G>C (p.Glu196Asp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790725C>TCA6289066APOA5c.504G>A (p.Glu168=)
c.588G>A (p.Glu196=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790726T>ACA382738272APOA5c.503A>T (p.Glu168Val)
c.587A>T (p.Glu196Val)
11g.116790726T>CCA382738273APOA5c.503A>G (p.Glu168Gly)
c.587A>G (p.Glu196Gly)
11g.116790726T>GCA382738274APOA5c.503A>C (p.Glu168Ala)
c.587A>C (p.Glu196Ala)
11g.116790727C>ACA382738275APOA5c.502G>T (p.Glu168Ter)
c.586G>T (p.Glu196Ter)
 gnomAD v4
11g.116790727C>GCA382738276APOA5c.502G>C (p.Glu168Gln)
c.586G>C (p.Glu196Gln)
11g.116790727C>TCA382738277APOA5c.502G>A (p.Glu168Lys)
c.586G>A (p.Glu196Lys)
 COSMIC
11g.116790728G>ACA477047936APOA5c.501C>T (p.Asp167=)
c.585C>T (p.Asp195=)
 gnomAD v4 COSMIC
11g.116790728G>CCA382738278APOA5c.501C>G (p.Asp167Glu)
c.585C>G (p.Asp195Glu)
 dbSNP
11g.116790728G=CA2002740814APOA5c.501C= (p.Asp167=)
c.585C= (p.Asp195=)
11g.116790728G>TCA382738279APOA5c.501C>A (p.Asp167Glu)
c.585C>A (p.Asp195Glu)
 gnomAD v4
11g.116790729T>ACA6289068APOA5c.500A>T (p.Asp167Val)
c.584A>T (p.Asp195Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790729T>CCA382738280APOA5c.500A>G (p.Asp167Gly)
c.584A>G (p.Asp195Gly)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116790729T>GCA382738281APOA5c.500A>C (p.Asp167Ala)
c.584A>C (p.Asp195Ala)
11g.116790729T=CA2002740816APOA5c.500A= (p.Asp167=)
c.584A= (p.Asp195=)
11g.116790730C>ACA382738284APOA5c.499G>T (p.Asp167Tyr)
c.583G>T (p.Asp195Tyr)
11g.116790730C>GCA382738283APOA5c.499G>C (p.Asp167His)
c.583G>C (p.Asp195His)
 gnomAD v4
11g.116790730C>TCA382738282APOA5c.499G>A (p.Asp167Asn)
c.583G>A (p.Asp195Asn)
11g.116790731C>ACA477047942APOA5c.498G>T (p.Val166=)
c.582G>T (p.Val194=)
11g.116790731C>GCA477047943APOA5c.498G>C (p.Val166=)
c.582G>C (p.Val194=)
11g.116790731C>TCA477047945APOA5c.498G>A (p.Val166=)
c.582G>A (p.Val194=)
11g.116790732A>CCA382738285APOA5c.497T>G (p.Val166Gly)
c.581T>G (p.Val194Gly)
11g.116790732A>GCA382738286APOA5c.497T>C (p.Val166Ala)
c.581T>C (p.Val194Ala)
11g.116790732A>TCA382738287APOA5c.497T>A (p.Val166Glu)
c.581T>A (p.Val194Glu)
11g.116790733C>ACA382738288APOA5c.496G>T (p.Val166Leu)
c.580G>T (p.Val194Leu)
11g.116790733C=CA2002740820APOA5c.496G= (p.Val166=)
c.580G= (p.Val194=)
11g.116790733C>GCA382738289APOA5c.496G>C (p.Val166Leu)
c.580G>C (p.Val194Leu)
11g.116790733C>TCA382738290APOA5c.496G>A (p.Val166Met)
c.580G>A (p.Val194Met)
 dbSNP gnomAD v2 gnomAD v4
11g.116790734G>ACA477047951APOA5c.495C>T (p.Gly165=)
c.579C>T (p.Gly193=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116790734G>CCA477047952APOA5c.495C>G (p.Gly165=)
c.579C>G (p.Gly193=)
11g.116790734G=CA2002740822APOA5c.495C= (p.Gly165=)
c.579C= (p.Gly193=)
11g.116790734G>TCA6289069APOA5c.495C>A (p.Gly165=)
c.579C>A (p.Gly193=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790735C>ACA382738291APOA5c.494G>T (p.Gly165Val)
c.578G>T (p.Gly193Val)
11g.116790735C=CA2002740830APOA5c.494G= (p.Gly165=)
c.578G= (p.Gly193=)
11g.116790735C>GCA382738292APOA5c.494G>C (p.Gly165Ala)
c.578G>C (p.Gly193Ala)
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.116790735C>TCA382738293APOA5c.494G>A (p.Gly165Asp)
c.578G>A (p.Gly193Asp)
 dbSNP gnomAD v2
11g.116790740dupCA6289070APOA5c.494dup (p.Val166ArgfsTer?)
c.578dup (p.Val194ArgfsTer?)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790740delCA2616086364APOA5c.494del (p.Gly165AlafsTer?)
c.578del (p.Gly193AlafsTer?)
 gnomAD v4
11g.116790736C>ACA382738294APOA5c.493G>T (p.Gly165Cys)
c.577G>T (p.Gly193Cys)
11g.116790736C=CA2002740837APOA5c.493G= (p.Gly165=)
c.577G= (p.Gly193=)
11g.116790736C>GCA6289071APOA5c.493G>C (p.Gly165Arg)
c.577G>C (p.Gly193Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790736C>TCA382738295APOA5c.493G>A (p.Gly165Ser)
c.577G>A (p.Gly193Ser)
 gnomAD v4
11g.116790737C>ACA477047967APOA5c.492G>T (p.Gly164=)
c.576G>T (p.Gly192=)
11g.116790737C=CA2002740839APOA5c.492G= (p.Gly164=)
c.576G= (p.Gly192=)
11g.116790737C>GCA477047968APOA5c.492G>C (p.Gly164=)
c.576G>C (p.Gly192=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116790737C>TCA477047969APOA5c.492G>A (p.Gly164=)
c.576G>A (p.Gly192=)
 dbSNP gnomAD v2 gnomAD v4
11g.116790738C>ACA382738297APOA5c.491G>T (p.Gly164Val)
c.575G>T (p.Gly192Val)
11g.116790738C>GCA382738298APOA5c.491G>C (p.Gly164Ala)
c.575G>C (p.Gly192Ala)
11g.116790738C>TCA382738296APOA5c.491G>A (p.Gly164Glu)
c.575G>A (p.Gly192Glu)
11g.116790739C>ACA382738299APOA5c.490G>T (p.Gly164Trp)
c.574G>T (p.Gly192Trp)
11g.116790739C=CA2002740844APOA5c.490G= (p.Gly164=)
c.574G= (p.Gly192=)
11g.116790739C>GCA6289073APOA5c.490G>C (p.Gly164Arg)
c.574G>C (p.Gly192Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790739C>TCA6289072APOA5c.490G>A (p.Gly164Arg)
c.574G>A (p.Gly192Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790740C>ACA477047979APOA5c.489G>T (p.Leu163=)
c.573G>T (p.Leu191=)
11g.116790740C>GCA477047980APOA5c.489G>C (p.Leu163=)
c.573G>C (p.Leu191=)
11g.116790740C>TCA477047981APOA5c.489G>A (p.Leu163=)
c.573G>A (p.Leu191=)
11g.116790741A=CA2002740850APOA5c.488T= (p.Leu163=)
c.572T= (p.Leu191=)
11g.116790741A>CCA382738300APOA5c.488T>G (p.Leu163Arg)
c.572T>G (p.Leu191Arg)
 dbSNP
11g.116790741A>GCA382738301APOA5c.488T>C (p.Leu163Pro)
c.572T>C (p.Leu191Pro)
11g.116790741A>TCA382738302APOA5c.488T>A (p.Leu163Gln)
c.572T>A (p.Leu191Gln)
11g.116790742G>ACA477047985APOA5c.487C>T (p.Leu163=)
c.571C>T (p.Leu191=)
 gnomAD v4
11g.116790742G>CCA382738303APOA5c.487C>G (p.Leu163Val)
c.571C>G (p.Leu191Val)
11g.116790742G>TCA382738304APOA5c.487C>A (p.Leu163Met)
c.571C>A (p.Leu191Met)
11g.116790743C>ACA382738305APOA5c.486G>T (p.Leu162Phe)
c.570G>T (p.Leu190Phe)
11g.116790743C>GCA382738306APOA5c.486G>C (p.Leu162Phe)
c.570G>C (p.Leu190Phe)
11g.116790743C>TCA477047988APOA5c.486G>A (p.Leu162=)
c.570G>A (p.Leu190=)
11g.116790744A=CA2002740854APOA5c.485T= (p.Leu162=)
c.569T= (p.Leu190=)
11g.116790744A>CCA382738307APOA5c.485T>G (p.Leu162Trp)
c.569T>G (p.Leu190Trp)
 dbSNP gnomAD v3 gnomAD v4
11g.116790744A>GCA382738308APOA5c.485T>C (p.Leu162Ser)
c.569T>C (p.Leu190Ser)
11g.116790744A>TCA382738309APOA5c.485T>A (p.Leu162Ter)
c.569T>A (p.Leu190Ter)
11g.116790745A>CCA382738311APOA5c.484T>G (p.Leu162Val)
c.568T>G (p.Leu190Val)
11g.116790745A>GCA477047993APOA5c.484T>C (p.Leu162=)
c.568T>C (p.Leu190=)
 dbSNP gnomAD v4
11g.116790745A>TCA382738310APOA5c.484T>A (p.Leu162Met)
c.568T>A (p.Leu190Met)
 gnomAD v4
11g.116790746C>ACA382738312APOA5c.483G>T (p.Gln161His)
c.567G>T (p.Gln189His)
 COSMIC
11g.116790746C>GCA382738313APOA5c.483G>C (p.Gln161His)
c.567G>C (p.Gln189His)
11g.116790746C>TCA477047995APOA5c.483G>A (p.Gln161=)
c.567G>A (p.Gln189=)
11g.116790747T>ACA382738314APOA5c.482A>T (p.Gln161Leu)
c.566A>T (p.Gln189Leu)
11g.116790747T>CCA382738315APOA5c.482A>G (p.Gln161Arg)
c.566A>G (p.Gln189Arg)
11g.116790747T>GCA382738316APOA5c.482A>C (p.Gln161Pro)
c.566A>C (p.Gln189Pro)
11g.116790748G>ACA382738317APOA5c.481C>T (p.Gln161Ter)
c.565C>T (p.Gln189Ter)
11g.116790748G>CCA382738318APOA5c.481C>G (p.Gln161Glu)
c.565C>G (p.Gln189Glu)
11g.116790748G>TCA382738319APOA5c.481C>A (p.Gln161Lys)
c.565C>A (p.Gln189Lys)
11g.116790749G>ACA6289074APOA5c.480C>T (p.Ala160=)
c.564C>T (p.Ala188=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790749G>CCA477047999APOA5c.480C>G (p.Ala160=)
c.564C>G (p.Ala188=)
11g.116790749G=CA2002740856APOA5c.480C= (p.Ala160=)
c.564C= (p.Ala188=)
11g.116790749G>TCA477047997APOA5c.480C>A (p.Ala160=)
c.564C>A (p.Ala188=)
 ClinVar gnomAD v4
11g.116790750G>ACA382738320APOA5c.479C>T (p.Ala160Val)
c.563C>T (p.Ala188Val)
 gnomAD v4
11g.116790750G>CCA382738321APOA5c.479C>G (p.Ala160Gly)
c.563C>G (p.Ala188Gly)
11g.116790750G>TCA382738322APOA5c.479C>A (p.Ala160Asp)
c.563C>A (p.Ala188Asp)
 gnomAD v4
11g.116790751C>ACA382738323APOA5c.478G>T (p.Ala160Ser)
c.562G>T (p.Ala188Ser)
11g.116790751C=CA2002740858APOA5c.478G= (p.Ala160=)
c.562G= (p.Ala188=)
11g.116790751C>GCA382738325APOA5c.478G>C (p.Ala160Pro)
c.562G>C (p.Ala188Pro)
11g.116790751C>TCA382738324APOA5c.478G>A (p.Ala160Thr)
c.562G>A (p.Ala188Thr)
 dbSNP
11g.116790752C>ACA382738326APOA5c.477G>T (p.Lys159Asn)
c.561G>T (p.Lys187Asn)
11g.116790752C=CA2002740860APOA5c.477G= (p.Lys159=)
c.561G= (p.Lys187=)
11g.116790752C>GCA382738327APOA5c.477G>C (p.Lys159Asn)
c.561G>C (p.Lys187Asn)
11g.116790752C>TCA477048013APOA5c.477G>A (p.Lys159=)
c.561G>A (p.Lys187=)
 dbSNP gnomAD v3 gnomAD v4
11g.116790753T>ACA382738328APOA5c.476A>T (p.Lys159Met)
c.560A>T (p.Lys187Met)
11g.116790753T>CCA382738329APOA5c.476A>G (p.Lys159Arg)
c.560A>G (p.Lys187Arg)
 dbSNP
11g.116790753T>GCA382738330APOA5c.476A>C (p.Lys159Thr)
c.560A>C (p.Lys187Thr)
11g.116790753T=CA2002740862APOA5c.476A= (p.Lys159=)
c.560A= (p.Lys187=)
11g.116790754T>ACA382738331APOA5c.475A>T (p.Lys159Ter)
c.559A>T (p.Lys187Ter)
11g.116790754T>CCA382738332APOA5c.475A>G (p.Lys159Glu)
c.559A>G (p.Lys187Glu)
11g.116790754T>GCA382738333APOA5c.475A>C (p.Lys159Gln)
c.559A>C (p.Lys187Gln)
11g.116790755G>ACA477048018APOA5c.474C>T (p.Thr158=)
c.558C>T (p.Thr186=)
 dbSNP gnomAD v4
11g.116790755G>CCA477048019APOA5c.474C>G (p.Thr158=)
c.558C>G (p.Thr186=)
 dbSNP gnomAD v2
11g.116790755G=CA2002740865APOA5c.474C= (p.Thr158=)
c.558C= (p.Thr186=)
11g.116790755G>TCA477048016APOA5c.474C>A (p.Thr158=)
c.558C>A (p.Thr186=)
11g.116790756G>ACA382738334APOA5c.473C>T (p.Thr158Ile)
c.557C>T (p.Thr186Ile)
 gnomAD v4
11g.116790756G>CCA382738335APOA5c.473C>G (p.Thr158Ser)
c.557C>G (p.Thr186Ser)
11g.116790756G>TCA382738336APOA5c.473C>A (p.Thr158Asn)
c.557C>A (p.Thr186Asn)
 gnomAD v4
11g.116790757T>ACA382738337APOA5c.472A>T (p.Thr158Ser)
c.556A>T (p.Thr186Ser)
11g.116790757T>CCA382738338APOA5c.472A>G (p.Thr158Ala)
c.556A>G (p.Thr186Ala)
11g.116790757T>GCA382738339APOA5c.472A>C (p.Thr158Pro)
c.556A>C (p.Thr186Pro)
 dbSNP
11g.116790757T=CA2002740868APOA5c.472A= (p.Thr158=)
c.556A= (p.Thr186=)
11g.116790758G>ACA477048030APOA5c.471C>T (p.Asp157=)
c.555C>T (p.Asp185=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.116790758G>CCA382738340APOA5c.471C>G (p.Asp157Glu)
c.555C>G (p.Asp185Glu)
11g.116790758G=CA2002740872APOA5c.471C= (p.Asp157=)
c.555C= (p.Asp185=)
11g.116790758G>TCA382738341APOA5c.471C>A (p.Asp157Glu)
c.555C>A (p.Asp185Glu)
 gnomAD v4
11g.116790759T>ACA382738342APOA5c.470A>T (p.Asp157Val)
c.554A>T (p.Asp185Val)
11g.116790759T>CCA382738343APOA5c.470A>G (p.Asp157Gly)
c.554A>G (p.Asp185Gly)
11g.116790759T>GCA382738344APOA5c.470A>C (p.Asp157Ala)
c.554A>C (p.Asp185Ala)
11g.116790760C>ACA382738345APOA5c.469G>T (p.Asp157Tyr)
c.553G>T (p.Asp185Tyr)
11g.116790760C>GCA382738346APOA5c.469G>C (p.Asp157His)
c.553G>C (p.Asp185His)
11g.116790760C>TCA382738347APOA5c.469G>A (p.Asp157Asn)
c.553G>A (p.Asp185Asn)
11g.116790761T>ACA382738348APOA5c.468A>T (p.Glu156Asp)
c.552A>T (p.Glu184Asp)
11g.116790761T>CCA477048038APOA5c.468A>G (p.Glu156=)
c.552A>G (p.Glu184=)
 dbSNP
11g.116790761T>GCA382738349APOA5c.468A>C (p.Glu156Asp)
c.552A>C (p.Glu184Asp)
11g.116790761T=CA2002740874APOA5c.468A= (p.Glu156=)
c.552A= (p.Glu184=)
11g.116790761_116790790delinsTTCCCCCACCACGCGCAACTGCTCCTGCAGCA2002740875APOA5c.439_468delinsCTGCAGGAGCAGTTGCGCGTGGTGGGGGAA (p.Leu147=)
c.523_552delinsCTGCAGGAGCAGTTGCGCGTGGTGGGGGAA (p.Leu175=)
11g.116790762T>ACA382738350APOA5c.467A>T (p.Glu156Val)
c.551A>T (p.Glu184Val)
11g.116790762T>CCA382738351APOA5c.467A>G (p.Glu156Gly)
c.551A>G (p.Glu184Gly)
11g.116790762T>GCA382738352APOA5c.467A>C (p.Glu156Ala)
c.551A>C (p.Glu184Ala)
11g.116790762_116790790delCA2002740876APOA5c.439_467del (p.Leu147ArgfsTer?)
c.523_551del (p.Leu175ArgfsTer?)
 dbSNP
11g.116790763C>ACA6289075APOA5c.466G>T (p.Glu156Ter)
c.550G>T (p.Glu184Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790763C=CA2002740879APOA5c.466G= (p.Glu156=)
c.550G= (p.Glu184=)
11g.116790763C>GCA382738354APOA5c.466G>C (p.Glu156Gln)
c.550G>C (p.Glu184Gln)
11g.116790763C>TCA382738353APOA5c.466G>A (p.Glu156Lys)
c.550G>A (p.Glu184Lys)
 dbSNP gnomAD v4 COSMIC
11g.116790767delCA645571761APOA5c.466del (p.Glu156LysfsTer?)
c.550del (p.Glu184LysfsTer?)
 gnomAD v4 COSMIC
11g.116790764C>ACA477047457APOA5c.465G>T (p.Gly155=)
c.549G>T (p.Gly183=)
11g.116790764C=CA2002740884APOA5c.465G= (p.Gly155=)
c.549G= (p.Gly183=)
11g.116790764C>GCA477047455APOA5c.465G>C (p.Gly155=)
c.549G>C (p.Gly183=)
11g.116790764C>TCA477047453APOA5c.465G>A (p.Gly155=)
c.549G>A (p.Gly183=)
 ClinVar dbSNP
11g.116790765C>ACA382738355APOA5c.464G>T (p.Gly155Val)
c.548G>T (p.Gly183Val)
 gnomAD v4
11g.116790765C>GCA382738356APOA5c.464G>C (p.Gly155Ala)
c.548G>C (p.Gly183Ala)
11g.116790765C>TCA382738357APOA5c.464G>A (p.Gly155Glu)
c.548G>A (p.Gly183Glu)
 ClinVar gnomAD v4
11g.116790766_116790772dupCA2616086397APOA5c.458_464dup (p.Glu156GlyfsTer?)
c.542_548dup (p.Glu184GlyfsTer?)
 gnomAD v4
11g.116790766C>ACA382738358APOA5c.463G>T (p.Gly155Trp)
c.547G>T (p.Gly183Trp)
11g.116790766C>GCA382738359APOA5c.463G>C (p.Gly155Arg)
c.547G>C (p.Gly183Arg)
 gnomAD v4
11g.116790766C>TCA382738360APOA5c.463G>A (p.Gly155Arg)
c.547G>A (p.Gly183Arg)
11g.116790767C>ACA477047459APOA5c.462G>T (p.Val154=)
c.546G>T (p.Val182=)
11g.116790767C>GCA477047461APOA5c.462G>C (p.Val154=)
c.546G>C (p.Val182=)
11g.116790767C>TCA477047460APOA5c.462G>A (p.Val154=)
c.546G>A (p.Val182=)
11g.116790768A>CCA382738361APOA5c.461T>G (p.Val154Gly)
c.545T>G (p.Val182Gly)
11g.116790768A>GCA382738362APOA5c.461T>C (p.Val154Ala)
c.545T>C (p.Val182Ala)
11g.116790768A>TCA382738363APOA5c.461T>A (p.Val154Glu)
c.545T>A (p.Val182Glu)
11g.116790769C>ACA382738364APOA5c.460G>T (p.Val154Leu)
c.544G>T (p.Val182Leu)
11g.116790769C=CA2002740887APOA5c.460G= (p.Val154=)
c.544G= (p.Val182=)
11g.116790769C>GCA382738365APOA5c.460G>C (p.Val154Leu)
c.544G>C (p.Val182Leu)
 dbSNP gnomAD v3 gnomAD v4
11g.116790769C>TCA229337938APOA5c.460G>A (p.Val154Met)
c.544G>A (p.Val182Met)
 dbSNP gnomAD v2 gnomAD v4
11g.116790770C>ACA477047465APOA5c.459G>T (p.Val153=)
c.543G>T (p.Val181=)
11g.116790770C=CA2002740889APOA5c.459G= (p.Val153=)
c.543G= (p.Val181=)
11g.116790770C>GCA477047467APOA5c.459G>C (p.Val153=)
c.543G>C (p.Val181=)
 ClinVar dbSNP gnomAD v4
11g.116790770C>TCA477047469APOA5c.459G>A (p.Val153=)
c.543G>A (p.Val181=)
11g.116790771A>CCA382738367APOA5c.458T>G (p.Val153Gly)
c.542T>G (p.Val181Gly)
11g.116790771A>GCA382738368APOA5c.458T>C (p.Val153Ala)
c.542T>C (p.Val181Ala)
11g.116790771A>TCA382738366APOA5c.458T>A (p.Val153Glu)
c.542T>A (p.Val181Glu)
11g.116790772C>ACA382738369APOA5c.457G>T (p.Val153Leu)
c.541G>T (p.Val181Leu)
11g.116790772C=CA1630855369APOA5c.457G= (p.Val153=)
c.541G= (p.Val181=)
11g.116790772C>GCA382738370APOA5c.457G>C (p.Val153Leu)
c.541G>C (p.Val181Leu)
 gnomAD v4
11g.116790772C>TCA6289076APOA5c.457G>A (p.Val153Met)
c.541G>A (p.Val181Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790773G>ACA477047474APOA5c.456C>T (p.Arg152=)
c.540C>T (p.Arg180=)
 dbSNP gnomAD v4
11g.116790773G>CCA477047475APOA5c.456C>G (p.Arg152=)
c.540C>G (p.Arg180=)
 gnomAD v4
11g.116790773G=CA2002740897APOA5c.456C= (p.Arg152=)
c.540C= (p.Arg180=)
11g.116790773G>TCA229337944APOA5c.456C>A (p.Arg152=)
c.540C>A (p.Arg180=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116790774C>ACA382738371APOA5c.455G>T (p.Arg152Leu)
c.539G>T (p.Arg180Leu)
 gnomAD v4
11g.116790774C=CA2002740904APOA5c.455G= (p.Arg152=)
c.539G= (p.Arg180=)
11g.116790774C>GCA382738372APOA5c.455G>C (p.Arg152Pro)
c.539G>C (p.Arg180Pro)
11g.116790774C>TCA6289077APOA5c.455G>A (p.Arg152His)
c.539G>A (p.Arg180His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.116790775G>ACA229337960APOA5c.454C>T (p.Arg152Cys)
c.538C>T (p.Arg180Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116790775G>CCA382738374APOA5c.454C>G (p.Arg152Gly)
c.538C>G (p.Arg180Gly)
11g.116790775G=CA2002740908APOA5c.454C= (p.Arg152=)
c.538C= (p.Arg180=)
11g.116790775G>TCA382738373APOA5c.454C>A (p.Arg152Ser)
c.538C>A (p.Arg180Ser)
 dbSNP gnomAD v2 gnomAD v4
11g.116790776C>ACA382738375APOA5c.453G>T (p.Leu151Phe)
c.537G>T (p.Leu179Phe)
11g.116790776C>GCA382738376APOA5c.453G>C (p.Leu151Phe)
c.537G>C (p.Leu179Phe)
11g.116790776C>TCA477047481APOA5c.453G>A (p.Leu151=)
c.537G>A (p.Leu179=)
11g.116790777A>CCA382738377APOA5c.452T>G (p.Leu151Trp)
c.536T>G (p.Leu179Trp)
11g.116790777A>GCA382738378APOA5c.452T>C (p.Leu151Ser)
c.536T>C (p.Leu179Ser)
 gnomAD v4
11g.116790777A>TCA382738379APOA5c.452T>A (p.Leu151Ter)
c.536T>A (p.Leu179Ter)
11g.116790778A>CCA382738381APOA5c.451T>G (p.Leu151Val)
c.535T>G (p.Leu179Val)
11g.116790778A>GCA477047485APOA5c.451T>C (p.Leu151=)
c.535T>C (p.Leu179=)
 COSMIC
11g.116790778A>TCA382738380APOA5c.451T>A (p.Leu151Met)
c.535T>A (p.Leu179Met)
11g.116790779C>ACA382738382APOA5c.450G>T (p.Gln150His)
c.534G>T (p.Gln178His)
11g.116790779C>GCA382738383APOA5c.450G>C (p.Gln150His)
c.534G>C (p.Gln178His)
11g.116790779C>TCA477047487APOA5c.450G>A (p.Gln150=)
c.534G>A (p.Gln178=)
11g.116790779_116790782delCA2695215434APOA5c.447_450del (p.Glu149AspfsTer?)
c.531_534del (p.Glu177AspfsTer?)
11g.116790780T>ACA382738384APOA5c.449A>T (p.Gln150Leu)
c.533A>T (p.Gln178Leu)
11g.116790780T>CCA382738385APOA5c.449A>G (p.Gln150Arg)
c.533A>G (p.Gln178Arg)
11g.116790780T>GCA382738386APOA5c.449A>C (p.Gln150Pro)
c.533A>C (p.Gln178Pro)
11g.116790780T=CA2002740914APOA5c.449A= (p.Gln150=)
c.533A= (p.Gln178=)
11g.116790781G>ACA382738387APOA5c.448C>T (p.Gln150Ter)
c.532C>T (p.Gln178Ter)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116790781G>CCA382738388APOA5c.448C>G (p.Gln150Glu)
c.532C>G (p.Gln178Glu)
11g.116790781G=CA2002740917APOA5c.448C= (p.Gln150=)
c.532C= (p.Gln178=)
11g.116790781G>TCA382738389APOA5c.448C>A (p.Gln150Lys)
c.532C>A (p.Gln178Lys)
 gnomAD v4
11g.116790790_116790798dupCA942583221APOA5c.440_448dup (p.Glu149_Gln150insLeuGlnGlu)
c.524_532dup (p.Glu177_Gln178insLeuGlnGlu)
 dbSNP gnomAD v3 gnomAD v4
11g.116790781_116790782insGACA2616086424APOA5c.447_448insTC (p.Gln150SerfsTer?)
c.531_532insTC (p.Gln178SerfsTer?)
 gnomAD v4
11g.116790782C>ACA382738390APOA5c.447G>T (p.Glu149Asp)
c.531G>T (p.Glu177Asp)
11g.116790782C=CA2002740923APOA5c.447G= (p.Glu149=)
c.531G= (p.Glu177=)
11g.116790782C>GCA382738391APOA5c.447G>C (p.Glu149Asp)
c.531G>C (p.Glu177Asp)
 gnomAD v4
11g.116790782C>TCA477047494APOA5c.447G>A (p.Glu149=)
c.531G>A (p.Glu177=)
 dbSNP gnomAD v2 gnomAD v4
11g.116790782delinsGAGCA2695215435APOA5c.447delinsCTC (p.Glu149AspfsTer?)
c.531delinsCTC (p.Glu177AspfsTer?)
11g.116790783T>ACA382738392APOA5c.446A>T (p.Glu149Val)
c.530A>T (p.Glu177Val)
11g.116790783T>CCA382738393APOA5c.446A>G (p.Glu149Gly)
c.530A>G (p.Glu177Gly)
11g.116790783T>GCA382738394APOA5c.446A>C (p.Glu149Ala)
c.530A>C (p.Glu177Ala)
 dbSNP gnomAD v2 gnomAD v4
11g.116790783T=CA2002740927APOA5c.446A= (p.Glu149=)
c.530A= (p.Glu177=)
11g.116790784C>ACA382738395APOA5c.445G>T (p.Glu149Ter)
c.529G>T (p.Glu177Ter)
11g.116790784C>GCA382738396APOA5c.445G>C (p.Glu149Gln)
c.529G>C (p.Glu177Gln)
11g.116790784C>TCA382738397APOA5c.445G>A (p.Glu149Lys)
c.529G>A (p.Glu177Lys)
 COSMIC
11g.116790785C>ACA382738398APOA5c.444G>T (p.Gln148His)
c.528G>T (p.Gln176His)
11g.116790785C=CA2002740930APOA5c.444G= (p.Gln148=)
c.528G= (p.Gln176=)
11g.116790785C>GCA382738399APOA5c.444G>C (p.Gln148His)
c.528G>C (p.Gln176His)
11g.116790785C>TCA477047497APOA5c.444G>A (p.Gln148=)
c.528G>A (p.Gln176=)
 dbSNP gnomAD v2 gnomAD v4
11g.116790786T>ACA382738400APOA5c.443A>T (p.Gln148Leu)
c.527A>T (p.Gln176Leu)
11g.116790786T>CCA382738401APOA5c.443A>G (p.Gln148Arg)
c.527A>G (p.Gln176Arg)
11g.116790786T>GCA382738402APOA5c.443A>C (p.Gln148Pro)
c.527A>C (p.Gln176Pro)
11g.116790787G>ACA382738403APOA5c.442C>T (p.Gln148Ter)
c.526C>T (p.Gln176Ter)
11g.116790787G>CCA382738404APOA5c.442C>G (p.Gln148Glu)
c.526C>G (p.Gln176Glu)
11g.116790787G>TCA382738405APOA5c.442C>A (p.Gln148Lys)
c.526C>A (p.Gln176Lys)
 gnomAD v4
11g.116790788C>ACA477047500APOA5c.441G>T (p.Leu147=)
c.525G>T (p.Leu175=)
11g.116790788C>GCA477047503APOA5c.441G>C (p.Leu147=)
c.525G>C (p.Leu175=)
11g.116790788C>TCA477047501APOA5c.441G>A (p.Leu147=)
c.525G>A (p.Leu175=)
11g.116790789A>CCA382738406APOA5c.440T>G (p.Leu147Arg)
c.524T>G (p.Leu175Arg)
11g.116790789A>GCA382738407APOA5c.440T>C (p.Leu147Pro)
c.524T>C (p.Leu175Pro)
11g.116790789A>TCA382738408APOA5c.440T>A (p.Leu147Gln)
c.524T>A (p.Leu175Gln)
11g.116790789_116790799delinsAGCTCCTGCACCA2002740933APOA5c.430_440delinsGTGCAGGAGCT (p.Val144=)
c.514_524delinsGTGCAGGAGCT (p.Val172=)
11g.116790790G>ACA477047507APOA5c.439C>T (p.Leu147=)
c.523C>T (p.Leu175=)
11g.116790790G>CCA382738409APOA5c.439C>G (p.Leu147Val)
c.523C>G (p.Leu175Val)
11g.116790790G>TCA382738410APOA5c.439C>A (p.Leu147Met)
c.523C>A (p.Leu175Met)
11g.116790792_116790801delCA2002740935APOA5c.430_439del (p.Val144CysfsTer?)
c.514_523del (p.Val172CysfsTer?)
 dbSNP
11g.116790791C>ACA6289078APOA5c.438G>T (p.Glu146Asp)
c.522G>T (p.Glu174Asp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790791C=CA2002740936APOA5c.438G= (p.Glu146=)
c.522G= (p.Glu174=)
11g.116790791C>GCA382738411APOA5c.438G>C (p.Glu146Asp)
c.522G>C (p.Glu174Asp)
11g.116790791C>TCA477047516APOA5c.438G>A (p.Glu146=)
c.522G>A (p.Glu174=)
11g.116790792T>ACA382738414APOA5c.437A>T (p.Glu146Val)
c.521A>T (p.Glu174Val)
11g.116790792T>CCA382738412APOA5c.437A>G (p.Glu146Gly)
c.521A>G (p.Glu174Gly)
11g.116790792T>GCA382738413APOA5c.437A>C (p.Glu146Ala)
c.521A>C (p.Glu174Ala)
11g.116790792_116790793delinsTCCA2002740939APOA5c.436_437delinsGA (p.Glu146=)
c.520_521delinsGA (p.Glu174=)
11g.116790793C>ACA382738415APOA5c.436G>T (p.Glu146Ter)
c.520G>T (p.Glu174Ter)
11g.116790793C>GCA382738416APOA5c.436G>C (p.Glu146Gln)
c.520G>C (p.Glu174Gln)
11g.116790793C>TCA382738417APOA5c.436G>A (p.Glu146Lys)
c.520G>A (p.Glu174Lys)
11g.116790794delCA2002740941APOA5c.436del (p.Glu146SerfsTer?)
c.520del (p.Glu174SerfsTer?)
 dbSNP
11g.116790794C>ACA382738418APOA5c.435G>T (p.Gln145His)
c.519G>T (p.Gln173His)
11g.116790794C=CA2002740945APOA5c.435G= (p.Gln145=)
c.519G= (p.Gln173=)
11g.116790794C>GCA382738419APOA5c.435G>C (p.Gln145His)
c.519G>C (p.Gln173His)
11g.116790794C>TCA477047524APOA5c.435G>A (p.Gln145=)
c.519G>A (p.Gln173=)
 dbSNP
11g.116790795T>ACA382738421APOA5c.434A>T (p.Gln145Leu)
c.518A>T (p.Gln173Leu)
11g.116790795T>CCA6289079APOA5c.434A>G (p.Gln145Arg)
c.518A>G (p.Gln173Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790795T>GCA382738420APOA5c.434A>C (p.Gln145Pro)
c.518A>C (p.Gln173Pro)
11g.116790795T=CA2002740949APOA5c.434A= (p.Gln145=)
c.518A= (p.Gln173=)
11g.116790796G>ACA382738422APOA5c.433C>T (p.Gln145Ter)
c.517C>T (p.Gln173Ter)
 COSMIC
11g.116790796G>CCA382738423APOA5c.433C>G (p.Gln145Glu)
c.517C>G (p.Gln173Glu)
11g.116790796G>TCA382738424APOA5c.433C>A (p.Gln145Lys)
c.517C>A (p.Gln173Lys)
11g.116790797C>ACA477047534APOA5c.432G>T (p.Val144=)
c.516G>T (p.Val172=)
 dbSNP
11g.116790797C=CA2002740951APOA5c.432G= (p.Val144=)
c.516G= (p.Val172=)
11g.116790797C>GCA477047530APOA5c.432G>C (p.Val144=)
c.516G>C (p.Val172=)
11g.116790797C>TCA477047532APOA5c.432G>A (p.Val144=)
c.516G>A (p.Val172=)
 dbSNP gnomAD v3 gnomAD v4
11g.116790798A>CCA382738425APOA5c.431T>G (p.Val144Gly)
c.515T>G (p.Val172Gly)
 dbSNP
11g.116790798A>GCA382738426APOA5c.431T>C (p.Val144Ala)
c.515T>C (p.Val172Ala)
11g.116790798A>TCA382738427APOA5c.431T>A (p.Val144Glu)
c.515T>A (p.Val172Glu)
11g.116790799C>ACA382738429APOA5c.430G>T (p.Val144Leu)
c.514G>T (p.Val172Leu)
11g.116790799C=CA2002740955APOA5c.430G= (p.Val144=)
c.514G= (p.Val172=)
11g.116790799C>GCA382738428APOA5c.430G>C (p.Val144Leu)
c.514G>C (p.Val172Leu)
 gnomAD v4
11g.116790799C>TCA6289080APOA5c.430G>A (p.Val144Met)
c.514G>A (p.Val172Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790800G>ACA6289081APOA5c.429C>T (p.Arg143=)
c.513C>T (p.Arg171=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790800G>CCA477047539APOA5c.429C>G (p.Arg143=)
c.513C>G (p.Arg171=)
11g.116790800G=CA2002740958APOA5c.429C= (p.Arg143=)
c.513C= (p.Arg171=)
11g.116790800G>TCA477047541APOA5c.429C>A (p.Arg143=)
c.513C>A (p.Arg171=)

Number of alleles fetched