Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.46894694G>ACA5970152LRP4c.1435C>T (p.Arg479Cys)
c.1648C>T (p.Arg550Cys)
c.631C>T (p.Arg211Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894694G>CCA380285537LRP4c.1435C>G (p.Arg479Gly)
c.1648C>G (p.Arg550Gly)
c.631C>G (p.Arg211Gly)
11g.46894694G=CA1969144823LRP4c.1435C= (p.Arg479=)
c.1648C= (p.Arg550=)
c.631C= (p.Arg211=)
11g.46894694G>TCA380285540LRP4c.1435C>A (p.Arg479Ser)
c.1648C>A (p.Arg550Ser)
c.631C>A (p.Arg211Ser)
11g.46894695G>ACA221647401LRP4c.1434C>T (p.Arg478=)
c.1647C>T (p.Arg549=)
c.630C>T (p.Arg210=)
 dbSNP gnomAD v3 gnomAD v4
11g.46894695G>CCA474204975LRP4c.1434C>G (p.Arg478=)
c.1647C>G (p.Arg549=)
c.630C>G (p.Arg210=)
11g.46894695G=CA1969144833LRP4c.1434C= (p.Arg478=)
c.1647C= (p.Arg549=)
c.630C= (p.Arg210=)
11g.46894695G>TCA474204976LRP4c.1434C>A (p.Arg478=)
c.1647C>A (p.Arg549=)
c.630C>A (p.Arg210=)
11g.46894696C>ACA380285543LRP4c.1433G>T (p.Arg478Leu)
c.1646G>T (p.Arg549Leu)
c.629G>T (p.Arg210Leu)
11g.46894696C=CA1969144836LRP4c.1433G= (p.Arg478=)
c.1646G= (p.Arg549=)
c.629G= (p.Arg210=)
11g.46894696C>GCA380285545LRP4c.1433G>C (p.Arg478Pro)
c.1646G>C (p.Arg549Pro)
c.629G>C (p.Arg210Pro)
11g.46894696C>TCA380285548LRP4c.1433G>A (p.Arg478His)
c.1646G>A (p.Arg549His)
c.629G>A (p.Arg210His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894697G>ACA5970153LRP4c.1432C>T (p.Arg478Cys)
c.1645C>T (p.Arg549Cys)
c.628C>T (p.Arg210Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894697G>CCA380285550LRP4c.1432C>G (p.Arg478Gly)
c.1645C>G (p.Arg549Gly)
c.628C>G (p.Arg210Gly)
11g.46894697G=CA1969144840LRP4c.1432C= (p.Arg478=)
c.1645C= (p.Arg549=)
c.628C= (p.Arg210=)
11g.46894697G>TCA380285552LRP4c.1432C>A (p.Arg478Ser)
c.1645C>A (p.Arg549Ser)
c.628C>A (p.Arg210Ser)
11g.46894698G>ACA474204977LRP4c.1431C>T (p.His477=)
c.1644C>T (p.His548=)
c.627C>T (p.His209=)
 gnomAD v4
11g.46894698G>CCA380285556LRP4c.1431C>G (p.His477Gln)
c.1644C>G (p.His548Gln)
c.627C>G (p.His209Gln)
11g.46894698G>TCA380285559LRP4c.1431C>A (p.His477Gln)
c.1644C>A (p.His548Gln)
c.627C>A (p.His209Gln)
11g.46894699T>ACA380285563LRP4c.1430A>T (p.His477Leu)
c.1643A>T (p.His548Leu)
c.626A>T (p.His209Leu)
11g.46894699T>CCA380285565LRP4c.1430A>G (p.His477Arg)
c.1643A>G (p.His548Arg)
c.626A>G (p.His209Arg)
11g.46894699T>GCA5970154LRP4c.1430A>C (p.His477Pro)
c.1643A>C (p.His548Pro)
c.626A>C (p.His209Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894699T=CA1969144844LRP4c.1430A= (p.His477=)
c.1643A= (p.His548=)
c.626A= (p.His209=)
11g.46894700G>ACA380285575LRP4c.1429C>T (p.His477Tyr)
c.1642C>T (p.His548Tyr)
c.625C>T (p.His209Tyr)
 COSMIC
11g.46894700G>CCA380285569LRP4c.1429C>G (p.His477Asp)
c.1642C>G (p.His548Asp)
c.625C>G (p.His209Asp)
11g.46894700G>TCA380285572LRP4c.1429C>A (p.His477Asn)
c.1642C>A (p.His548Asn)
c.625C>A (p.His209Asn)
11g.46894701G>ACA474204978LRP4c.1428C>T (p.His476=)
c.1641C>T (p.His547=)
c.624C>T (p.His208=)
11g.46894701G>CCA380285578LRP4c.1428C>G (p.His476Gln)
c.1641C>G (p.His547Gln)
c.624C>G (p.His208Gln)
11g.46894701G>TCA380285584LRP4c.1428C>A (p.His476Gln)
c.1641C>A (p.His547Gln)
c.624C>A (p.His208Gln)
11g.46894702T>ACA380285587LRP4c.1427A>T (p.His476Leu)
c.1640A>T (p.His547Leu)
c.623A>T (p.His208Leu)
11g.46894702T>CCA380285590LRP4c.1427A>G (p.His476Arg)
c.1640A>G (p.His547Arg)
c.623A>G (p.His208Arg)
11g.46894702T>GCA5970155LRP4c.1427A>C (p.His476Pro)
c.1640A>C (p.His547Pro)
c.623A>C (p.His208Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894702T=CA1969144850LRP4c.1427A= (p.His476=)
c.1640A= (p.His547=)
c.623A= (p.His208=)
11g.46894703G>ACA380285596LRP4c.1426C>T (p.His476Tyr)
c.1639C>T (p.His547Tyr)
c.622C>T (p.His208Tyr)
 dbSNP gnomAD v4
11g.46894703G>CCA380285599LRP4c.1426C>G (p.His476Asp)
c.1639C>G (p.His547Asp)
c.622C>G (p.His208Asp)
11g.46894703G=CA1969144854LRP4c.1426C= (p.His476=)
c.1639C= (p.His547=)
c.622C= (p.His208=)
11g.46894703G>TCA380285600LRP4c.1426C>A (p.His476Asn)
c.1639C>A (p.His547Asn)
c.622C>A (p.His208Asn)
11g.46894704G>ACA474204979LRP4c.1425C>T (p.Phe475=)
c.1638C>T (p.Phe546=)
c.621C>T (p.Phe207=)
11g.46894704G>CCA380285604LRP4c.1425C>G (p.Phe475Leu)
c.1638C>G (p.Phe546Leu)
c.621C>G (p.Phe207Leu)
11g.46894704G>TCA380285607LRP4c.1425C>A (p.Phe475Leu)
c.1638C>A (p.Phe546Leu)
c.621C>A (p.Phe207Leu)
11g.46894705A=CA1969144859LRP4c.1424T= (p.Phe475=)
c.1637T= (p.Phe546=)
c.620T= (p.Phe207=)
11g.46894705A>CCA380285611LRP4c.1424T>G (p.Phe475Cys)
c.1637T>G (p.Phe546Cys)
c.620T>G (p.Phe207Cys)
11g.46894705A>GCA5970156LRP4c.1424T>C (p.Phe475Ser)
c.1637T>C (p.Phe546Ser)
c.620T>C (p.Phe207Ser)
 dbSNP ExAC gnomAD v2
11g.46894705A>TCA380285614LRP4c.1424T>A (p.Phe475Tyr)
c.1637T>A (p.Phe546Tyr)
c.620T>A (p.Phe207Tyr)
11g.46894706A>CCA380285618LRP4c.1423T>G (p.Phe475Val)
c.1636T>G (p.Phe546Val)
c.619T>G (p.Phe207Val)
11g.46894706A>GCA380285625LRP4c.1423T>C (p.Phe475Leu)
c.1636T>C (p.Phe546Leu)
c.619T>C (p.Phe207Leu)
11g.46894706A>TCA380285621LRP4c.1423T>A (p.Phe475Ile)
c.1636T>A (p.Phe546Ile)
c.619T>A (p.Phe207Ile)
11g.46894707A>CCA380285629LRP4c.1422T>G (p.Asp474Glu)
c.1635T>G (p.Asp545Glu)
c.618T>G (p.Asp206Glu)
11g.46894707A>GCA474204980LRP4c.1422T>C (p.Asp474=)
c.1635T>C (p.Asp545=)
c.618T>C (p.Asp206=)
11g.46894707A>TCA380285631LRP4c.1422T>A (p.Asp474Glu)
c.1635T>A (p.Asp545Glu)
c.618T>A (p.Asp206Glu)
11g.46894708T>ACA380285634LRP4c.1421A>T (p.Asp474Val)
c.1634A>T (p.Asp545Val)
c.617A>T (p.Asp206Val)
11g.46894708T>CCA380285636LRP4c.1421A>G (p.Asp474Gly)
c.1634A>G (p.Asp545Gly)
c.617A>G (p.Asp206Gly)
11g.46894708T>GCA380285638LRP4c.1421A>C (p.Asp474Ala)
c.1634A>C (p.Asp545Ala)
c.617A>C (p.Asp206Ala)
11g.46894709C>ACA380285647LRP4c.1420G>T (p.Asp474Tyr)
c.1633G>T (p.Asp545Tyr)
c.616G>T (p.Asp206Tyr)
11g.46894709C>GCA380285645LRP4c.1420G>C (p.Asp474His)
c.1633G>C (p.Asp545His)
c.616G>C (p.Asp206His)
11g.46894709C>TCA380285643LRP4c.1420G>A (p.Asp474Asn)
c.1633G>A (p.Asp545Asn)
c.616G>A (p.Asp206Asn)
11g.46894710A>CCA474204981LRP4c.1419T>G (p.Leu473=)
c.1632T>G (p.Leu544=)
c.615T>G (p.Leu205=)
11g.46894710A>GCA474204983LRP4c.1419T>C (p.Leu473=)
c.1632T>C (p.Leu544=)
c.615T>C (p.Leu205=)
11g.46894710A>TCA474204982LRP4c.1419T>A (p.Leu473=)
c.1632T>A (p.Leu544=)
c.615T>A (p.Leu205=)
11g.46894711A>CCA380285650LRP4c.1418T>G (p.Leu473Arg)
c.1631T>G (p.Leu544Arg)
c.614T>G (p.Leu205Arg)
11g.46894711A>GCA380285653LRP4c.1418T>C (p.Leu473Pro)
c.1631T>C (p.Leu544Pro)
c.614T>C (p.Leu205Pro)
11g.46894711A>TCA380285655LRP4c.1418T>A (p.Leu473His)
c.1631T>A (p.Leu544His)
c.614T>A (p.Leu205His)
11g.46894712G>ACA380285658LRP4c.1417C>T (p.Leu473Phe)
c.1630C>T (p.Leu544Phe)
c.613C>T (p.Leu205Phe)
 gnomAD v4
11g.46894712G>CCA380285665LRP4c.1417C>G (p.Leu473Val)
c.1630C>G (p.Leu544Val)
c.613C>G (p.Leu205Val)
11g.46894712G>TCA380285666LRP4c.1417C>A (p.Leu473Ile)
c.1630C>A (p.Leu544Ile)
c.613C>A (p.Leu205Ile)
11g.46894713G>ACA474204984LRP4c.1416C>T (p.Ala472=)
c.1629C>T (p.Ala543=)
c.612C>T (p.Ala204=)
 dbSNP
11g.46894713G>CCA474204985LRP4c.1416C>G (p.Ala472=)
c.1629C>G (p.Ala543=)
c.612C>G (p.Ala204=)
11g.46894713G=CA1969144861LRP4c.1416C= (p.Ala472=)
c.1629C= (p.Ala543=)
c.612C= (p.Ala204=)
11g.46894713G>TCA474204986LRP4c.1416C>A (p.Ala472=)
c.1629C>A (p.Ala543=)
c.612C>A (p.Ala204=)
11g.46894714G>ACA380285668LRP4c.1415C>T (p.Ala472Val)
c.1628C>T (p.Ala543Val)
c.611C>T (p.Ala204Val)
11g.46894714G>CCA380285674LRP4c.1415C>G (p.Ala472Gly)
c.1628C>G (p.Ala543Gly)
c.611C>G (p.Ala204Gly)
11g.46894714G>TCA380285671LRP4c.1415C>A (p.Ala472Asp)
c.1628C>A (p.Ala543Asp)
c.611C>A (p.Ala204Asp)
11g.46894715C>ACA380285685LRP4c.1414G>T (p.Ala472Ser)
c.1627G>T (p.Ala543Ser)
c.610G>T (p.Ala204Ser)
11g.46894715C=CA1969144864LRP4c.1414G= (p.Ala472=)
c.1627G= (p.Ala543=)
c.610G= (p.Ala204=)
11g.46894715C>GCA380285688LRP4c.1414G>C (p.Ala472Pro)
c.1627G>C (p.Ala543Pro)
c.610G>C (p.Ala204Pro)
11g.46894715C>TCA380285690LRP4c.1414G>A (p.Ala472Thr)
c.1627G>A (p.Ala543Thr)
c.610G>A (p.Ala204Thr)
 dbSNP
11g.46894716A=CA1969144867LRP4c.1413T= (p.Ile471=)
c.1626T= (p.Ile542=)
c.609T= (p.Ile203=)
11g.46894716A>CCA380285693LRP4c.1413T>G (p.Ile471Met)
c.1626T>G (p.Ile542Met)
c.609T>G (p.Ile203Met)
 dbSNP gnomAD v4
11g.46894716A>GCA474204987LRP4c.1413T>C (p.Ile471=)
c.1626T>C (p.Ile542=)
c.609T>C (p.Ile203=)
11g.46894716A>TCA474204988LRP4c.1413T>A (p.Ile471=)
c.1626T>A (p.Ile542=)
c.609T>A (p.Ile203=)
11g.46894717A>CCA380285697LRP4c.1412T>G (p.Ile471Ser)
c.1625T>G (p.Ile542Ser)
c.608T>G (p.Ile203Ser)
11g.46894717A>GCA380285707LRP4c.1412T>C (p.Ile471Thr)
c.1625T>C (p.Ile542Thr)
c.608T>C (p.Ile203Thr)
11g.46894717A>TCA380285709LRP4c.1412T>A (p.Ile471Asn)
c.1625T>A (p.Ile542Asn)
c.608T>A (p.Ile203Asn)
11g.46894718T>ACA380285711LRP4c.1411A>T (p.Ile471Phe)
c.1624A>T (p.Ile542Phe)
c.607A>T (p.Ile203Phe)
11g.46894718T>CCA380285713LRP4c.1411A>G (p.Ile471Val)
c.1624A>G (p.Ile542Val)
c.607A>G (p.Ile203Val)
11g.46894718T>GCA380285715LRP4c.1411A>C (p.Ile471Leu)
c.1624A>C (p.Ile542Leu)
c.607A>C (p.Ile203Leu)
11g.46894719G>ACA474204990LRP4c.1410C>T (p.Ala470=)
c.1623C>T (p.Ala541=)
c.606C>T (p.Ala202=)
11g.46894719G>CCA474204991LRP4c.1410C>G (p.Ala470=)
c.1623C>G (p.Ala541=)
c.606C>G (p.Ala202=)
11g.46894719G>TCA474204989LRP4c.1410C>A (p.Ala470=)
c.1623C>A (p.Ala541=)
c.606C>A (p.Ala202=)
11g.46894720G>ACA380285717LRP4c.1409C>T (p.Ala470Val)
c.1622C>T (p.Ala541Val)
c.605C>T (p.Ala202Val)
11g.46894720G>CCA380285720LRP4c.1409C>G (p.Ala470Gly)
c.1622C>G (p.Ala541Gly)
c.605C>G (p.Ala202Gly)
11g.46894720G>TCA380285718LRP4c.1409C>A (p.Ala470Asp)
c.1622C>A (p.Ala541Asp)
c.605C>A (p.Ala202Asp)
11g.46894721C>ACA380285724LRP4c.1408G>T (p.Ala470Ser)
c.1621G>T (p.Ala541Ser)
c.604G>T (p.Ala202Ser)
11g.46894721C>GCA380285725LRP4c.1408G>C (p.Ala470Pro)
c.1621G>C (p.Ala541Pro)
c.604G>C (p.Ala202Pro)
11g.46894721C>TCA380285727LRP4c.1408G>A (p.Ala470Thr)
c.1621G>A (p.Ala541Thr)
c.604G>A (p.Ala202Thr)
11g.46894722A>CCA380285728LRP4c.1407T>G (p.Asn469Lys)
c.1620T>G (p.Asn540Lys)
c.603T>G (p.Asn201Lys)
11g.46894722A>GCA474204992LRP4c.1407T>C (p.Asn469=)
c.1620T>C (p.Asn540=)
c.603T>C (p.Asn201=)
11g.46894722A>TCA380285730LRP4c.1407T>A (p.Asn469Lys)
c.1620T>A (p.Asn540Lys)
c.603T>A (p.Asn201Lys)
11g.46894723T>ACA380285733LRP4c.1406A>T (p.Asn469Ile)
c.1619A>T (p.Asn540Ile)
c.602A>T (p.Asn201Ile)
11g.46894723T>CCA380285734LRP4c.1406A>G (p.Asn469Ser)
c.1619A>G (p.Asn540Ser)
c.602A>G (p.Asn201Ser)
 COSMIC
11g.46894723T>GCA380285737LRP4c.1406A>C (p.Asn469Thr)
c.1619A>C (p.Asn540Thr)
c.602A>C (p.Asn201Thr)
11g.46894724T>ACA380285739LRP4c.1405A>T (p.Asn469Tyr)
c.1618A>T (p.Asn540Tyr)
c.601A>T (p.Asn201Tyr)
11g.46894724T>CCA380285741LRP4c.1405A>G (p.Asn469Asp)
c.1618A>G (p.Asn540Asp)
c.601A>G (p.Asn201Asp)
11g.46894724T>GCA380285743LRP4c.1405A>C (p.Asn469His)
c.1618A>C (p.Asn540His)
c.601A>C (p.Asn201His)
11g.46894725C>ACA380285745LRP4c.1404G>T (p.Glu468Asp)
c.1617G>T (p.Glu539Asp)
c.600G>T (p.Glu200Asp)
11g.46894725C=CA1969144870LRP4c.1404G= (p.Glu468=)
c.1617G= (p.Glu539=)
c.600G= (p.Glu200=)
11g.46894725C>GCA380285746LRP4c.1404G>C (p.Glu468Asp)
c.1617G>C (p.Glu539Asp)
c.600G>C (p.Glu200Asp)
11g.46894725C>TCA5970157LRP4c.1404G>A (p.Glu468=)
c.1617G>A (p.Glu539=)
c.600G>A (p.Glu200=)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894726T>ACA380285753LRP4c.1403A>T (p.Glu468Val)
c.1616A>T (p.Glu539Val)
c.599A>T (p.Glu200Val)
11g.46894726T>CCA380285751LRP4c.1403A>G (p.Glu468Gly)
c.1616A>G (p.Glu539Gly)
c.599A>G (p.Glu200Gly)
11g.46894726T>GCA380285749LRP4c.1403A>C (p.Glu468Ala)
c.1616A>C (p.Glu539Ala)
c.599A>C (p.Glu200Ala)
11g.46894727C>ACA380285755LRP4c.1402G>T (p.Glu468Ter)
c.1615G>T (p.Glu539Ter)
c.598G>T (p.Glu200Ter)
11g.46894727C>GCA380285757LRP4c.1402G>C (p.Glu468Gln)
c.1615G>C (p.Glu539Gln)
c.598G>C (p.Glu200Gln)
11g.46894727C>TCA380285759LRP4c.1402G>A (p.Glu468Lys)
c.1615G>A (p.Glu539Lys)
c.598G>A (p.Glu200Lys)
11g.46894728C>ACA474204993LRP4c.1401G>T (p.Leu467=)
c.1614G>T (p.Leu538=)
c.597G>T (p.Leu199=)
11g.46894728C>GCA474204994LRP4c.1401G>C (p.Leu467=)
c.1614G>C (p.Leu538=)
c.597G>C (p.Leu199=)
11g.46894728C>TCA474204995LRP4c.1401G>A (p.Leu467=)
c.1614G>A (p.Leu538=)
c.597G>A (p.Leu199=)
11g.46894729A>CCA380285761LRP4c.1400T>G (p.Leu467Arg)
c.1613T>G (p.Leu538Arg)
c.596T>G (p.Leu199Arg)
11g.46894729A>GCA380285763LRP4c.1400T>C (p.Leu467Pro)
c.1613T>C (p.Leu538Pro)
c.596T>C (p.Leu199Pro)
11g.46894729A>TCA380285764LRP4c.1400T>A (p.Leu467Gln)
c.1613T>A (p.Leu538Gln)
c.596T>A (p.Leu199Gln)
11g.46894730G>ACA221647446LRP4c.1399C>T (p.Leu467=)
c.1612C>T (p.Leu538=)
c.595C>T (p.Leu199=)
 dbSNP gnomAD v3 gnomAD v4
11g.46894730G>CCA380285767LRP4c.1399C>G (p.Leu467Val)
c.1612C>G (p.Leu538Val)
c.595C>G (p.Leu199Val)
11g.46894730G=CA1969144873LRP4c.1399C= (p.Leu467=)
c.1612C= (p.Leu538=)
c.595C= (p.Leu199=)
11g.46894730G>TCA380285769LRP4c.1399C>A (p.Leu467Met)
c.1612C>A (p.Leu538Met)
c.595C>A (p.Leu199Met)
11g.46894731G>ACA474204996LRP4c.1398C>T (p.Asn466=)
c.1611C>T (p.Asn537=)
c.594C>T (p.Asn198=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894731G>CCA380285771LRP4c.1398C>G (p.Asn466Lys)
c.1611C>G (p.Asn537Lys)
c.594C>G (p.Asn198Lys)
11g.46894731G=CA1969144876LRP4c.1398C= (p.Asn466=)
c.1611C= (p.Asn537=)
c.594C= (p.Asn198=)
11g.46894731G>TCA380285773LRP4c.1398C>A (p.Asn466Lys)
c.1611C>A (p.Asn537Lys)
c.594C>A (p.Asn198Lys)
 gnomAD v4
11g.46894732T>ACA380285775LRP4c.1397A>T (p.Asn466Ile)
c.1610A>T (p.Asn537Ile)
c.593A>T (p.Asn198Ile)
11g.46894732T>CCA380285776LRP4c.1397A>G (p.Asn466Ser)
c.1610A>G (p.Asn537Ser)
c.593A>G (p.Asn198Ser)
 gnomAD v4
11g.46894732T>GCA380285779LRP4c.1397A>C (p.Asn466Thr)
c.1610A>C (p.Asn537Thr)
c.593A>C (p.Asn198Thr)
11g.46894733T>ACA380285783LRP4c.1396A>T (p.Asn466Tyr)
c.1609A>T (p.Asn537Tyr)
c.592A>T (p.Asn198Tyr)
11g.46894733T>CCA380285785LRP4c.1396A>G (p.Asn466Asp)
c.1609A>G (p.Asn537Asp)
c.592A>G (p.Asn198Asp)
11g.46894733T>GCA380285781LRP4c.1396A>C (p.Asn466His)
c.1609A>C (p.Asn537His)
c.592A>C (p.Asn198His)
11g.46894734G>ACA474204997LRP4c.1395C>T (p.Asn465=)
c.1608C>T (p.Asn536=)
c.591C>T (p.Asn197=)
 dbSNP gnomAD v2 gnomAD v4
11g.46894734G>CCA380285787LRP4c.1395C>G (p.Asn465Lys)
c.1608C>G (p.Asn536Lys)
c.591C>G (p.Asn197Lys)
11g.46894734G=CA1969144878LRP4c.1395C= (p.Asn465=)
c.1608C= (p.Asn536=)
c.591C= (p.Asn197=)
11g.46894734G>TCA380285789LRP4c.1395C>A (p.Asn465Lys)
c.1608C>A (p.Asn536Lys)
c.591C>A (p.Asn197Lys)
11g.46894735T>ACA380285792LRP4c.1394A>T (p.Asn465Ile)
c.1607A>T (p.Asn536Ile)
c.590A>T (p.Asn197Ile)
11g.46894735T>CCA380285794LRP4c.1394A>G (p.Asn465Ser)
c.1607A>G (p.Asn536Ser)
c.590A>G (p.Asn197Ser)
 gnomAD v4
11g.46894735T>GCA380285798LRP4c.1394A>C (p.Asn465Thr)
c.1607A>C (p.Asn536Thr)
c.590A>C (p.Asn197Thr)
 gnomAD v4
11g.46894736T>ACA380285804LRP4c.1393A>T (p.Asn465Tyr)
c.1606A>T (p.Asn536Tyr)
c.589A>T (p.Asn197Tyr)
11g.46894736T>CCA380285802LRP4c.1393A>G (p.Asn465Asp)
c.1606A>G (p.Asn536Asp)
c.589A>G (p.Asn197Asp)
11g.46894736T>GCA380285799LRP4c.1393A>C (p.Asn465His)
c.1606A>C (p.Asn536His)
c.589A>C (p.Asn197His)
11g.46894737A>CCA474204998LRP4c.1392T>G (p.Leu464=)
c.1605T>G (p.Leu535=)
c.588T>G (p.Leu196=)
11g.46894737A>GCA474204999LRP4c.1392T>C (p.Leu464=)
c.1605T>C (p.Leu535=)
c.588T>C (p.Leu196=)
11g.46894737A>TCA474205000LRP4c.1392T>A (p.Leu464=)
c.1605T>A (p.Leu535=)
c.588T>A (p.Leu196=)
11g.46894738A>CCA380285806LRP4c.1391T>G (p.Leu464Arg)
c.1604T>G (p.Leu535Arg)
c.587T>G (p.Leu196Arg)
11g.46894738A>GCA380285808LRP4c.1391T>C (p.Leu464Pro)
c.1604T>C (p.Leu535Pro)
c.587T>C (p.Leu196Pro)
11g.46894738A>TCA380285810LRP4c.1391T>A (p.Leu464His)
c.1604T>A (p.Leu535His)
c.587T>A (p.Leu196His)
11g.46894739G>ACA380285812LRP4c.1390C>T (p.Leu464Phe)
c.1603C>T (p.Leu535Phe)
c.586C>T (p.Leu196Phe)
11g.46894739G>CCA380285814LRP4c.1390C>G (p.Leu464Val)
c.1603C>G (p.Leu535Val)
c.586C>G (p.Leu196Val)
11g.46894739G>TCA380285815LRP4c.1390C>A (p.Leu464Ile)
c.1603C>A (p.Leu535Ile)
c.586C>A (p.Leu196Ile)
11g.46894740C>ACA474205002LRP4c.1389G>T (p.Leu463=)
c.1602G>T (p.Leu534=)
c.585G>T (p.Leu195=)
11g.46894740C>GCA474205003LRP4c.1389G>C (p.Leu463=)
c.1602G>C (p.Leu534=)
c.585G>C (p.Leu195=)
11g.46894740C>TCA474205001LRP4c.1389G>A (p.Leu463=)
c.1602G>A (p.Leu534=)
c.585G>A (p.Leu195=)
 gnomAD v4
11g.46894741A>CCA380285818LRP4c.1388T>G (p.Leu463Arg)
c.1601T>G (p.Leu534Arg)
c.584T>G (p.Leu195Arg)
11g.46894741A>GCA380285823LRP4c.1388T>C (p.Leu463Pro)
c.1601T>C (p.Leu534Pro)
c.584T>C (p.Leu195Pro)
11g.46894741A>TCA380285821LRP4c.1388T>A (p.Leu463Gln)
c.1601T>A (p.Leu534Gln)
c.584T>A (p.Leu195Gln)
11g.46894742G>ACA221647447LRP4c.1387C>T (p.Leu463=)
c.1600C>T (p.Leu534=)
c.583C>T (p.Leu195=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894742G>CCA380285824LRP4c.1387C>G (p.Leu463Val)
c.1600C>G (p.Leu534Val)
c.583C>G (p.Leu195Val)
11g.46894742G=CA1969144882LRP4c.1387C= (p.Leu463=)
c.1600C= (p.Leu534=)
c.583C= (p.Leu195=)
11g.46894742G>TCA380285825LRP4c.1387C>A (p.Leu463Met)
c.1600C>A (p.Leu534Met)
c.583C>A (p.Leu195Met)
11g.46894743C>ACA474205004LRP4c.1386G>T (p.Leu462=)
c.1599G>T (p.Leu533=)
c.582G>T (p.Leu194=)
11g.46894743C>GCA474205005LRP4c.1386G>C (p.Leu462=)
c.1599G>C (p.Leu533=)
c.582G>C (p.Leu194=)
11g.46894743C>TCA474205006LRP4c.1386G>A (p.Leu462=)
c.1599G>A (p.Leu533=)
c.582G>A (p.Leu194=)
11g.46894744A>CCA380285827LRP4c.1385T>G (p.Leu462Arg)
c.1598T>G (p.Leu533Arg)
c.581T>G (p.Leu194Arg)
11g.46894744A>GCA380285828LRP4c.1385T>C (p.Leu462Pro)
c.1598T>C (p.Leu533Pro)
c.581T>C (p.Leu194Pro)
11g.46894744A>TCA380285831LRP4c.1385T>A (p.Leu462Gln)
c.1598T>A (p.Leu533Gln)
c.581T>A (p.Leu194Gln)
11g.46894745G>ACA474205007LRP4c.1384C>T (p.Leu462=)
c.1597C>T (p.Leu533=)
c.580C>T (p.Leu194=)
 gnomAD v4
11g.46894745G>CCA380285833LRP4c.1384C>G (p.Leu462Val)
c.1597C>G (p.Leu533Val)
c.580C>G (p.Leu194Val)
 gnomAD v4
11g.46894745G>TCA380285835LRP4c.1384C>A (p.Leu462Met)
c.1597C>A (p.Leu533Met)
c.580C>A (p.Leu194Met)
11g.46894746T>ACA474205008LRP4c.1383A>T (p.Thr461=)
c.1596A>T (p.Thr532=)
c.579A>T (p.Thr193=)
11g.46894746T>CCA5970158LRP4c.1383A>G (p.Thr461=)
c.1596A>G (p.Thr532=)
c.579A>G (p.Thr193=)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894746T>GCA474205009LRP4c.1383A>C (p.Thr461=)
c.1596A>C (p.Thr532=)
c.579A>C (p.Thr193=)
11g.46894746T=CA1969144884LRP4c.1383A= (p.Thr461=)
c.1596A= (p.Thr532=)
c.579A= (p.Thr193=)
11g.46894747G>ACA380285839LRP4c.1382C>T (p.Thr461Ile)
c.1595C>T (p.Thr532Ile)
c.578C>T (p.Thr193Ile)
11g.46894747G>CCA5970159LRP4c.1382C>G (p.Thr461Arg)
c.1595C>G (p.Thr532Arg)
c.578C>G (p.Thr193Arg)
 dbSNP ExAC gnomAD v4
11g.46894747G=CA1969144889LRP4c.1382C= (p.Thr461=)
c.1595C= (p.Thr532=)
c.578C= (p.Thr193=)
11g.46894747G>TCA380285841LRP4c.1382C>A (p.Thr461Lys)
c.1595C>A (p.Thr532Lys)
c.578C>A (p.Thr193Lys)
11g.46894748T>ACA380285843LRP4c.1381A>T (p.Thr461Ser)
c.1594A>T (p.Thr532Ser)
c.577A>T (p.Thr193Ser)
 gnomAD v4
11g.46894748T>CCA380285845LRP4c.1381A>G (p.Thr461Ala)
c.1594A>G (p.Thr532Ala)
c.577A>G (p.Thr193Ala)
 dbSNP gnomAD v2 gnomAD v4
11g.46894748T>GCA117688LRP4c.1381A>C (p.Thr461Pro)
c.1594A>C (p.Thr532Pro)
c.577A>C (p.Thr193Pro)
 ClinVar dbSNP
11g.46894748T=CA1969144893LRP4c.1381A= (p.Thr461=)
c.1594A= (p.Thr532=)
c.577A= (p.Thr193=)
11g.46894749G>ACA5970160LRP4c.1380C>T (p.Tyr460=)
c.1593C>T (p.Tyr531=)
c.576C>T (p.Tyr192=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894749G>CCA380285848LRP4c.1380C>G (p.Tyr460Ter)
c.1593C>G (p.Tyr531Ter)
c.576C>G (p.Tyr192Ter)
11g.46894749G=CA1969144899LRP4c.1380C= (p.Tyr460=)
c.1593C= (p.Tyr531=)
c.576C= (p.Tyr192=)
11g.46894749G>TCA380285850LRP4c.1380C>A (p.Tyr460Ter)
c.1593C>A (p.Tyr531Ter)
c.576C>A (p.Tyr192Ter)
11g.46894750T>ACA380285852LRP4c.1379A>T (p.Tyr460Phe)
c.1592A>T (p.Tyr531Phe)
c.575A>T (p.Tyr192Phe)
11g.46894750T>CCA380285854LRP4c.1379A>G (p.Tyr460Cys)
c.1592A>G (p.Tyr531Cys)
c.575A>G (p.Tyr192Cys)
 gnomAD v4
11g.46894750T>GCA380285856LRP4c.1379A>C (p.Tyr460Ser)
c.1592A>C (p.Tyr531Ser)
c.575A>C (p.Tyr192Ser)
11g.46894751A>CCA380285862LRP4c.1378T>G (p.Tyr460Asp)
c.1591T>G (p.Tyr531Asp)
c.574T>G (p.Tyr192Asp)
11g.46894751A>GCA380285858LRP4c.1378T>C (p.Tyr460His)
c.1591T>C (p.Tyr531His)
c.574T>C (p.Tyr192His)
11g.46894751A>TCA380285860LRP4c.1378T>A (p.Tyr460Asn)
c.1591T>A (p.Tyr531Asn)
c.574T>A (p.Tyr192Asn)
11g.46894752C>ACA380285863LRP4c.1377G>T (p.Glu459Asp)
c.1590G>T (p.Glu530Asp)
c.573G>T (p.Glu191Asp)
11g.46894752C>GCA380285864LRP4c.1377G>C (p.Glu459Asp)
c.1590G>C (p.Glu530Asp)
c.573G>C (p.Glu191Asp)
11g.46894752C>TCA474205010LRP4c.1377G>A (p.Glu459=)
c.1590G>A (p.Glu530=)
c.573G>A (p.Glu191=)
11g.46894753T>ACA380285865LRP4c.1376A>T (p.Glu459Val)
c.1589A>T (p.Glu530Val)
c.572A>T (p.Glu191Val)
11g.46894753T>CCA380285867LRP4c.1376A>G (p.Glu459Gly)
c.1589A>G (p.Glu530Gly)
c.572A>G (p.Glu191Gly)
11g.46894753T>GCA380285872LRP4c.1376A>C (p.Glu459Ala)
c.1589A>C (p.Glu530Ala)
c.572A>C (p.Glu191Ala)
11g.46894754C>ACA380285875LRP4c.1375G>T (p.Glu459Ter)
c.1588G>T (p.Glu530Ter)
c.571G>T (p.Glu191Ter)
11g.46894754C>GCA380285873LRP4c.1375G>C (p.Glu459Gln)
c.1588G>C (p.Glu530Gln)
c.571G>C (p.Glu191Gln)
11g.46894754C>TCA380285874LRP4c.1375G>A (p.Glu459Lys)
c.1588G>A (p.Glu530Lys)
c.571G>A (p.Glu191Lys)
11g.46894755A>CCA474205011LRP4c.1374T>G (p.Ser458=)
c.1587T>G (p.Ser529=)
c.570T>G (p.Ser190=)
11g.46894755A>GCA474205012LRP4c.1374T>C (p.Ser458=)
c.1587T>C (p.Ser529=)
c.570T>C (p.Ser190=)
11g.46894755A>TCA474205013LRP4c.1374T>A (p.Ser458=)
c.1587T>A (p.Ser529=)
c.570T>A (p.Ser190=)
11g.46894757_46894758delCA2613350020LRP4c.1373_1374del (p.Ser458Ter)
c.1586_1587del (p.Ser529Ter)
c.569_570del (p.Ser190Ter)
 gnomAD v4
11g.46894756G>ACA380285876LRP4c.1373C>T (p.Ser458Phe)
c.1586C>T (p.Ser529Phe)
c.569C>T (p.Ser190Phe)
11g.46894756G>CCA380285877LRP4c.1373C>G (p.Ser458Cys)
c.1586C>G (p.Ser529Cys)
c.569C>G (p.Ser190Cys)
11g.46894756G>TCA380285878LRP4c.1373C>A (p.Ser458Tyr)
c.1586C>A (p.Ser529Tyr)
c.569C>A (p.Ser190Tyr)
11g.46894757A>CCA380285879LRP4c.1372T>G (p.Ser458Ala)
c.1585T>G (p.Ser529Ala)
c.568T>G (p.Ser190Ala)
11g.46894757A>GCA380285880LRP4c.1372T>C (p.Ser458Pro)
c.1585T>C (p.Ser529Pro)
c.568T>C (p.Ser190Pro)
11g.46894757A>TCA380285881LRP4c.1372T>A (p.Ser458Thr)
c.1585T>A (p.Ser529Thr)
c.568T>A (p.Ser190Thr)
11g.46894758G>ACA474205014LRP4c.1371C>T (p.Arg457=)
c.1584C>T (p.Arg528=)
c.567C>T (p.Arg189=)
11g.46894758G>CCA474205015LRP4c.1371C>G (p.Arg457=)
c.1584C>G (p.Arg528=)
c.567C>G (p.Arg189=)
11g.46894758G=CA1969144906LRP4c.1371C= (p.Arg457=)
c.1584C= (p.Arg528=)
c.567C= (p.Arg189=)
11g.46894758G>TCA221647479LRP4c.1371C>A (p.Arg457=)
c.1584C>A (p.Arg528=)
c.567C>A (p.Arg189=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894759C>ACA380285882LRP4c.1370G>T (p.Arg457Leu)
c.1583G>T (p.Arg528Leu)
c.566G>T (p.Arg189Leu)
11g.46894759C=CA1969144912LRP4c.1370G= (p.Arg457=)
c.1583G= (p.Arg528=)
c.566G= (p.Arg189=)
11g.46894759C>GCA380285883LRP4c.1370G>C (p.Arg457Pro)
c.1583G>C (p.Arg528Pro)
c.566G>C (p.Arg189Pro)
11g.46894759C>TCA5970161LRP4c.1370G>A (p.Arg457His)
c.1583G>A (p.Arg528His)
c.566G>A (p.Arg189His)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894760G>ACA5970162LRP4c.1369C>T (p.Arg457Cys)
c.1582C>T (p.Arg528Cys)
c.565C>T (p.Arg189Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894760G>CCA380285884LRP4c.1369C>G (p.Arg457Gly)
c.1582C>G (p.Arg528Gly)
c.565C>G (p.Arg189Gly)
 dbSNP gnomAD v2 gnomAD v4
11g.46894760G=CA1969144917LRP4c.1369C= (p.Arg457=)
c.1582C= (p.Arg528=)
c.565C= (p.Arg189=)
11g.46894760G>TCA380285885LRP4c.1369C>A (p.Arg457Ser)
c.1582C>A (p.Arg528Ser)
c.565C>A (p.Arg189Ser)
 gnomAD v4
11g.46894761G>ACA5970163LRP4c.1368C>T (p.His456=)
c.1581C>T (p.His527=)
c.564C>T (p.His188=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894761G>CCA380285887LRP4c.1368C>G (p.His456Gln)
c.1581C>G (p.His527Gln)
c.564C>G (p.His188Gln)
11g.46894761G=CA1969144928LRP4c.1368C= (p.His456=)
c.1581C= (p.His527=)
c.564C= (p.His188=)
11g.46894761G>TCA380285886LRP4c.1368C>A (p.His456Gln)
c.1581C>A (p.His527Gln)
c.564C>A (p.His188Gln)
 dbSNP gnomAD v3 gnomAD v4
11g.46894762T>ACA380285888LRP4c.1367A>T (p.His456Leu)
c.1580A>T (p.His527Leu)
c.563A>T (p.His188Leu)
11g.46894762T>CCA380285889LRP4c.1367A>G (p.His456Arg)
c.1580A>G (p.His527Arg)
c.563A>G (p.His188Arg)
11g.46894762T>GCA380285890LRP4c.1367A>C (p.His456Pro)
c.1580A>C (p.His527Pro)
c.563A>C (p.His188Pro)
11g.46894763G>ACA380285891LRP4c.1366C>T (p.His456Tyr)
c.1579C>T (p.His527Tyr)
c.562C>T (p.His188Tyr)
 ClinVar dbSNP gnomAD v4
11g.46894763G>CCA380285892LRP4c.1366C>G (p.His456Asp)
c.1579C>G (p.His527Asp)
c.562C>G (p.His188Asp)
11g.46894763G=CA1969144935LRP4c.1366C= (p.His456=)
c.1579C= (p.His527=)
c.562C= (p.His188=)
11g.46894763G>TCA380285893LRP4c.1366C>A (p.His456Asn)
c.1579C>A (p.His527Asn)
c.562C>A (p.His188Asn)
11g.46894764T>ACA474205016LRP4c.1365A>T (p.Pro455=)
c.1578A>T (p.Pro526=)
c.561A>T (p.Pro187=)
11g.46894764T>CCA5970164LRP4c.1365A>G (p.Pro455=)
c.1578A>G (p.Pro526=)
c.561A>G (p.Pro187=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.46894764T>GCA474205017LRP4c.1365A>C (p.Pro455=)
c.1578A>C (p.Pro526=)
c.561A>C (p.Pro187=)
 gnomAD v4
11g.46894764T=CA1969144944LRP4c.1365A= (p.Pro455=)
c.1578A= (p.Pro526=)
c.561A= (p.Pro187=)
11g.46894764_46894768delCA2574812596LRP4c.1361_1365del (p.Leu454ProfsTer4)
c.1574_1578del (p.Leu525ProfsTer4)
c.557_561del (p.Leu186ProfsTer4)
11g.46894765G>ACA380285894LRP4c.1364C>T (p.Pro455Leu)
c.1577C>T (p.Pro526Leu)
c.560C>T (p.Pro187Leu)
 dbSNP gnomAD v2
11g.46894765G>CCA380285895LRP4c.1364C>G (p.Pro455Arg)
c.1577C>G (p.Pro526Arg)
c.560C>G (p.Pro187Arg)
11g.46894765G=CA1969144949LRP4c.1364C= (p.Pro455=)
c.1577C= (p.Pro526=)
c.560C= (p.Pro187=)
11g.46894765G>TCA380285896LRP4c.1364C>A (p.Pro455Gln)
c.1577C>A (p.Pro526Gln)
c.560C>A (p.Pro187Gln)
11g.46894766G>ACA380285897LRP4c.1363C>T (p.Pro455Ser)
c.1576C>T (p.Pro526Ser)
c.559C>T (p.Pro187Ser)
 dbSNP
11g.46894766G>CCA380285898LRP4c.1363C>G (p.Pro455Ala)
c.1576C>G (p.Pro526Ala)
c.559C>G (p.Pro187Ala)
11g.46894766G=CA1969144953LRP4c.1363C= (p.Pro455=)
c.1576C= (p.Pro526=)
c.559C= (p.Pro187=)
11g.46894766G>TCA380285899LRP4c.1363C>A (p.Pro455Thr)
c.1576C>A (p.Pro526Thr)
c.559C>A (p.Pro187Thr)
11g.46894767C>ACA474205018LRP4c.1362G>T (p.Leu454=)
c.1575G>T (p.Leu525=)
c.558G>T (p.Leu186=)
11g.46894767C>GCA474205019LRP4c.1362G>C (p.Leu454=)
c.1575G>C (p.Leu525=)
c.558G>C (p.Leu186=)
11g.46894767C>TCA474205020LRP4c.1362G>A (p.Leu454=)
c.1575G>A (p.Leu525=)
c.558G>A (p.Leu186=)
 gnomAD v4
11g.46894768A>CCA380285900LRP4c.1361T>G (p.Leu454Arg)
c.1574T>G (p.Leu525Arg)
c.557T>G (p.Leu186Arg)
11g.46894768A>GCA380285902LRP4c.1361T>C (p.Leu454Pro)
c.1574T>C (p.Leu525Pro)
c.557T>C (p.Leu186Pro)
11g.46894768A>TCA380285901LRP4c.1361T>A (p.Leu454Gln)
c.1574T>A (p.Leu525Gln)
c.557T>A (p.Leu186Gln)
11g.46894769G>ACA474205021LRP4c.1360C>T (p.Leu454=)
c.1573C>T (p.Leu525=)
c.556C>T (p.Leu186=)
 COSMIC
11g.46894769G>CCA380285903LRP4c.1360C>G (p.Leu454Val)
c.1573C>G (p.Leu525Val)
c.556C>G (p.Leu186Val)
11g.46894769G>TCA380285904LRP4c.1360C>A (p.Leu454Met)
c.1573C>A (p.Leu525Met)
c.556C>A (p.Leu186Met)
11g.46894770C>ACA474205022LRP4c.1359G>T (p.Val453=)
c.1572G>T (p.Val524=)
c.555G>T (p.Val185=)
 gnomAD v4
11g.46894770C>GCA474205023LRP4c.1359G>C (p.Val453=)
c.1572G>C (p.Val524=)
c.555G>C (p.Val185=)
11g.46894770C>TCA474205024LRP4c.1359G>A (p.Val453=)
c.1572G>A (p.Val524=)
c.555G>A (p.Val185=)
 gnomAD v4
11g.46894771A=CA1969144957LRP4c.1358T= (p.Val453=)
c.1571T= (p.Val524=)
c.554T= (p.Val185=)
11g.46894771A>CCA380285905LRP4c.1358T>G (p.Val453Gly)
c.1571T>G (p.Val524Gly)
c.554T>G (p.Val185Gly)
 dbSNP gnomAD v4
11g.46894771A>GCA380285906LRP4c.1358T>C (p.Val453Ala)
c.1571T>C (p.Val524Ala)
c.554T>C (p.Val185Ala)
 gnomAD v4
11g.46894771A>TCA380285907LRP4c.1358T>A (p.Val453Glu)
c.1571T>A (p.Val524Glu)
c.554T>A (p.Val185Glu)
11g.46894772C>ACA380285908LRP4c.1357G>T (p.Val453Leu)
c.1570G>T (p.Val524Leu)
c.553G>T (p.Val185Leu)
 gnomAD v4
11g.46894772C>GCA380285909LRP4c.1357G>C (p.Val453Leu)
c.1570G>C (p.Val524Leu)
c.553G>C (p.Val185Leu)
11g.46894772C>TCA380285910LRP4c.1357G>A (p.Val453Met)
c.1570G>A (p.Val524Met)
c.553G>A (p.Val185Met)
11g.46894773C>ACA380285911LRP4c.1356G>T (p.Gln452His)
c.1569G>T (p.Gln523His)
c.552G>T (p.Gln184His)
11g.46894773C>GCA380285912LRP4c.1356G>C (p.Gln452His)
c.1569G>C (p.Gln523His)
c.552G>C (p.Gln184His)
11g.46894773C>TCA474205025LRP4c.1356G>A (p.Gln452=)
c.1569G>A (p.Gln523=)
c.552G>A (p.Gln184=)
11g.46894774T>ACA380285913LRP4c.1355A>T (p.Gln452Leu)
c.1568A>T (p.Gln523Leu)
c.551A>T (p.Gln184Leu)
11g.46894774T>CCA380285915LRP4c.1355A>G (p.Gln452Arg)
c.1568A>G (p.Gln523Arg)
c.551A>G (p.Gln184Arg)
11g.46894774T>GCA380285914LRP4c.1355A>C (p.Gln452Pro)
c.1568A>C (p.Gln523Pro)
c.551A>C (p.Gln184Pro)
11g.46894775G>ACA380285916LRP4c.1354C>T (p.Gln452Ter)
c.1567C>T (p.Gln523Ter)
c.550C>T (p.Gln184Ter)
11g.46894775G>CCA380285918LRP4c.1354C>G (p.Gln452Glu)
c.1567C>G (p.Gln523Glu)
c.550C>G (p.Gln184Glu)
11g.46894775G>TCA380285917LRP4c.1354C>A (p.Gln452Lys)
c.1567C>A (p.Gln523Lys)
c.550C>A (p.Gln184Lys)
11g.46894776C>ACA474205028LRP4c.1353G>T (p.Arg451=)
c.1566G>T (p.Arg522=)
c.549G>T (p.Arg183=)
11g.46894776C=CA1969144961LRP4c.1353G= (p.Arg451=)
c.1566G= (p.Arg522=)
c.549G= (p.Arg183=)
11g.46894776C>GCA474205027LRP4c.1353G>C (p.Arg451=)
c.1566G>C (p.Arg522=)
c.549G>C (p.Arg183=)
 dbSNP gnomAD v2 gnomAD v4
11g.46894776C>TCA474205026LRP4c.1353G>A (p.Arg451=)
c.1566G>A (p.Arg522=)
c.549G>A (p.Arg183=)
11g.46894777C>ACA380285919LRP4c.1352G>T (p.Arg451Leu)
c.1565G>T (p.Arg522Leu)
c.548G>T (p.Arg183Leu)
11g.46894777C=CA1969144964LRP4c.1352G= (p.Arg451=)
c.1565G= (p.Arg522=)
c.548G= (p.Arg183=)
11g.46894777C>GCA380285920LRP4c.1352G>C (p.Arg451Pro)
c.1565G>C (p.Arg522Pro)
c.548G>C (p.Arg183Pro)
11g.46894777C>TCA221647504LRP4c.1352G>A (p.Arg451Gln)
c.1565G>A (p.Arg522Gln)
c.548G>A (p.Arg183Gln)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894778G>ACA5970165LRP4c.1351C>T (p.Arg451Trp)
c.1564C>T (p.Arg522Trp)
c.547C>T (p.Arg183Trp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
11g.46894778G>CCA380285921LRP4c.1351C>G (p.Arg451Gly)
c.1564C>G (p.Arg522Gly)
c.547C>G (p.Arg183Gly)
 dbSNP gnomAD v2
11g.46894778G=CA1969144970LRP4c.1351C= (p.Arg451=)
c.1564C= (p.Arg522=)
c.547C= (p.Arg183=)
11g.46894778G>TCA474205029LRP4c.1351C>A (p.Arg451=)
c.1564C>A (p.Arg522=)
c.547C>A (p.Arg183=)
11g.46894779G>ACA5970166LRP4c.1350C>T (p.Ile450=)
c.1563C>T (p.Ile521=)
c.546C>T (p.Ile182=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894779G>CCA380285922LRP4c.1350C>G (p.Ile450Met)
c.1563C>G (p.Ile521Met)
c.546C>G (p.Ile182Met)
11g.46894779G=CA1969144978LRP4c.1350C= (p.Ile450=)
c.1563C= (p.Ile521=)
c.546C= (p.Ile182=)
11g.46894779G>TCA474205030LRP4c.1350C>A (p.Ile450=)
c.1563C>A (p.Ile521=)
c.546C>A (p.Ile182=)
11g.46894780A>CCA380285923LRP4c.1349T>G (p.Ile450Ser)
c.1562T>G (p.Ile521Ser)
c.545T>G (p.Ile182Ser)
11g.46894780A>GCA380285924LRP4c.1349T>C (p.Ile450Thr)
c.1562T>C (p.Ile521Thr)
c.545T>C (p.Ile182Thr)
11g.46894780A>TCA380285925LRP4c.1349T>A (p.Ile450Asn)
c.1562T>A (p.Ile521Asn)
c.545T>A (p.Ile182Asn)
11g.46894781T>ACA380285926LRP4c.1348A>T (p.Ile450Phe)
c.1561A>T (p.Ile521Phe)
c.544A>T (p.Ile182Phe)
11g.46894781T>CCA380285927LRP4c.1348A>G (p.Ile450Val)
c.1561A>G (p.Ile521Val)
c.544A>G (p.Ile182Val)
11g.46894781T>GCA380285928LRP4c.1348A>C (p.Ile450Leu)
c.1561A>C (p.Ile521Leu)
c.544A>C (p.Ile182Leu)
11g.46894782G>ACA5970167LRP4c.1347C>T (p.Asp449=)
c.1560C>T (p.Asp520=)
c.543C>T (p.Asp181=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894782G>CCA380285929LRP4c.1347C>G (p.Asp449Glu)
c.1560C>G (p.Asp520Glu)
c.543C>G (p.Asp181Glu)
11g.46894782G=CA1969144981LRP4c.1347C= (p.Asp449=)
c.1560C= (p.Asp520=)
c.543C= (p.Asp181=)
11g.46894782G>TCA380285930LRP4c.1347C>A (p.Asp449Glu)
c.1560C>A (p.Asp520Glu)
c.543C>A (p.Asp181Glu)
11g.46894783T>ACA380285933LRP4c.1346A>T (p.Asp449Val)
c.1559A>T (p.Asp520Val)
c.542A>T (p.Asp181Val)
11g.46894783T>CCA380285932LRP4c.1346A>G (p.Asp449Gly)
c.1559A>G (p.Asp520Gly)
c.542A>G (p.Asp181Gly)
11g.46894783T>GCA380285931LRP4c.1346A>C (p.Asp449Ala)
c.1559A>C (p.Asp520Ala)
c.542A>C (p.Asp181Ala)
11g.46894784C>ACA380285934LRP4c.1345G>T (p.Asp449Tyr)
c.1558G>T (p.Asp520Tyr)
c.541G>T (p.Asp181Tyr)
11g.46894784C=CA1969144989LRP4c.1345G= (p.Asp449=)
c.1558G= (p.Asp520=)
c.541G= (p.Asp181=)
11g.46894784C>GCA380285935LRP4c.1345G>C (p.Asp449His)
c.1558G>C (p.Asp520His)
c.541G>C (p.Asp181His)
11g.46894784C>TCA117687LRP4c.1345G>A (p.Asp449Asn)
c.1558G>A (p.Asp520Asn)
c.541G>A (p.Asp181Asn)
 ClinVar dbSNP gnomAD v4
11g.46894785G>ACA5970169LRP4c.1344C>T (p.Ile448=)
c.1557C>T (p.Ile519=)
c.540C>T (p.Ile180=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894785G>CCA380285936LRP4c.1344C>G (p.Ile448Met)
c.1557C>G (p.Ile519Met)
c.540C>G (p.Ile180Met)
11g.46894785G=CA1969144998LRP4c.1344C= (p.Ile448=)
c.1557C= (p.Ile519=)
c.540C= (p.Ile180=)
11g.46894785G>TCA5970168LRP4c.1344C>A (p.Ile448=)
c.1557C>A (p.Ile519=)
c.540C>A (p.Ile180=)
 dbSNP ExAC gnomAD v2
11g.46894786A>CCA380285937LRP4c.1343T>G (p.Ile448Ser)
c.1556T>G (p.Ile519Ser)
c.539T>G (p.Ile180Ser)
11g.46894786A>GCA380285938LRP4c.1343T>C (p.Ile448Thr)
c.1556T>C (p.Ile519Thr)
c.539T>C (p.Ile180Thr)
11g.46894786A>TCA380285939LRP4c.1343T>A (p.Ile448Asn)
c.1556T>A (p.Ile519Asn)
c.539T>A (p.Ile180Asn)
11g.46894787T>ACA380285940LRP4c.1342A>T (p.Ile448Phe)
c.1555A>T (p.Ile519Phe)
c.538A>T (p.Ile180Phe)
11g.46894787T>CCA5970170LRP4c.1342A>G (p.Ile448Val)
c.1555A>G (p.Ile519Val)
c.538A>G (p.Ile180Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894787T>GCA380285941LRP4c.1342A>C (p.Ile448Leu)
c.1555A>C (p.Ile519Leu)
c.538A>C (p.Ile180Leu)
11g.46894787T=CA1969145006LRP4c.1342A= (p.Ile448=)
c.1555A= (p.Ile519=)
c.538A= (p.Ile180=)
11g.46894788G>ACA474205031LRP4c.1341C>T (p.Arg447=)
c.1554C>T (p.Arg518=)
c.537C>T (p.Arg179=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894788G>CCA474205032LRP4c.1341C>G (p.Arg447=)
c.1554C>G (p.Arg518=)
c.537C>G (p.Arg179=)
11g.46894788G=CA1969145008LRP4c.1341C= (p.Arg447=)
c.1554C= (p.Arg518=)
c.537C= (p.Arg179=)
11g.46894788G>TCA474205033LRP4c.1341C>A (p.Arg447=)
c.1554C>A (p.Arg518=)
c.537C>A (p.Arg179=)
11g.46894789C>ACA380285944LRP4c.1340G>T (p.Arg447Leu)
c.1553G>T (p.Arg518Leu)
c.536G>T (p.Arg179Leu)
 gnomAD v4
11g.46894789C=CA1969145013LRP4c.1340G= (p.Arg447=)
c.1553G= (p.Arg518=)
c.536G= (p.Arg179=)
11g.46894789C>GCA380285943LRP4c.1340G>C (p.Arg447Pro)
c.1553G>C (p.Arg518Pro)
c.536G>C (p.Arg179Pro)
 dbSNP gnomAD v2
11g.46894789C>TCA380285942LRP4c.1340G>A (p.Arg447His)
c.1553G>A (p.Arg518His)
c.536G>A (p.Arg179His)
 dbSNP gnomAD v4
11g.46894790G>ACA380285945LRP4c.1339C>T (p.Arg447Cys)
c.1552C>T (p.Arg518Cys)
c.535C>T (p.Arg179Cys)
 dbSNP gnomAD v3 gnomAD v4
11g.46894790G>CCA380285946LRP4c.1339C>G (p.Arg447Gly)
c.1552C>G (p.Arg518Gly)
c.535C>G (p.Arg179Gly)
11g.46894790G=CA1969145016LRP4c.1339C= (p.Arg447=)
c.1552C= (p.Arg518=)
c.535C= (p.Arg179=)
11g.46894790G>TCA380285947LRP4c.1339C>A (p.Arg447Ser)
c.1552C>A (p.Arg518Ser)
c.535C>A (p.Arg179Ser)
11g.46894791A>CCA380285948LRP4c.1338T>G (p.Asn446Lys)
c.1551T>G (p.Asn517Lys)
c.534T>G (p.Asn178Lys)
11g.46894791A>GCA474205034LRP4c.1338T>C (p.Asn446=)
c.1551T>C (p.Asn517=)
c.534T>C (p.Asn178=)
11g.46894791A>TCA380285949LRP4c.1338T>A (p.Asn446Lys)
c.1551T>A (p.Asn517Lys)
c.534T>A (p.Asn178Lys)
11g.46894792T>ACA380285950LRP4c.1337A>T (p.Asn446Ile)
c.1550A>T (p.Asn517Ile)
c.533A>T (p.Asn178Ile)
11g.46894792T>CCA221647557LRP4c.1337A>G (p.Asn446Ser)
c.1550A>G (p.Asn517Ser)
c.533A>G (p.Asn178Ser)
 dbSNP gnomAD v4
11g.46894792T>GCA380285951LRP4c.1337A>C (p.Asn446Thr)
c.1550A>C (p.Asn517Thr)
c.533A>C (p.Asn178Thr)
11g.46894792T=CA1969145021LRP4c.1337A= (p.Asn446=)
c.1550A= (p.Asn517=)
c.533A= (p.Asn178=)
11g.46894793T>ACA380285952LRP4c.1336A>T (p.Asn446Tyr)
c.1549A>T (p.Asn517Tyr)
c.532A>T (p.Asn178Tyr)
11g.46894793T>CCA380285953LRP4c.1336A>G (p.Asn446Asp)
c.1549A>G (p.Asn517Asp)
c.532A>G (p.Asn178Asp)
 COSMIC
11g.46894793T>GCA380285954LRP4c.1336A>C (p.Asn446His)
c.1549A>C (p.Asn517His)
c.532A>C (p.Asn178His)
11g.46894794G>ACA474205035LRP4c.1335C>T (p.Ala445=)
c.1548C>T (p.Ala516=)
c.531C>T (p.Ala177=)
 gnomAD v4
11g.46894794G>CCA474205037LRP4c.1335C>G (p.Ala445=)
c.1548C>G (p.Ala516=)
c.531C>G (p.Ala177=)
11g.46894794G>TCA474205036LRP4c.1335C>A (p.Ala445=)
c.1548C>A (p.Ala516=)
c.531C>A (p.Ala177=)

Number of alleles fetched