Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.46894594C>ACA380284936LRP4c.1535G>T (p.Ser512Ile)
c.1748G>T (p.Ser583Ile)
c.731G>T (p.Ser244Ile)
 ClinVar dbSNP gnomAD v4
11g.46894594C=CA1969144645LRP4c.1535G= (p.Ser512=)
c.1748G= (p.Ser583=)
c.731G= (p.Ser244=)
11g.46894594C>GCA380284938LRP4c.1535G>C (p.Ser512Thr)
c.1748G>C (p.Ser583Thr)
c.731G>C (p.Ser244Thr)
11g.46894594C>TCA5970125LRP4c.1535G>A (p.Ser512Asn)
c.1748G>A (p.Ser583Asn)
c.731G>A (p.Ser244Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894595T>ACA5970126LRP4c.1534A>T (p.Ser512Cys)
c.1747A>T (p.Ser583Cys)
c.730A>T (p.Ser244Cys)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894595T>CCA380284943LRP4c.1534A>G (p.Ser512Gly)
c.1747A>G (p.Ser583Gly)
c.730A>G (p.Ser244Gly)
11g.46894595T>GCA380284941LRP4c.1534A>C (p.Ser512Arg)
c.1747A>C (p.Ser583Arg)
c.730A>C (p.Ser244Arg)
11g.46894595T=CA1969144646LRP4c.1534A= (p.Ser512=)
c.1747A= (p.Ser583=)
c.730A= (p.Ser244=)
11g.46894596C>ACA380284946LRP4c.1533G>T (p.Glu511Asp)
c.1746G>T (p.Glu582Asp)
c.729G>T (p.Glu243Asp)
11g.46894596C>GCA380284948LRP4c.1533G>C (p.Glu511Asp)
c.1746G>C (p.Glu582Asp)
c.729G>C (p.Glu243Asp)
 COSMIC
11g.46894596C>TCA474204862LRP4c.1533G>A (p.Glu511=)
c.1746G>A (p.Glu582=)
c.729G>A (p.Glu243=)
11g.46894597T>ACA380284950LRP4c.1532A>T (p.Glu511Val)
c.1745A>T (p.Glu582Val)
c.728A>T (p.Glu243Val)
11g.46894597T>CCA380284952LRP4c.1532A>G (p.Glu511Gly)
c.1745A>G (p.Glu582Gly)
c.728A>G (p.Glu243Gly)
 gnomAD v4
11g.46894597T>GCA5970127LRP4c.1532A>C (p.Glu511Ala)
c.1745A>C (p.Glu582Ala)
c.728A>C (p.Glu243Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894597T=CA1969144647LRP4c.1532A= (p.Glu511=)
c.1745A= (p.Glu582=)
c.728A= (p.Glu243=)
11g.46894598C>ACA380284955LRP4c.1531G>T (p.Glu511Ter)
c.1744G>T (p.Glu582Ter)
c.727G>T (p.Glu243Ter)
11g.46894598C=CA1969144648LRP4c.1531G= (p.Glu511=)
c.1744G= (p.Glu582=)
c.727G= (p.Glu243=)
11g.46894598C>GCA5970128LRP4c.1531G>C (p.Glu511Gln)
c.1744G>C (p.Glu582Gln)
c.727G>C (p.Glu243Gln)
 dbSNP ExAC gnomAD v2
11g.46894598C>TCA380284958LRP4c.1531G>A (p.Glu511Lys)
c.1744G>A (p.Glu582Lys)
c.727G>A (p.Glu243Lys)
11g.46894599C>ACA474204863LRP4c.1530G>T (p.Leu510=)
c.1743G>T (p.Leu581=)
c.726G>T (p.Leu242=)
 dbSNP
11g.46894599C=CA1969144651LRP4c.1530G= (p.Leu510=)
c.1743G= (p.Leu581=)
c.726G= (p.Leu242=)
11g.46894599C>GCA474204864LRP4c.1530G>C (p.Leu510=)
c.1743G>C (p.Leu581=)
c.726G>C (p.Leu242=)
11g.46894599C>TCA474204865LRP4c.1530G>A (p.Leu510=)
c.1743G>A (p.Leu581=)
c.726G>A (p.Leu242=)
11g.46894600A>CCA380284960LRP4c.1529T>G (p.Leu510Arg)
c.1742T>G (p.Leu581Arg)
c.725T>G (p.Leu242Arg)
11g.46894600A>GCA380284961LRP4c.1529T>C (p.Leu510Pro)
c.1742T>C (p.Leu581Pro)
c.725T>C (p.Leu242Pro)
11g.46894600A>TCA380284962LRP4c.1529T>A (p.Leu510Gln)
c.1742T>A (p.Leu581Gln)
c.725T>A (p.Leu242Gln)
11g.46894601G>ACA474204867LRP4c.1528C>T (p.Leu510=)
c.1741C>T (p.Leu581=)
c.724C>T (p.Leu242=)
 dbSNP gnomAD v2 gnomAD v4
11g.46894601G>CCA380284966LRP4c.1528C>G (p.Leu510Val)
c.1741C>G (p.Leu581Val)
c.724C>G (p.Leu242Val)
11g.46894601G=CA1969144654LRP4c.1528C= (p.Leu510=)
c.1741C= (p.Leu581=)
c.724C= (p.Leu242=)
11g.46894601G>TCA380284968LRP4c.1528C>A (p.Leu510Met)
c.1741C>A (p.Leu581Met)
c.724C>A (p.Leu242Met)
11g.46894602C>ACA474204870LRP4c.1527G>T (p.Gly509=)
c.1740G>T (p.Gly580=)
c.723G>T (p.Gly241=)
11g.46894602C=CA1969144658LRP4c.1527G= (p.Gly509=)
c.1740G= (p.Gly580=)
c.723G= (p.Gly241=)
11g.46894602C>GCA474204868LRP4c.1527G>C (p.Gly509=)
c.1740G>C (p.Gly580=)
c.723G>C (p.Gly241=)
11g.46894602C>TCA474204871LRP4c.1527G>A (p.Gly509=)
c.1740G>A (p.Gly580=)
c.723G>A (p.Gly241=)
 dbSNP gnomAD v2
11g.46894602_46894605delCA2613349859LRP4c.1524_1527del (p.Gly509TrpfsTer?)
c.1737_1740del (p.Gly580TrpfsTer?)
c.720_723del (p.Gly241TrpfsTer?)
 gnomAD v4
11g.46894603C>ACA380284976LRP4c.1526G>T (p.Gly509Val)
c.1739G>T (p.Gly580Val)
c.722G>T (p.Gly241Val)
11g.46894603C>GCA380284971LRP4c.1526G>C (p.Gly509Ala)
c.1739G>C (p.Gly580Ala)
c.722G>C (p.Gly241Ala)
11g.46894603C>TCA380284973LRP4c.1526G>A (p.Gly509Glu)
c.1739G>A (p.Gly580Glu)
c.722G>A (p.Gly241Glu)
11g.46894604C>ACA380284978LRP4c.1525G>T (p.Gly509Trp)
c.1738G>T (p.Gly580Trp)
c.721G>T (p.Gly241Trp)
11g.46894604C>GCA380284979LRP4c.1525G>C (p.Gly509Arg)
c.1738G>C (p.Gly580Arg)
c.721G>C (p.Gly241Arg)
11g.46894604C>TCA380284981LRP4c.1525G>A (p.Gly509Arg)
c.1738G>A (p.Gly580Arg)
c.721G>A (p.Gly241Arg)
11g.46894605A=CA1969144661LRP4c.1524T= (p.Thr508=)
c.1737T= (p.Thr579=)
c.720T= (p.Thr240=)
11g.46894605A>CCA474204872LRP4c.1524T>G (p.Thr508=)
c.1737T>G (p.Thr579=)
c.720T>G (p.Thr240=)
11g.46894605A>GCA474204874LRP4c.1524T>C (p.Thr508=)
c.1737T>C (p.Thr579=)
c.720T>C (p.Thr240=)
 dbSNP gnomAD v2 gnomAD v4
11g.46894605A>TCA474204876LRP4c.1524T>A (p.Thr508=)
c.1737T>A (p.Thr579=)
c.720T>A (p.Thr240=)
11g.46894606G>ACA380284983LRP4c.1523C>T (p.Thr508Ile)
c.1736C>T (p.Thr579Ile)
c.719C>T (p.Thr240Ile)
 gnomAD v4
11g.46894606G>CCA380284985LRP4c.1523C>G (p.Thr508Ser)
c.1736C>G (p.Thr579Ser)
c.719C>G (p.Thr240Ser)
11g.46894606G>TCA380284987LRP4c.1523C>A (p.Thr508Asn)
c.1736C>A (p.Thr579Asn)
c.719C>A (p.Thr240Asn)
11g.46894607T>ACA380284990LRP4c.1522A>T (p.Thr508Ser)
c.1735A>T (p.Thr579Ser)
c.718A>T (p.Thr240Ser)
11g.46894607T>CCA5970129LRP4c.1522A>G (p.Thr508Ala)
c.1735A>G (p.Thr579Ala)
c.718A>G (p.Thr240Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894607T>GCA380284993LRP4c.1522A>C (p.Thr508Pro)
c.1735A>C (p.Thr579Pro)
c.718A>C (p.Thr240Pro)
 gnomAD v4
11g.46894607T=CA1969144666LRP4c.1522A= (p.Thr508=)
c.1735A= (p.Thr579=)
c.718A= (p.Thr240=)
11g.46894608A>CCA474204880LRP4c.1521T>G (p.Ser507=)
c.1734T>G (p.Ser578=)
c.717T>G (p.Ser239=)
11g.46894608A>GCA474204878LRP4c.1521T>C (p.Ser507=)
c.1734T>C (p.Ser578=)
c.717T>C (p.Ser239=)
11g.46894608A>TCA474204879LRP4c.1521T>A (p.Ser507=)
c.1734T>A (p.Ser578=)
c.717T>A (p.Ser239=)
11g.46894609G>ACA380284996LRP4c.1520C>T (p.Ser507Phe)
c.1733C>T (p.Ser578Phe)
c.716C>T (p.Ser239Phe)
11g.46894609G>CCA380284997LRP4c.1520C>G (p.Ser507Cys)
c.1733C>G (p.Ser578Cys)
c.716C>G (p.Ser239Cys)
11g.46894609G>TCA380284999LRP4c.1520C>A (p.Ser507Tyr)
c.1733C>A (p.Ser578Tyr)
c.716C>A (p.Ser239Tyr)
11g.46894610A>CCA380285000LRP4c.1519T>G (p.Ser507Ala)
c.1732T>G (p.Ser578Ala)
c.715T>G (p.Ser239Ala)
11g.46894610A>GCA380285003LRP4c.1519T>C (p.Ser507Pro)
c.1732T>C (p.Ser578Pro)
c.715T>C (p.Ser239Pro)
11g.46894610A>TCA380285001LRP4c.1519T>A (p.Ser507Thr)
c.1732T>A (p.Ser578Thr)
c.715T>A (p.Ser239Thr)
11g.46894611C>ACA474204882LRP4c.1518G>T (p.Val506=)
c.1731G>T (p.Val577=)
c.714G>T (p.Val238=)
11g.46894611C>GCA474204883LRP4c.1518G>C (p.Val506=)
c.1731G>C (p.Val577=)
c.714G>C (p.Val238=)
11g.46894611C>TCA474204884LRP4c.1518G>A (p.Val506=)
c.1731G>A (p.Val577=)
c.714G>A (p.Val238=)
 gnomAD v4
11g.46894612A>CCA380285006LRP4c.1517T>G (p.Val506Gly)
c.1730T>G (p.Val577Gly)
c.713T>G (p.Val238Gly)
11g.46894612A>GCA380285012LRP4c.1517T>C (p.Val506Ala)
c.1730T>C (p.Val577Ala)
c.713T>C (p.Val238Ala)
11g.46894612A>TCA380285009LRP4c.1517T>A (p.Val506Glu)
c.1730T>A (p.Val577Glu)
c.713T>A (p.Val238Glu)
11g.46894613C>ACA380285014LRP4c.1516G>T (p.Val506Leu)
c.1729G>T (p.Val577Leu)
c.712G>T (p.Val238Leu)
11g.46894613C=CA1969144669LRP4c.1516G= (p.Val506=)
c.1729G= (p.Val577=)
c.712G= (p.Val238=)
11g.46894613C>GCA380285030LRP4c.1516G>C (p.Val506Leu)
c.1729G>C (p.Val577Leu)
c.712G>C (p.Val238Leu)
 dbSNP gnomAD v3 gnomAD v4
11g.46894613C>TCA380285027LRP4c.1516G>A (p.Val506Met)
c.1729G>A (p.Val577Met)
c.712G>A (p.Val238Met)
11g.46894614A>CCA474204888LRP4c.1515T>G (p.Val505=)
c.1728T>G (p.Val576=)
c.711T>G (p.Val237=)
11g.46894614A>GCA474204886LRP4c.1515T>C (p.Val505=)
c.1728T>C (p.Val576=)
c.711T>C (p.Val237=)
11g.46894614A>TCA474204887LRP4c.1515T>A (p.Val505=)
c.1728T>A (p.Val576=)
c.711T>A (p.Val237=)
11g.46894615A=CA1969144671LRP4c.1514T= (p.Val505=)
c.1727T= (p.Val576=)
c.710T= (p.Val237=)
11g.46894615A>CCA380285032LRP4c.1514T>G (p.Val505Gly)
c.1727T>G (p.Val576Gly)
c.710T>G (p.Val237Gly)
 dbSNP
11g.46894615A>GCA380285035LRP4c.1514T>C (p.Val505Ala)
c.1727T>C (p.Val576Ala)
c.710T>C (p.Val237Ala)
11g.46894615A>TCA380285038LRP4c.1514T>A (p.Val505Asp)
c.1727T>A (p.Val576Asp)
c.710T>A (p.Val237Asp)
11g.46894616C>ACA380285043LRP4c.1513G>T (p.Val505Phe)
c.1726G>T (p.Val576Phe)
c.709G>T (p.Val237Phe)
11g.46894616C>GCA380285045LRP4c.1513G>C (p.Val505Leu)
c.1726G>C (p.Val576Leu)
c.709G>C (p.Val237Leu)
11g.46894616C>TCA380285048LRP4c.1513G>A (p.Val505Ile)
c.1726G>A (p.Val576Ile)
c.709G>A (p.Val237Ile)
 gnomAD v4
11g.46894617C>ACA380285052LRP4c.1512G>T (p.Glu504Asp)
c.1725G>T (p.Glu575Asp)
c.708G>T (p.Glu236Asp)
11g.46894617C=CA1969144674LRP4c.1512G= (p.Glu504=)
c.1725G= (p.Glu575=)
c.708G= (p.Glu236=)
11g.46894617C>GCA380285054LRP4c.1512G>C (p.Glu504Asp)
c.1725G>C (p.Glu575Asp)
c.708G>C (p.Glu236Asp)
11g.46894617C>TCA474204892LRP4c.1512G>A (p.Glu504=)
c.1725G>A (p.Glu575=)
c.708G>A (p.Glu236=)
 dbSNP
11g.46894618T>ACA380285057LRP4c.1511A>T (p.Glu504Val)
c.1724A>T (p.Glu575Val)
c.707A>T (p.Glu236Val)
11g.46894618T>CCA380285059LRP4c.1511A>G (p.Glu504Gly)
c.1724A>G (p.Glu575Gly)
c.707A>G (p.Glu236Gly)
11g.46894618T>GCA380285062LRP4c.1511A>C (p.Glu504Ala)
c.1724A>C (p.Glu575Ala)
c.707A>C (p.Glu236Ala)
11g.46894619C>ACA380285066LRP4c.1510G>T (p.Glu504Ter)
c.1723G>T (p.Glu575Ter)
c.706G>T (p.Glu236Ter)
11g.46894619C=CA1969144683LRP4c.1510G= (p.Glu504=)
c.1723G= (p.Glu575=)
c.706G= (p.Glu236=)
11g.46894619C>GCA380285073LRP4c.1510G>C (p.Glu504Gln)
c.1723G>C (p.Glu575Gln)
c.706G>C (p.Glu236Gln)
11g.46894619C>TCA5970130LRP4c.1510G>A (p.Glu504Lys)
c.1723G>A (p.Glu575Lys)
c.706G>A (p.Glu236Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894620C>ACA380285076LRP4c.1509G>T (p.Glu503Asp)
c.1722G>T (p.Glu574Asp)
c.705G>T (p.Glu235Asp)
11g.46894620C=CA1969144689LRP4c.1509G= (p.Glu503=)
c.1722G= (p.Glu574=)
c.705G= (p.Glu235=)
11g.46894620C>GCA380285078LRP4c.1509G>C (p.Glu503Asp)
c.1722G>C (p.Glu574Asp)
c.705G>C (p.Glu235Asp)
11g.46894620C>TCA5970131LRP4c.1509G>A (p.Glu503=)
c.1722G>A (p.Glu574=)
c.705G>A (p.Glu235=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894621T>ACA380285081LRP4c.1508A>T (p.Glu503Val)
c.1721A>T (p.Glu574Val)
c.704A>T (p.Glu235Val)
11g.46894621T>CCA380285083LRP4c.1508A>G (p.Glu503Gly)
c.1721A>G (p.Glu574Gly)
c.704A>G (p.Glu235Gly)
11g.46894621T>GCA380285086LRP4c.1508A>C (p.Glu503Ala)
c.1721A>C (p.Glu574Ala)
c.704A>C (p.Glu235Ala)
11g.46894622C>ACA380285089LRP4c.1507G>T (p.Glu503Ter)
c.1720G>T (p.Glu574Ter)
c.703G>T (p.Glu235Ter)
11g.46894622C>GCA380285092LRP4c.1507G>C (p.Glu503Gln)
c.1720G>C (p.Glu574Gln)
c.703G>C (p.Glu235Gln)
11g.46894622C>TCA380285094LRP4c.1507G>A (p.Glu503Lys)
c.1720G>A (p.Glu574Lys)
c.703G>A (p.Glu235Lys)
 gnomAD v4
11g.46894623C>ACA474204897LRP4c.1506G>T (p.Val502=)
c.1719G>T (p.Val573=)
c.702G>T (p.Val234=)
11g.46894623C>GCA474204898LRP4c.1506G>C (p.Val502=)
c.1719G>C (p.Val573=)
c.702G>C (p.Val234=)
11g.46894623C>TCA474204900LRP4c.1506G>A (p.Val502=)
c.1719G>A (p.Val573=)
c.702G>A (p.Val234=)
11g.46894624A>CCA380285099LRP4c.1505T>G (p.Val502Gly)
c.1718T>G (p.Val573Gly)
c.701T>G (p.Val234Gly)
11g.46894624A>GCA380285102LRP4c.1505T>C (p.Val502Ala)
c.1718T>C (p.Val573Ala)
c.701T>C (p.Val234Ala)
11g.46894624A>TCA380285097LRP4c.1505T>A (p.Val502Glu)
c.1718T>A (p.Val573Glu)
c.701T>A (p.Val234Glu)
11g.46894625C>ACA380285105LRP4c.1504G>T (p.Val502Leu)
c.1717G>T (p.Val573Leu)
c.700G>T (p.Val234Leu)
11g.46894625C=CA1969144691LRP4c.1504G= (p.Val502=)
c.1717G= (p.Val573=)
c.700G= (p.Val234=)
11g.46894625C>GCA380285107LRP4c.1504G>C (p.Val502Leu)
c.1717G>C (p.Val573Leu)
c.700G>C (p.Val234Leu)
11g.46894625C>TCA380285110LRP4c.1504G>A (p.Val502Met)
c.1717G>A (p.Val573Met)
c.700G>A (p.Val234Met)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894626G>ACA5970132LRP4c.1503C>T (p.Asn501=)
c.1716C>T (p.Asn572=)
c.699C>T (p.Asn233=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894626G>CCA380285114LRP4c.1503C>G (p.Asn501Lys)
c.1716C>G (p.Asn572Lys)
c.699C>G (p.Asn233Lys)
11g.46894626G=CA1969144695LRP4c.1503C= (p.Asn501=)
c.1716C= (p.Asn572=)
c.699C= (p.Asn233=)
11g.46894626G>TCA380285116LRP4c.1503C>A (p.Asn501Lys)
c.1716C>A (p.Asn572Lys)
c.699C>A (p.Asn233Lys)
11g.46894627T>ACA380285120LRP4c.1502A>T (p.Asn501Ile)
c.1715A>T (p.Asn572Ile)
c.698A>T (p.Asn233Ile)
11g.46894627T>CCA380285123LRP4c.1502A>G (p.Asn501Ser)
c.1715A>G (p.Asn572Ser)
c.698A>G (p.Asn233Ser)
11g.46894627T>GCA380285126LRP4c.1502A>C (p.Asn501Thr)
c.1715A>C (p.Asn572Thr)
c.698A>C (p.Asn233Thr)
11g.46894628T>ACA380285130LRP4c.1501A>T (p.Asn501Tyr)
c.1714A>T (p.Asn572Tyr)
c.697A>T (p.Asn233Tyr)
11g.46894628T>CCA380285138LRP4c.1501A>G (p.Asn501Asp)
c.1714A>G (p.Asn572Asp)
c.697A>G (p.Asn233Asp)
 gnomAD v4
11g.46894628T>GCA5970133LRP4c.1501A>C (p.Asn501His)
c.1714A>C (p.Asn572His)
c.697A>C (p.Asn233His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894628T=CA1969144698LRP4c.1501A= (p.Asn501=)
c.1714A= (p.Asn572=)
c.697A= (p.Asn233=)
11g.46894629G>ACA5970134LRP4c.1500C>T (p.Ser500=)
c.1713C>T (p.Ser571=)
c.696C>T (p.Ser232=)
 dbSNP ExAC gnomAD v4
11g.46894629G>CCA380285142LRP4c.1500C>G (p.Ser500Arg)
c.1713C>G (p.Ser571Arg)
c.696C>G (p.Ser232Arg)
 dbSNP
11g.46894629G=CA1969144708LRP4c.1500C= (p.Ser500=)
c.1713C= (p.Ser571=)
c.696C= (p.Ser232=)
11g.46894629G>TCA380285145LRP4c.1500C>A (p.Ser500Arg)
c.1713C>A (p.Ser571Arg)
c.696C>A (p.Ser232Arg)
11g.46894630C>ACA380285148LRP4c.1499G>T (p.Ser500Ile)
c.1712G>T (p.Ser571Ile)
c.695G>T (p.Ser232Ile)
11g.46894630C=CA1969144711LRP4c.1499G= (p.Ser500=)
c.1712G= (p.Ser571=)
c.695G= (p.Ser232=)
11g.46894630C>GCA380285149LRP4c.1499G>C (p.Ser500Thr)
c.1712G>C (p.Ser571Thr)
c.695G>C (p.Ser232Thr)
11g.46894630C>TCA5970135LRP4c.1499G>A (p.Ser500Asn)
c.1712G>A (p.Ser571Asn)
c.695G>A (p.Ser232Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894631T>ACA380285151LRP4c.1498A>T (p.Ser500Cys)
c.1711A>T (p.Ser571Cys)
c.694A>T (p.Ser232Cys)
11g.46894631T>CCA380285152LRP4c.1498A>G (p.Ser500Gly)
c.1711A>G (p.Ser571Gly)
c.694A>G (p.Ser232Gly)
 dbSNP gnomAD v3 gnomAD v4
11g.46894631T>GCA380285154LRP4c.1498A>C (p.Ser500Arg)
c.1711A>C (p.Ser571Arg)
c.694A>C (p.Ser232Arg)
11g.46894631T=CA1969144713LRP4c.1498A= (p.Ser500=)
c.1711A= (p.Ser571=)
c.694A= (p.Ser232=)
11g.46894632delCA2613349903LRP4c.1497del (p.Ser500AlafsTer?)
c.1710del (p.Ser571AlafsTer?)
c.693del (p.Ser232AlafsTer?)
 gnomAD v4
11g.46894632G>ACA474204904LRP4c.1497C>T (p.Gly499=)
c.1710C>T (p.Gly570=)
c.693C>T (p.Gly231=)
 dbSNP gnomAD v4
11g.46894632G>CCA474204905LRP4c.1497C>G (p.Gly499=)
c.1710C>G (p.Gly570=)
c.693C>G (p.Gly231=)
11g.46894632G=CA1969144715LRP4c.1497C= (p.Gly499=)
c.1710C= (p.Gly570=)
c.693C= (p.Gly231=)
11g.46894632G>TCA474204907LRP4c.1497C>A (p.Gly499=)
c.1710C>A (p.Gly570=)
c.693C>A (p.Gly231=)
11g.46894633C>ACA380285156LRP4c.1496G>T (p.Gly499Val)
c.1709G>T (p.Gly570Val)
c.692G>T (p.Gly231Val)
11g.46894633C>GCA380285159LRP4c.1496G>C (p.Gly499Ala)
c.1709G>C (p.Gly570Ala)
c.692G>C (p.Gly231Ala)
11g.46894633C>TCA380285161LRP4c.1496G>A (p.Gly499Asp)
c.1709G>A (p.Gly570Asp)
c.692G>A (p.Gly231Asp)
 COSMIC
11g.46894634C>ACA380285162LRP4c.1495G>T (p.Gly499Cys)
c.1708G>T (p.Gly570Cys)
c.691G>T (p.Gly231Cys)
11g.46894634C=CA1969144717LRP4c.1495G= (p.Gly499=)
c.1708G= (p.Gly570=)
c.691G= (p.Gly231=)
11g.46894634C>GCA380285165LRP4c.1495G>C (p.Gly499Arg)
c.1708G>C (p.Gly570Arg)
c.691G>C (p.Gly231Arg)
11g.46894634C>TCA5970136LRP4c.1495G>A (p.Gly499Ser)
c.1708G>A (p.Gly570Ser)
c.691G>A (p.Gly231Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894635G>ACA5970137LRP4c.1494C>T (p.Asn498=)
c.1707C>T (p.Asn569=)
c.690C>T (p.Asn230=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894635G>CCA380285175LRP4c.1494C>G (p.Asn498Lys)
c.1707C>G (p.Asn569Lys)
c.690C>G (p.Asn230Lys)
11g.46894635G=CA1969144721LRP4c.1494C= (p.Asn498=)
c.1707C= (p.Asn569=)
c.690C= (p.Asn230=)
11g.46894635G>TCA380285170LRP4c.1494C>A (p.Asn498Lys)
c.1707C>A (p.Asn569Lys)
c.690C>A (p.Asn230Lys)
 dbSNP gnomAD v2 gnomAD v4
11g.46894636T>ACA380285185LRP4c.1493A>T (p.Asn498Ile)
c.1706A>T (p.Asn569Ile)
c.689A>T (p.Asn230Ile)
11g.46894636T>CCA380285179LRP4c.1493A>G (p.Asn498Ser)
c.1706A>G (p.Asn569Ser)
c.689A>G (p.Asn230Ser)
 dbSNP
11g.46894636T>GCA380285182LRP4c.1493A>C (p.Asn498Thr)
c.1706A>C (p.Asn569Thr)
c.689A>C (p.Asn230Thr)
11g.46894636T=CA1969144726LRP4c.1493A= (p.Asn498=)
c.1706A= (p.Asn569=)
c.689A= (p.Asn230=)
11g.46894637T>ACA380285198LRP4c.1492A>T (p.Asn498Tyr)
c.1705A>T (p.Asn569Tyr)
c.688A>T (p.Asn230Tyr)
 gnomAD v4
11g.46894637T>CCA380285200LRP4c.1492A>G (p.Asn498Asp)
c.1705A>G (p.Asn569Asp)
c.688A>G (p.Asn230Asp)
 gnomAD v4
11g.46894637T>GCA5970138LRP4c.1492A>C (p.Asn498His)
c.1705A>C (p.Asn569His)
c.688A>C (p.Asn230His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894637T=CA1969144731LRP4c.1492A= (p.Asn498=)
c.1705A= (p.Asn569=)
c.688A= (p.Asn230=)
11g.46894638G>ACA5970139LRP4c.1491C>T (p.Leu497=)
c.1704C>T (p.Leu568=)
c.687C>T (p.Leu229=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894638G>CCA474204909LRP4c.1491C>G (p.Leu497=)
c.1704C>G (p.Leu568=)
c.687C>G (p.Leu229=)
11g.46894638G=CA1969144738LRP4c.1491C= (p.Leu497=)
c.1704C= (p.Leu568=)
c.687C= (p.Leu229=)
11g.46894638G>TCA474204910LRP4c.1491C>A (p.Leu497=)
c.1704C>A (p.Leu568=)
c.687C>A (p.Leu229=)
11g.46894639A=CA1969144743LRP4c.1490T= (p.Leu497=)
c.1703T= (p.Leu568=)
c.686T= (p.Leu229=)
11g.46894639A>CCA380285208LRP4c.1490T>G (p.Leu497Arg)
c.1703T>G (p.Leu568Arg)
c.686T>G (p.Leu229Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894639A>GCA380285211LRP4c.1490T>C (p.Leu497Pro)
c.1703T>C (p.Leu568Pro)
c.686T>C (p.Leu229Pro)
11g.46894639A>TCA380285214LRP4c.1490T>A (p.Leu497His)
c.1703T>A (p.Leu568His)
c.686T>A (p.Leu229His)
11g.46894640G>ACA380285218LRP4c.1489C>T (p.Leu497Phe)
c.1702C>T (p.Leu568Phe)
c.685C>T (p.Leu229Phe)
11g.46894640G>CCA380285221LRP4c.1489C>G (p.Leu497Val)
c.1702C>G (p.Leu568Val)
c.685C>G (p.Leu229Val)
11g.46894640G>TCA380285224LRP4c.1489C>A (p.Leu497Ile)
c.1702C>A (p.Leu568Ile)
c.685C>A (p.Leu229Ile)
11g.46894641G>ACA5970140LRP4c.1488C>T (p.Asn496=)
c.1701C>T (p.Asn567=)
c.684C>T (p.Asn228=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894641G>CCA380285226LRP4c.1488C>G (p.Asn496Lys)
c.1701C>G (p.Asn567Lys)
c.684C>G (p.Asn228Lys)
11g.46894641G=CA1969144745LRP4c.1488C= (p.Asn496=)
c.1701C= (p.Asn567=)
c.684C= (p.Asn228=)
11g.46894641G>TCA380285230LRP4c.1488C>A (p.Asn496Lys)
c.1701C>A (p.Asn567Lys)
c.684C>A (p.Asn228Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894642T>ACA380285234LRP4c.1487A>T (p.Asn496Ile)
c.1700A>T (p.Asn567Ile)
c.683A>T (p.Asn228Ile)
 dbSNP gnomAD v2 gnomAD v4
11g.46894642T>CCA5970142LRP4c.1487A>G (p.Asn496Ser)
c.1700A>G (p.Asn567Ser)
c.683A>G (p.Asn228Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894642T>GCA5970141LRP4c.1487A>C (p.Asn496Thr)
c.1700A>C (p.Asn567Thr)
c.683A>C (p.Asn228Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894642T=CA1969144753LRP4c.1487A= (p.Asn496=)
c.1700A= (p.Asn567=)
c.683A= (p.Asn228=)
11g.46894643T>ACA380285241LRP4c.1486A>T (p.Asn496Tyr)
c.1699A>T (p.Asn567Tyr)
c.682A>T (p.Asn228Tyr)
11g.46894643T>CCA380285243LRP4c.1486A>G (p.Asn496Asp)
c.1699A>G (p.Asn567Asp)
c.682A>G (p.Asn228Asp)
 gnomAD v4
11g.46894643T>GCA380285247LRP4c.1486A>C (p.Asn496His)
c.1699A>C (p.Asn567His)
c.682A>C (p.Asn228His)
11g.46894644G>ACA474204913LRP4c.1485C>T (p.Ala495=)
c.1698C>T (p.Ala566=)
c.681C>T (p.Ala227=)
11g.46894644G>CCA474204915LRP4c.1485C>G (p.Ala495=)
c.1698C>G (p.Ala566=)
c.681C>G (p.Ala227=)
11g.46894644G>TCA474204916LRP4c.1485C>A (p.Ala495=)
c.1698C>A (p.Ala566=)
c.681C>A (p.Ala227=)
11g.46894645G>ACA380285250LRP4c.1484C>T (p.Ala495Val)
c.1697C>T (p.Ala566Val)
c.680C>T (p.Ala227Val)
 gnomAD v4
11g.46894645G>CCA380285253LRP4c.1484C>G (p.Ala495Gly)
c.1697C>G (p.Ala566Gly)
c.680C>G (p.Ala227Gly)
11g.46894645G>TCA380285256LRP4c.1484C>A (p.Ala495Asp)
c.1697C>A (p.Ala566Asp)
c.680C>A (p.Ala227Asp)
11g.46894646C>ACA380285260LRP4c.1483G>T (p.Ala495Ser)
c.1696G>T (p.Ala566Ser)
c.679G>T (p.Ala227Ser)
11g.46894646C>GCA380285263LRP4c.1483G>C (p.Ala495Pro)
c.1696G>C (p.Ala566Pro)
c.679G>C (p.Ala227Pro)
11g.46894646C>TCA380285265LRP4c.1483G>A (p.Ala495Thr)
c.1696G>A (p.Ala566Thr)
c.679G>A (p.Ala227Thr)
11g.46894647A>CCA474204917LRP4c.1482T>G (p.Arg494=)
c.1695T>G (p.Arg565=)
c.678T>G (p.Arg226=)
11g.46894647A>GCA474204920LRP4c.1482T>C (p.Arg494=)
c.1695T>C (p.Arg565=)
c.678T>C (p.Arg226=)
11g.46894647A>TCA474204918LRP4c.1482T>A (p.Arg494=)
c.1695T>A (p.Arg565=)
c.678T>A (p.Arg226=)
11g.46894648C>ACA380285267LRP4c.1481G>T (p.Arg494Leu)
c.1694G>T (p.Arg565Leu)
c.677G>T (p.Arg226Leu)
 gnomAD v4
11g.46894648C=CA1969144754LRP4c.1481G= (p.Arg494=)
c.1694G= (p.Arg565=)
c.677G= (p.Arg226=)
11g.46894648C>GCA380285269LRP4c.1481G>C (p.Arg494Pro)
c.1694G>C (p.Arg565Pro)
c.677G>C (p.Arg226Pro)
11g.46894648C>TCA5970143LRP4c.1481G>A (p.Arg494His)
c.1694G>A (p.Arg565His)
c.677G>A (p.Arg226His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894649G>ACA5970144LRP4c.1480C>T (p.Arg494Cys)
c.1693C>T (p.Arg565Cys)
c.676C>T (p.Arg226Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894649G>CCA380285271LRP4c.1480C>G (p.Arg494Gly)
c.1693C>G (p.Arg565Gly)
c.676C>G (p.Arg226Gly)
11g.46894649G=CA1969144757LRP4c.1480C= (p.Arg494=)
c.1693C= (p.Arg565=)
c.676C= (p.Arg226=)
11g.46894649G>TCA380285273LRP4c.1480C>A (p.Arg494Ser)
c.1693C>A (p.Arg565Ser)
c.676C>A (p.Arg226Ser)
11g.46894650G>ACA474204921LRP4c.1479C>T (p.Leu493=)
c.1692C>T (p.Leu564=)
c.675C>T (p.Leu225=)
 gnomAD v4
11g.46894650G>CCA474204924LRP4c.1479C>G (p.Leu493=)
c.1692C>G (p.Leu564=)
c.675C>G (p.Leu225=)
11g.46894650G>TCA474204925LRP4c.1479C>A (p.Leu493=)
c.1692C>A (p.Leu564=)
c.675C>A (p.Leu225=)
 COSMIC
11g.46894651A>CCA380285275LRP4c.1478T>G (p.Leu493Arg)
c.1691T>G (p.Leu564Arg)
c.674T>G (p.Leu225Arg)
11g.46894651A>GCA380285277LRP4c.1478T>C (p.Leu493Pro)
c.1691T>C (p.Leu564Pro)
c.674T>C (p.Leu225Pro)
11g.46894651A>TCA380285279LRP4c.1478T>A (p.Leu493His)
c.1691T>A (p.Leu564His)
c.674T>A (p.Leu225His)
11g.46894652G>ACA380285281LRP4c.1477C>T (p.Leu493Phe)
c.1690C>T (p.Leu564Phe)
c.673C>T (p.Leu225Phe)
 dbSNP
11g.46894652G>CCA380285283LRP4c.1477C>G (p.Leu493Val)
c.1690C>G (p.Leu564Val)
c.673C>G (p.Leu225Val)
11g.46894652G=CA1969144763LRP4c.1477C= (p.Leu493=)
c.1690C= (p.Leu564=)
c.673C= (p.Leu225=)
11g.46894652G>TCA380285285LRP4c.1477C>A (p.Leu493Ile)
c.1690C>A (p.Leu564Ile)
c.673C>A (p.Leu225Ile)
11g.46894653G>ACA474204929LRP4c.1476C>T (p.Ile492=)
c.1689C>T (p.Ile563=)
c.672C>T (p.Ile224=)
11g.46894653G>CCA380285287LRP4c.1476C>G (p.Ile492Met)
c.1689C>G (p.Ile563Met)
c.672C>G (p.Ile224Met)
11g.46894653G>TCA474204930LRP4c.1476C>A (p.Ile492=)
c.1689C>A (p.Ile563=)
c.672C>A (p.Ile224=)
11g.46894654A>CCA380285289LRP4c.1475T>G (p.Ile492Ser)
c.1688T>G (p.Ile563Ser)
c.671T>G (p.Ile224Ser)
11g.46894654A>GCA380285291LRP4c.1475T>C (p.Ile492Thr)
c.1688T>C (p.Ile563Thr)
c.671T>C (p.Ile224Thr)
11g.46894654A>TCA380285293LRP4c.1475T>A (p.Ile492Asn)
c.1688T>A (p.Ile563Asn)
c.671T>A (p.Ile224Asn)
11g.46894655T>ACA380285297LRP4c.1474A>T (p.Ile492Phe)
c.1687A>T (p.Ile563Phe)
c.670A>T (p.Ile224Phe)
11g.46894655T>CCA380285295LRP4c.1474A>G (p.Ile492Val)
c.1687A>G (p.Ile563Val)
c.670A>G (p.Ile224Val)
 dbSNP gnomAD v3 gnomAD v4
11g.46894655T>GCA380285294LRP4c.1474A>C (p.Ile492Leu)
c.1687A>C (p.Ile563Leu)
c.670A>C (p.Ile224Leu)
11g.46894655T=CA1969144768LRP4c.1474A= (p.Ile492=)
c.1687A= (p.Ile563=)
c.670A= (p.Ile224=)
11g.46894656C>ACA474204936LRP4c.1473G>T (p.Arg491=)
c.1686G>T (p.Arg562=)
c.669G>T (p.Arg223=)
11g.46894656C>GCA474204934LRP4c.1473G>C (p.Arg491=)
c.1686G>C (p.Arg562=)
c.669G>C (p.Arg223=)
11g.46894656C>TCA474204932LRP4c.1473G>A (p.Arg491=)
c.1686G>A (p.Arg562=)
c.669G>A (p.Arg223=)
11g.46894657C>ACA380285298LRP4c.1472G>T (p.Arg491Leu)
c.1685G>T (p.Arg562Leu)
c.668G>T (p.Arg223Leu)
11g.46894657C=CA1969144771LRP4c.1472G= (p.Arg491=)
c.1685G= (p.Arg562=)
c.668G= (p.Arg223=)
11g.46894657C>GCA380285301LRP4c.1472G>C (p.Arg491Pro)
c.1685G>C (p.Arg562Pro)
c.668G>C (p.Arg223Pro)
11g.46894657C>TCA5970145LRP4c.1472G>A (p.Arg491Gln)
c.1685G>A (p.Arg562Gln)
c.668G>A (p.Arg223Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894658G>ACA5970146LRP4c.1471C>T (p.Arg491Trp)
c.1684C>T (p.Arg562Trp)
c.667C>T (p.Arg223Trp)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894658G>CCA380285308LRP4c.1471C>G (p.Arg491Gly)
c.1684C>G (p.Arg562Gly)
c.667C>G (p.Arg223Gly)
11g.46894658G=CA1969144775LRP4c.1471C= (p.Arg491=)
c.1684C= (p.Arg562=)
c.667C= (p.Arg223=)
11g.46894658G>TCA474204937LRP4c.1471C>A (p.Arg491=)
c.1684C>A (p.Arg562=)
c.667C>A (p.Arg223=)
11g.46894659G>ACA474204938LRP4c.1470C>T (p.Asp490=)
c.1683C>T (p.Asp561=)
c.666C>T (p.Asp222=)
11g.46894659G>CCA380285310LRP4c.1470C>G (p.Asp490Glu)
c.1683C>G (p.Asp561Glu)
c.666C>G (p.Asp222Glu)
11g.46894659G>TCA380285317LRP4c.1470C>A (p.Asp490Glu)
c.1683C>A (p.Asp561Glu)
c.666C>A (p.Asp222Glu)
11g.46894660T>ACA380285319LRP4c.1469A>T (p.Asp490Val)
c.1682A>T (p.Asp561Val)
c.665A>T (p.Asp222Val)
11g.46894660T>CCA380285320LRP4c.1469A>G (p.Asp490Gly)
c.1682A>G (p.Asp561Gly)
c.665A>G (p.Asp222Gly)
11g.46894660T>GCA380285324LRP4c.1469A>C (p.Asp490Ala)
c.1682A>C (p.Asp561Ala)
c.665A>C (p.Asp222Ala)
11g.46894661C>ACA380285327LRP4c.1468G>T (p.Asp490Tyr)
c.1681G>T (p.Asp561Tyr)
c.664G>T (p.Asp222Tyr)
 gnomAD v4
11g.46894661C>GCA380285330LRP4c.1468G>C (p.Asp490His)
c.1681G>C (p.Asp561His)
c.664G>C (p.Asp222His)
11g.46894661C>TCA380285331LRP4c.1468G>A (p.Asp490Asn)
c.1681G>A (p.Asp561Asn)
c.664G>A (p.Asp222Asn)
11g.46894662C>ACA474204941LRP4c.1467G>T (p.Leu489=)
c.1680G>T (p.Leu560=)
c.663G>T (p.Leu221=)
11g.46894662C>GCA474204942LRP4c.1467G>C (p.Leu489=)
c.1680G>C (p.Leu560=)
c.663G>C (p.Leu221=)
11g.46894662C>TCA474204944LRP4c.1467G>A (p.Leu489=)
c.1680G>A (p.Leu560=)
c.663G>A (p.Leu221=)
11g.46894663A>CCA380285338LRP4c.1466T>G (p.Leu489Arg)
c.1679T>G (p.Leu560Arg)
c.662T>G (p.Leu221Arg)
11g.46894663A>GCA380285336LRP4c.1466T>C (p.Leu489Pro)
c.1679T>C (p.Leu560Pro)
c.662T>C (p.Leu221Pro)
11g.46894663A>TCA380285334LRP4c.1466T>A (p.Leu489Gln)
c.1679T>A (p.Leu560Gln)
c.662T>A (p.Leu221Gln)
11g.46894663_46894664delinsAGCA1969144779LRP4c.1465_1466delinsCT (p.Leu489=)
c.1678_1679delinsCT (p.Leu560=)
c.661_662delinsCT (p.Leu221=)
11g.46894664G>ACA5970147LRP4c.1465C>T (p.Leu489=)
c.1678C>T (p.Leu560=)
c.661C>T (p.Leu221=)
 dbSNP ExAC gnomAD v2 gnomAD v4
11g.46894664G>CCA380285346LRP4c.1465C>G (p.Leu489Val)
c.1678C>G (p.Leu560Val)
c.661C>G (p.Leu221Val)
11g.46894664G=CA1969144782LRP4c.1465C= (p.Leu489=)
c.1678C= (p.Leu560=)
c.661C= (p.Leu221=)
11g.46894664G>TCA380285343LRP4c.1465C>A (p.Leu489Met)
c.1678C>A (p.Leu560Met)
c.661C>A (p.Leu221Met)
11g.46894666delCA599373008LRP4c.1465del (p.Leu489TrpfsTer?)
c.1678del (p.Leu560TrpfsTer?)
c.661del (p.Leu221TrpfsTer?)
 dbSNP gnomAD v2 gnomAD v4
11g.46894665G>ACA474204947LRP4c.1464C>T (p.Thr488=)
c.1677C>T (p.Thr559=)
c.660C>T (p.Thr220=)
11g.46894665G>CCA474204948LRP4c.1464C>G (p.Thr488=)
c.1677C>G (p.Thr559=)
c.660C>G (p.Thr220=)
 gnomAD v4
11g.46894665G>TCA474204949LRP4c.1464C>A (p.Thr488=)
c.1677C>A (p.Thr559=)
c.660C>A (p.Thr220=)
11g.46894666G>ACA380285350LRP4c.1463C>T (p.Thr488Ile)
c.1676C>T (p.Thr559Ile)
c.659C>T (p.Thr220Ile)
11g.46894666G>CCA380285353LRP4c.1463C>G (p.Thr488Ser)
c.1676C>G (p.Thr559Ser)
c.659C>G (p.Thr220Ser)
11g.46894666G>TCA380285355LRP4c.1463C>A (p.Thr488Asn)
c.1676C>A (p.Thr559Asn)
c.659C>A (p.Thr220Asn)
11g.46894666_46894667insACA2613349968LRP4c.1462_1463insT (p.Thr488IlefsTer?)
c.1675_1676insT (p.Thr559IlefsTer?)
c.658_659insT (p.Thr220IlefsTer?)
 gnomAD v4
11g.46894667T>ACA380285364LRP4c.1462A>T (p.Thr488Ser)
c.1675A>T (p.Thr559Ser)
c.658A>T (p.Thr220Ser)
11g.46894667T>CCA380285366LRP4c.1462A>G (p.Thr488Ala)
c.1675A>G (p.Thr559Ala)
c.658A>G (p.Thr220Ala)
11g.46894667T>GCA380285370LRP4c.1462A>C (p.Thr488Pro)
c.1675A>C (p.Thr559Pro)
c.658A>C (p.Thr220Pro)
 gnomAD v4
11g.46894668G>ACA474204951LRP4c.1461C>T (p.Val487=)
c.1674C>T (p.Val558=)
c.657C>T (p.Val219=)
 ClinVar
11g.46894668G>CCA474204952LRP4c.1461C>G (p.Val487=)
c.1674C>G (p.Val558=)
c.657C>G (p.Val219=)
 gnomAD v4
11g.46894668G>TCA474204953LRP4c.1461C>A (p.Val487=)
c.1674C>A (p.Val558=)
c.657C>A (p.Val219=)
11g.46894669A>CCA380285373LRP4c.1460T>G (p.Val487Gly)
c.1673T>G (p.Val558Gly)
c.656T>G (p.Val219Gly)
11g.46894669A>GCA380285375LRP4c.1460T>C (p.Val487Ala)
c.1673T>C (p.Val558Ala)
c.656T>C (p.Val219Ala)
11g.46894669A>TCA380285378LRP4c.1460T>A (p.Val487Asp)
c.1673T>A (p.Val558Asp)
c.656T>A (p.Val219Asp)
11g.46894670C>ACA380285381LRP4c.1459G>T (p.Val487Phe)
c.1672G>T (p.Val558Phe)
c.655G>T (p.Val219Phe)
11g.46894670C>GCA380285383LRP4c.1459G>C (p.Val487Leu)
c.1672G>C (p.Val558Leu)
c.655G>C (p.Val219Leu)
11g.46894670C>TCA380285384LRP4c.1459G>A (p.Val487Ile)
c.1672G>A (p.Val558Ile)
c.655G>A (p.Val219Ile)
11g.46894671A>CCA380285388LRP4c.1458T>G (p.Asp486Glu)
c.1671T>G (p.Asp557Glu)
c.654T>G (p.Asp218Glu)
11g.46894671A>GCA474204955LRP4c.1458T>C (p.Asp486=)
c.1671T>C (p.Asp557=)
c.654T>C (p.Asp218=)
11g.46894671A>TCA380285390LRP4c.1458T>A (p.Asp486Glu)
c.1671T>A (p.Asp557Glu)
c.654T>A (p.Asp218Glu)
 gnomAD v4
11g.46894672T>ACA380285395LRP4c.1457A>T (p.Asp486Val)
c.1670A>T (p.Asp557Val)
c.653A>T (p.Asp218Val)
11g.46894672T>CCA380285394LRP4c.1457A>G (p.Asp486Gly)
c.1670A>G (p.Asp557Gly)
c.653A>G (p.Asp218Gly)
11g.46894672T>GCA380285393LRP4c.1457A>C (p.Asp486Ala)
c.1670A>C (p.Asp557Ala)
c.653A>C (p.Asp218Ala)
11g.46894673C>ACA380285398LRP4c.1456G>T (p.Asp486Tyr)
c.1669G>T (p.Asp557Tyr)
c.652G>T (p.Asp218Tyr)
11g.46894673C>GCA380285401LRP4c.1456G>C (p.Asp486His)
c.1669G>C (p.Asp557His)
c.652G>C (p.Asp218His)
11g.46894673C>TCA380285404LRP4c.1456G>A (p.Asp486Asn)
c.1669G>A (p.Asp557Asn)
c.652G>A (p.Asp218Asn)
11g.46894674T>ACA474204957LRP4c.1455A>T (p.Ser485=)
c.1668A>T (p.Ser556=)
c.651A>T (p.Ser217=)
11g.46894674T>CCA474204958LRP4c.1455A>G (p.Ser485=)
c.1668A>G (p.Ser556=)
c.651A>G (p.Ser217=)
11g.46894674T>GCA474204959LRP4c.1455A>C (p.Ser485=)
c.1668A>C (p.Ser556=)
c.651A>C (p.Ser217=)
11g.46894675G>ACA380285406LRP4c.1454C>T (p.Ser485Leu)
c.1667C>T (p.Ser556Leu)
c.650C>T (p.Ser217Leu)
11g.46894675G>CCA380285409LRP4c.1454C>G (p.Ser485Ter)
c.1667C>G (p.Ser556Ter)
c.650C>G (p.Ser217Ter)
11g.46894675G>TCA380285412LRP4c.1454C>A (p.Ser485Ter)
c.1667C>A (p.Ser556Ter)
c.650C>A (p.Ser217Ter)
11g.46894676A>CCA380285416LRP4c.1453T>G (p.Ser485Ala)
c.1666T>G (p.Ser556Ala)
c.649T>G (p.Ser217Ala)
11g.46894676A>GCA380285418LRP4c.1453T>C (p.Ser485Pro)
c.1666T>C (p.Ser556Pro)
c.649T>C (p.Ser217Pro)
11g.46894676A>TCA380285421LRP4c.1453T>A (p.Ser485Thr)
c.1666T>A (p.Ser556Thr)
c.649T>A (p.Ser217Thr)
11g.46894677C>ACA380285424LRP4c.1452G>T (p.Trp484Cys)
c.1665G>T (p.Trp555Cys)
c.648G>T (p.Trp216Cys)
11g.46894677C>GCA380285427LRP4c.1452G>C (p.Trp484Cys)
c.1665G>C (p.Trp555Cys)
c.648G>C (p.Trp216Cys)
11g.46894677C>TCA380285429LRP4c.1452G>A (p.Trp484Ter)
c.1665G>A (p.Trp555Ter)
c.648G>A (p.Trp216Ter)
11g.46894678C>ACA380285431LRP4c.1451G>T (p.Trp484Leu)
c.1664G>T (p.Trp555Leu)
c.647G>T (p.Trp216Leu)
11g.46894678C>GCA380285434LRP4c.1451G>C (p.Trp484Ser)
c.1664G>C (p.Trp555Ser)
c.647G>C (p.Trp216Ser)
11g.46894678C>TCA380285435LRP4c.1451G>A (p.Trp484Ter)
c.1664G>A (p.Trp555Ter)
c.647G>A (p.Trp216Ter)
 gnomAD v4
11g.46894679A>CCA380285440LRP4c.1450T>G (p.Trp484Gly)
c.1663T>G (p.Trp555Gly)
c.646T>G (p.Trp216Gly)
11g.46894679A>GCA380285442LRP4c.1450T>C (p.Trp484Arg)
c.1663T>C (p.Trp555Arg)
c.646T>C (p.Trp216Arg)
11g.46894679A>TCA380285439LRP4c.1450T>A (p.Trp484Arg)
c.1663T>A (p.Trp555Arg)
c.646T>A (p.Trp216Arg)
11g.46894680G>ACA474204961LRP4c.1449C>T (p.Phe483=)
c.1662C>T (p.Phe554=)
c.645C>T (p.Phe215=)
11g.46894680G>CCA380285443LRP4c.1449C>G (p.Phe483Leu)
c.1662C>G (p.Phe554Leu)
c.645C>G (p.Phe215Leu)
11g.46894680G>TCA380285445LRP4c.1449C>A (p.Phe483Leu)
c.1662C>A (p.Phe554Leu)
c.645C>A (p.Phe215Leu)
11g.46894681A>CCA380285447LRP4c.1448T>G (p.Phe483Cys)
c.1661T>G (p.Phe554Cys)
c.644T>G (p.Phe215Cys)
11g.46894681A>GCA380285450LRP4c.1448T>C (p.Phe483Ser)
c.1661T>C (p.Phe554Ser)
c.644T>C (p.Phe215Ser)
11g.46894681A>TCA380285452LRP4c.1448T>A (p.Phe483Tyr)
c.1661T>A (p.Phe554Tyr)
c.644T>A (p.Phe215Tyr)
11g.46894682A=CA1969144787LRP4c.1447T= (p.Phe483=)
c.1660T= (p.Phe554=)
c.643T= (p.Phe215=)
11g.46894682A>CCA380285455LRP4c.1447T>G (p.Phe483Val)
c.1660T>G (p.Phe554Val)
c.643T>G (p.Phe215Val)
11g.46894682A>GCA5970148LRP4c.1447T>C (p.Phe483Leu)
c.1660T>C (p.Phe554Leu)
c.643T>C (p.Phe215Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894682A>TCA380285460LRP4c.1447T>A (p.Phe483Ile)
c.1660T>A (p.Phe554Ile)
c.643T>A (p.Phe215Ile)
11g.46894683G>ACA474204963LRP4c.1446C>T (p.Val482=)
c.1659C>T (p.Val553=)
c.642C>T (p.Val214=)
 dbSNP gnomAD v2 gnomAD v4
11g.46894683G>CCA474204964LRP4c.1446C>G (p.Val482=)
c.1659C>G (p.Val553=)
c.642C>G (p.Val214=)
11g.46894683G=CA1969144791LRP4c.1446C= (p.Val482=)
c.1659C= (p.Val553=)
c.642C= (p.Val214=)
11g.46894683G>TCA474204965LRP4c.1446C>A (p.Val482=)
c.1659C>A (p.Val553=)
c.642C>A (p.Val214=)
11g.46894684A>CCA380285463LRP4c.1445T>G (p.Val482Gly)
c.1658T>G (p.Val553Gly)
c.641T>G (p.Val214Gly)
11g.46894684A>GCA380285465LRP4c.1445T>C (p.Val482Ala)
c.1658T>C (p.Val553Ala)
c.641T>C (p.Val214Ala)
11g.46894684A>TCA380285468LRP4c.1445T>A (p.Val482Asp)
c.1658T>A (p.Val553Asp)
c.641T>A (p.Val214Asp)
11g.46894685C>ACA380285471LRP4c.1444G>T (p.Val482Phe)
c.1657G>T (p.Val553Phe)
c.640G>T (p.Val214Phe)
11g.46894685C=CA1969144796LRP4c.1444G= (p.Val482=)
c.1657G= (p.Val553=)
c.640G= (p.Val214=)
11g.46894685C>GCA380285472LRP4c.1444G>C (p.Val482Leu)
c.1657G>C (p.Val553Leu)
c.640G>C (p.Val214Leu)
11g.46894685C>TCA221647359LRP4c.1444G>A (p.Val482Ile)
c.1657G>A (p.Val553Ile)
c.640G>A (p.Val214Ile)
 dbSNP gnomAD v4
11g.46894686A>CCA474204967LRP4c.1443T>G (p.Leu481=)
c.1656T>G (p.Leu552=)
c.639T>G (p.Leu213=)
11g.46894686A>GCA474204969LRP4c.1443T>C (p.Leu481=)
c.1656T>C (p.Leu552=)
c.639T>C (p.Leu213=)
 dbSNP
11g.46894686A>TCA474204970LRP4c.1443T>A (p.Leu481=)
c.1656T>A (p.Leu552=)
c.639T>A (p.Leu213=)
11g.46894687A>CCA380285484LRP4c.1442T>G (p.Leu481Arg)
c.1655T>G (p.Leu552Arg)
c.638T>G (p.Leu213Arg)
11g.46894687A>GCA380285481LRP4c.1442T>C (p.Leu481Pro)
c.1655T>C (p.Leu552Pro)
c.638T>C (p.Leu213Pro)
11g.46894687A>TCA380285478LRP4c.1442T>A (p.Leu481His)
c.1655T>A (p.Leu552His)
c.638T>A (p.Leu213His)
11g.46894688G>ACA380285487LRP4c.1441C>T (p.Leu481Phe)
c.1654C>T (p.Leu552Phe)
c.637C>T (p.Leu213Phe)
11g.46894688G>CCA380285489LRP4c.1441C>G (p.Leu481Val)
c.1654C>G (p.Leu552Val)
c.637C>G (p.Leu213Val)
11g.46894688G>TCA380285492LRP4c.1441C>A (p.Leu481Ile)
c.1654C>A (p.Leu552Ile)
c.637C>A (p.Leu213Ile)
11g.46894689C>ACA380285496LRP4c.1440G>T (p.Glu480Asp)
c.1653G>T (p.Glu551Asp)
c.636G>T (p.Glu212Asp)
11g.46894689C=CA1969144799LRP4c.1440G= (p.Glu480=)
c.1653G= (p.Glu551=)
c.636G= (p.Glu212=)
11g.46894689C>GCA380285499LRP4c.1440G>C (p.Glu480Asp)
c.1653G>C (p.Glu551Asp)
c.636G>C (p.Glu212Asp)
 gnomAD v4
11g.46894689C>TCA474204972LRP4c.1440G>A (p.Glu480=)
c.1653G>A (p.Glu551=)
c.636G>A (p.Glu212=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.46894690T>ACA380285503LRP4c.1439A>T (p.Glu480Val)
c.1652A>T (p.Glu551Val)
c.635A>T (p.Glu212Val)
11g.46894690T>CCA380285506LRP4c.1439A>G (p.Glu480Gly)
c.1652A>G (p.Glu551Gly)
c.635A>G (p.Glu212Gly)
11g.46894690T>GCA380285510LRP4c.1439A>C (p.Glu480Ala)
c.1652A>C (p.Glu551Ala)
c.635A>C (p.Glu212Ala)
11g.46894691C>ACA380285513LRP4c.1438G>T (p.Glu480Ter)
c.1651G>T (p.Glu551Ter)
c.634G>T (p.Glu212Ter)
11g.46894691C=CA1969144805LRP4c.1438G= (p.Glu480=)
c.1651G= (p.Glu551=)
c.634G= (p.Glu212=)
11g.46894691C>GCA5970149LRP4c.1438G>C (p.Glu480Gln)
c.1651G>C (p.Glu551Gln)
c.634G>C (p.Glu212Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894691C>TCA380285516LRP4c.1438G>A (p.Glu480Lys)
c.1651G>A (p.Glu551Lys)
c.634G>A (p.Glu212Lys)
 dbSNP gnomAD v4
11g.46894692G>ACA5970150LRP4c.1437C>T (p.Arg479=)
c.1650C>T (p.Arg550=)
c.633C>T (p.Arg211=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.46894692G>CCA474204973LRP4c.1437C>G (p.Arg479=)
c.1650C>G (p.Arg550=)
c.633C>G (p.Arg211=)
11g.46894692G=CA1969144810LRP4c.1437C= (p.Arg479=)
c.1650C= (p.Arg550=)
c.633C= (p.Arg211=)
11g.46894692G>TCA474204974LRP4c.1437C>A (p.Arg479=)
c.1650C>A (p.Arg550=)
c.633C>A (p.Arg211=)
11g.46894693C>ACA380285523LRP4c.1436G>T (p.Arg479Leu)
c.1649G>T (p.Arg550Leu)
c.632G>T (p.Arg211Leu)
 ClinVar dbSNP gnomAD v4
11g.46894693C=CA1969144814LRP4c.1436G= (p.Arg479=)
c.1649G= (p.Arg550=)
c.632G= (p.Arg211=)
11g.46894693C>GCA380285531LRP4c.1436G>C (p.Arg479Pro)
c.1649G>C (p.Arg550Pro)
c.632G>C (p.Arg211Pro)
11g.46894693C>TCA5970151LRP4c.1436G>A (p.Arg479His)
c.1649G>A (p.Arg550His)
c.632G>A (p.Arg211His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
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)

Number of alleles fetched