Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.25897591T>ACA409806294APPn.2013A>T
n.443A>T
n.712A>T
c.2046A>T (p.Glu682Asp)
c.1821A>T (p.Glu607Asp)
c.1653A>T (p.Glu551Asp)
c.1989A>T (p.Glu663Asp)
c.1992A>T (p.Glu664Asp)
c.1716A>T (p.Glu572Asp)
c.1878A>T (p.Glu626Asp)
c.1974A>T (p.Glu658Asp)
n.393A>T
c.1935A>T (p.Glu645Asp)
c.1767A>T (p.Glu589Asp)
21g.25897591T>CCA511686155APPn.2013A>G
n.443A>G
n.712A>G
c.2046A>G (p.Glu682=)
c.1821A>G (p.Glu607=)
c.1653A>G (p.Glu551=)
c.1989A>G (p.Glu663=)
c.1992A>G (p.Glu664=)
c.1716A>G (p.Glu572=)
c.1878A>G (p.Glu626=)
c.1974A>G (p.Glu658=)
n.393A>G
c.1935A>G (p.Glu645=)
c.1767A>G (p.Glu589=)
 ClinVar dbSNP gnomAD v4
21g.25897591T>GCA409806296APPn.2013A>C
n.443A>C
n.712A>C
c.2046A>C (p.Glu682Asp)
c.1821A>C (p.Glu607Asp)
c.1653A>C (p.Glu551Asp)
c.1989A>C (p.Glu663Asp)
c.1992A>C (p.Glu664Asp)
c.1716A>C (p.Glu572Asp)
c.1878A>C (p.Glu626Asp)
c.1974A>C (p.Glu658Asp)
n.393A>C
c.1935A>C (p.Glu645Asp)
c.1767A>C (p.Glu589Asp)
21g.25897591T=CA2383554910APPn.2013A=
n.443A=
n.712A=
c.2046A= (p.Glu682=)
c.1821A= (p.Glu607=)
c.1653A= (p.Glu551=)
c.1989A= (p.Glu663=)
c.1992A= (p.Glu664=)
c.1716A= (p.Glu572=)
c.1878A= (p.Glu626=)
c.1974A= (p.Glu658=)
n.393A=
c.1935A= (p.Glu645=)
c.1767A= (p.Glu589=)
21g.25897592T>ACA409806298APPn.2012A>T
n.442A>T
n.711A>T
c.2045A>T (p.Glu682Val)
c.1820A>T (p.Glu607Val)
c.1652A>T (p.Glu551Val)
c.1988A>T (p.Glu663Val)
c.1991A>T (p.Glu664Val)
c.1715A>T (p.Glu572Val)
c.1877A>T (p.Glu626Val)
c.1973A>T (p.Glu658Val)
n.392A>T
c.1934A>T (p.Glu645Val)
c.1766A>T (p.Glu589Val)
21g.25897592T>CCA409806300APPn.2012A>G
n.442A>G
n.711A>G
c.2045A>G (p.Glu682Gly)
c.1820A>G (p.Glu607Gly)
c.1652A>G (p.Glu551Gly)
c.1988A>G (p.Glu663Gly)
c.1991A>G (p.Glu664Gly)
c.1715A>G (p.Glu572Gly)
c.1877A>G (p.Glu626Gly)
c.1973A>G (p.Glu658Gly)
n.392A>G
c.1934A>G (p.Glu645Gly)
c.1766A>G (p.Glu589Gly)
21g.25897592T>GCA409806302APPn.2012A>C
n.442A>C
n.711A>C
c.2045A>C (p.Glu682Ala)
c.1820A>C (p.Glu607Ala)
c.1652A>C (p.Glu551Ala)
c.1988A>C (p.Glu663Ala)
c.1991A>C (p.Glu664Ala)
c.1715A>C (p.Glu572Ala)
c.1877A>C (p.Glu626Ala)
c.1973A>C (p.Glu658Ala)
n.392A>C
c.1934A>C (p.Glu645Ala)
c.1766A>C (p.Glu589Ala)
 gnomAD v4
21g.25897593C>ACA409806304APPn.2011G>T
n.441G>T
n.710G>T
c.2044G>T (p.Glu682Ter)
c.1819G>T (p.Glu607Ter)
c.1651G>T (p.Glu551Ter)
c.1987G>T (p.Glu663Ter)
c.1990G>T (p.Glu664Ter)
c.1714G>T (p.Glu572Ter)
c.1876G>T (p.Glu626Ter)
c.1972G>T (p.Glu658Ter)
n.391G>T
c.1933G>T (p.Glu645Ter)
c.1765G>T (p.Glu589Ter)
21g.25897593C=CA2383554911APPn.2011G=
n.441G=
n.710G=
c.2044G= (p.Glu682=)
c.1819G= (p.Glu607=)
c.1651G= (p.Glu551=)
c.1987G= (p.Glu663=)
c.1990G= (p.Glu664=)
c.1714G= (p.Glu572=)
c.1876G= (p.Glu626=)
c.1972G= (p.Glu658=)
n.391G=
c.1933G= (p.Glu645=)
c.1765G= (p.Glu589=)
21g.25897593C>GCA409806306APPn.2011G>C
n.441G>C
n.710G>C
c.2044G>C (p.Glu682Gln)
c.1819G>C (p.Glu607Gln)
c.1651G>C (p.Glu551Gln)
c.1987G>C (p.Glu663Gln)
c.1990G>C (p.Glu664Gln)
c.1714G>C (p.Glu572Gln)
c.1876G>C (p.Glu626Gln)
c.1972G>C (p.Glu658Gln)
n.391G>C
c.1933G>C (p.Glu645Gln)
c.1765G>C (p.Glu589Gln)
 gnomAD v4
21g.25897593C>TCA409806308APPn.2011G>A
n.441G>A
n.710G>A
c.2044G>A (p.Glu682Lys)
c.1819G>A (p.Glu607Lys)
c.1651G>A (p.Glu551Lys)
c.1987G>A (p.Glu663Lys)
c.1990G>A (p.Glu664Lys)
c.1714G>A (p.Glu572Lys)
c.1876G>A (p.Glu626Lys)
c.1972G>A (p.Glu658Lys)
n.391G>A
c.1933G>A (p.Glu645Lys)
c.1765G>A (p.Glu589Lys)
 dbSNP
21g.25897594A>CCA409806310APPn.2010T>G
n.440T>G
n.709T>G
c.2043T>G (p.Tyr681Ter)
c.1818T>G (p.Tyr606Ter)
c.1650T>G (p.Tyr550Ter)
c.1986T>G (p.Tyr662Ter)
c.1989T>G (p.Tyr663Ter)
c.1713T>G (p.Tyr571Ter)
c.1875T>G (p.Tyr625Ter)
c.1971T>G (p.Tyr657Ter)
n.390T>G
c.1932T>G (p.Tyr644Ter)
c.1764T>G (p.Tyr588Ter)
21g.25897594A>GCA511686157APPn.2010T>C
n.440T>C
n.709T>C
c.2043T>C (p.Tyr681=)
c.1818T>C (p.Tyr606=)
c.1650T>C (p.Tyr550=)
c.1986T>C (p.Tyr662=)
c.1989T>C (p.Tyr663=)
c.1713T>C (p.Tyr571=)
c.1875T>C (p.Tyr625=)
c.1971T>C (p.Tyr657=)
n.390T>C
c.1932T>C (p.Tyr644=)
c.1764T>C (p.Tyr588=)
21g.25897594A>TCA409806312APPn.2010T>A
n.440T>A
n.709T>A
c.2043T>A (p.Tyr681Ter)
c.1818T>A (p.Tyr606Ter)
c.1650T>A (p.Tyr550Ter)
c.1986T>A (p.Tyr662Ter)
c.1989T>A (p.Tyr663Ter)
c.1713T>A (p.Tyr571Ter)
c.1875T>A (p.Tyr625Ter)
c.1971T>A (p.Tyr657Ter)
n.390T>A
c.1932T>A (p.Tyr644Ter)
c.1764T>A (p.Tyr588Ter)
21g.25897594dupCA637163687APPn.2010dup
n.440dup
n.709dup
c.2043dup (p.Glu682Ter)
c.1818dup (p.Glu607Ter)
c.1650dup (p.Glu551Ter)
c.1986dup (p.Glu663Ter)
c.1989dup (p.Glu664Ter)
c.1713dup (p.Glu572Ter)
c.1875dup (p.Glu626Ter)
c.1971dup (p.Glu658Ter)
n.390dup
c.1932dup (p.Glu645Ter)
c.1764dup (p.Glu589Ter)
 dbSNP gnomAD v2 gnomAD v4
21g.25897595T>ACA409806314APPn.2009A>T
n.439A>T
n.708A>T
c.2042A>T (p.Tyr681Phe)
c.1817A>T (p.Tyr606Phe)
c.1649A>T (p.Tyr550Phe)
c.1985A>T (p.Tyr662Phe)
c.1988A>T (p.Tyr663Phe)
c.1712A>T (p.Tyr571Phe)
c.1874A>T (p.Tyr625Phe)
c.1970A>T (p.Tyr657Phe)
n.389A>T
c.1931A>T (p.Tyr644Phe)
c.1763A>T (p.Tyr588Phe)
21g.25897595T>CCA409806315APPn.2009A>G
n.439A>G
n.708A>G
c.2042A>G (p.Tyr681Cys)
c.1817A>G (p.Tyr606Cys)
c.1649A>G (p.Tyr550Cys)
c.1985A>G (p.Tyr662Cys)
c.1988A>G (p.Tyr663Cys)
c.1712A>G (p.Tyr571Cys)
c.1874A>G (p.Tyr625Cys)
c.1970A>G (p.Tyr657Cys)
n.389A>G
c.1931A>G (p.Tyr644Cys)
c.1763A>G (p.Tyr588Cys)
21g.25897595T>GCA409806317APPn.2009A>C
n.439A>C
n.708A>C
c.2042A>C (p.Tyr681Ser)
c.1817A>C (p.Tyr606Ser)
c.1649A>C (p.Tyr550Ser)
c.1985A>C (p.Tyr662Ser)
c.1988A>C (p.Tyr663Ser)
c.1712A>C (p.Tyr571Ser)
c.1874A>C (p.Tyr625Ser)
c.1970A>C (p.Tyr657Ser)
n.389A>C
c.1931A>C (p.Tyr644Ser)
c.1763A>C (p.Tyr588Ser)
21g.25897596A>CCA409806322APPn.2008T>G
n.438T>G
n.707T>G
c.2041T>G (p.Tyr681Asp)
c.1816T>G (p.Tyr606Asp)
c.1648T>G (p.Tyr550Asp)
c.1984T>G (p.Tyr662Asp)
c.1987T>G (p.Tyr663Asp)
c.1711T>G (p.Tyr571Asp)
c.1873T>G (p.Tyr625Asp)
c.1969T>G (p.Tyr657Asp)
n.388T>G
c.1930T>G (p.Tyr644Asp)
c.1762T>G (p.Tyr588Asp)
21g.25897596A>GCA409806319APPn.2008T>C
n.438T>C
n.707T>C
c.2041T>C (p.Tyr681His)
c.1816T>C (p.Tyr606His)
c.1648T>C (p.Tyr550His)
c.1984T>C (p.Tyr662His)
c.1987T>C (p.Tyr663His)
c.1711T>C (p.Tyr571His)
c.1873T>C (p.Tyr625His)
c.1969T>C (p.Tyr657His)
n.388T>C
c.1930T>C (p.Tyr644His)
c.1762T>C (p.Tyr588His)
21g.25897596A>TCA409806321APPn.2008T>A
n.438T>A
n.707T>A
c.2041T>A (p.Tyr681Asn)
c.1816T>A (p.Tyr606Asn)
c.1648T>A (p.Tyr550Asn)
c.1984T>A (p.Tyr662Asn)
c.1987T>A (p.Tyr663Asn)
c.1711T>A (p.Tyr571Asn)
c.1873T>A (p.Tyr625Asn)
c.1969T>A (p.Tyr657Asn)
n.388T>A
c.1930T>A (p.Tyr644Asn)
c.1762T>A (p.Tyr588Asn)
21g.25897597T>ACA511686160APPn.2007A>T
n.437A>T
n.706A>T
c.2040A>T (p.Gly680=)
c.1815A>T (p.Gly605=)
c.1647A>T (p.Gly549=)
c.1983A>T (p.Gly661=)
c.1986A>T (p.Gly662=)
c.1710A>T (p.Gly570=)
c.1872A>T (p.Gly624=)
c.1968A>T (p.Gly656=)
n.387A>T
c.1929A>T (p.Gly643=)
c.1761A>T (p.Gly587=)
21g.25897597T>CCA511686161APPn.2007A>G
n.437A>G
n.706A>G
c.2040A>G (p.Gly680=)
c.1815A>G (p.Gly605=)
c.1647A>G (p.Gly549=)
c.1983A>G (p.Gly661=)
c.1986A>G (p.Gly662=)
c.1710A>G (p.Gly570=)
c.1872A>G (p.Gly624=)
c.1968A>G (p.Gly656=)
n.387A>G
c.1929A>G (p.Gly643=)
c.1761A>G (p.Gly587=)
 gnomAD v4
21g.25897597T>GCA511686159APPn.2007A>C
n.437A>C
n.706A>C
c.2040A>C (p.Gly680=)
c.1815A>C (p.Gly605=)
c.1647A>C (p.Gly549=)
c.1983A>C (p.Gly661=)
c.1986A>C (p.Gly662=)
c.1710A>C (p.Gly570=)
c.1872A>C (p.Gly624=)
c.1968A>C (p.Gly656=)
n.387A>C
c.1929A>C (p.Gly643=)
c.1761A>C (p.Gly587=)
21g.25897598C>ACA319103384APPn.2006G>T
n.436G>T
n.705G>T
c.2039G>T (p.Gly680Val)
c.1814G>T (p.Gly605Val)
c.1646G>T (p.Gly549Val)
c.1982G>T (p.Gly661Val)
c.1985G>T (p.Gly662Val)
c.1709G>T (p.Gly570Val)
c.1871G>T (p.Gly624Val)
c.1967G>T (p.Gly656Val)
n.386G>T
c.1928G>T (p.Gly643Val)
c.1760G>T (p.Gly587Val)
 dbSNP gnomAD v4
21g.25897598C=CA2383554912APPn.2006G=
n.436G=
n.705G=
c.2039G= (p.Gly680=)
c.1814G= (p.Gly605=)
c.1646G= (p.Gly549=)
c.1982G= (p.Gly661=)
c.1985G= (p.Gly662=)
c.1709G= (p.Gly570=)
c.1871G= (p.Gly624=)
c.1967G= (p.Gly656=)
n.386G=
c.1928G= (p.Gly643=)
c.1760G= (p.Gly587=)
21g.25897598C>GCA319103385APPn.2006G>C
n.436G>C
n.705G>C
c.2039G>C (p.Gly680Ala)
c.1814G>C (p.Gly605Ala)
c.1646G>C (p.Gly549Ala)
c.1982G>C (p.Gly661Ala)
c.1985G>C (p.Gly662Ala)
c.1709G>C (p.Gly570Ala)
c.1871G>C (p.Gly624Ala)
c.1967G>C (p.Gly656Ala)
n.386G>C
c.1928G>C (p.Gly643Ala)
c.1760G>C (p.Gly587Ala)
 dbSNP gnomAD v4
21g.25897598C>TCA9987090APPn.2006G>A
n.436G>A
n.705G>A
c.2039G>A (p.Gly680Glu)
c.1814G>A (p.Gly605Glu)
c.1646G>A (p.Gly549Glu)
c.1982G>A (p.Gly661Glu)
c.1985G>A (p.Gly662Glu)
c.1709G>A (p.Gly570Glu)
c.1871G>A (p.Gly624Glu)
c.1967G>A (p.Gly656Glu)
n.386G>A
c.1928G>A (p.Gly643Glu)
c.1760G>A (p.Gly587Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
21g.25897599C>ACA409806329APPn.2005G>T
n.435G>T
n.704G>T
c.2038G>T (p.Gly680Ter)
c.1813G>T (p.Gly605Ter)
c.1645G>T (p.Gly549Ter)
c.1981G>T (p.Gly661Ter)
c.1984G>T (p.Gly662Ter)
c.1708G>T (p.Gly570Ter)
c.1870G>T (p.Gly624Ter)
c.1966G>T (p.Gly656Ter)
n.385G>T
c.1927G>T (p.Gly643Ter)
c.1759G>T (p.Gly587Ter)
21g.25897599C>GCA409806331APPn.2005G>C
n.435G>C
n.704G>C
c.2038G>C (p.Gly680Arg)
c.1813G>C (p.Gly605Arg)
c.1645G>C (p.Gly549Arg)
c.1981G>C (p.Gly661Arg)
c.1984G>C (p.Gly662Arg)
c.1708G>C (p.Gly570Arg)
c.1870G>C (p.Gly624Arg)
c.1966G>C (p.Gly656Arg)
n.385G>C
c.1927G>C (p.Gly643Arg)
c.1759G>C (p.Gly587Arg)
21g.25897599C>TCA409806332APPn.2005G>A
n.435G>A
n.704G>A
c.2038G>A (p.Gly680Arg)
c.1813G>A (p.Gly605Arg)
c.1645G>A (p.Gly549Arg)
c.1981G>A (p.Gly661Arg)
c.1984G>A (p.Gly662Arg)
c.1708G>A (p.Gly570Arg)
c.1870G>A (p.Gly624Arg)
c.1966G>A (p.Gly656Arg)
n.385G>A
c.1927G>A (p.Gly643Arg)
c.1759G>A (p.Gly587Arg)
21g.25897600T>ACA511686165APPn.2004A>T
n.434A>T
n.703A>T
c.2037A>T (p.Ser679=)
c.1812A>T (p.Ser604=)
c.1644A>T (p.Ser548=)
c.1980A>T (p.Ser660=)
c.1983A>T (p.Ser661=)
c.1707A>T (p.Ser569=)
c.1869A>T (p.Ser623=)
c.1965A>T (p.Ser655=)
n.384A>T
c.1926A>T (p.Ser642=)
c.1758A>T (p.Ser586=)
 COSMIC
21g.25897600T>CCA511686166APPn.2004A>G
n.434A>G
n.703A>G
c.2037A>G (p.Ser679=)
c.1812A>G (p.Ser604=)
c.1644A>G (p.Ser548=)
c.1980A>G (p.Ser660=)
c.1983A>G (p.Ser661=)
c.1707A>G (p.Ser569=)
c.1869A>G (p.Ser623=)
c.1965A>G (p.Ser655=)
n.384A>G
c.1926A>G (p.Ser642=)
c.1758A>G (p.Ser586=)
 gnomAD v4
21g.25897600T>GCA511686167APPn.2004A>C
n.434A>C
n.703A>C
c.2037A>C (p.Ser679=)
c.1812A>C (p.Ser604=)
c.1644A>C (p.Ser548=)
c.1980A>C (p.Ser660=)
c.1983A>C (p.Ser661=)
c.1707A>C (p.Ser569=)
c.1869A>C (p.Ser623=)
c.1965A>C (p.Ser655=)
n.384A>C
c.1926A>C (p.Ser642=)
c.1758A>C (p.Ser586=)
21g.25897601G>ACA409806335APPn.2003C>T
n.433C>T
n.702C>T
c.2036C>T (p.Ser679Leu)
c.1811C>T (p.Ser604Leu)
c.1643C>T (p.Ser548Leu)
c.1979C>T (p.Ser660Leu)
c.1982C>T (p.Ser661Leu)
c.1706C>T (p.Ser569Leu)
c.1868C>T (p.Ser623Leu)
c.1964C>T (p.Ser655Leu)
n.383C>T
c.1925C>T (p.Ser642Leu)
c.1757C>T (p.Ser586Leu)
21g.25897601G>CCA409806336APPn.2003C>G
n.433C>G
n.702C>G
c.2036C>G (p.Ser679Ter)
c.1811C>G (p.Ser604Ter)
c.1643C>G (p.Ser548Ter)
c.1979C>G (p.Ser660Ter)
c.1982C>G (p.Ser661Ter)
c.1706C>G (p.Ser569Ter)
c.1868C>G (p.Ser623Ter)
c.1964C>G (p.Ser655Ter)
n.383C>G
c.1925C>G (p.Ser642Ter)
c.1757C>G (p.Ser586Ter)
21g.25897601G>TCA409806338APPn.2003C>A
n.433C>A
n.702C>A
c.2036C>A (p.Ser679Ter)
c.1811C>A (p.Ser604Ter)
c.1643C>A (p.Ser548Ter)
c.1979C>A (p.Ser660Ter)
c.1982C>A (p.Ser661Ter)
c.1706C>A (p.Ser569Ter)
c.1868C>A (p.Ser623Ter)
c.1964C>A (p.Ser655Ter)
n.383C>A
c.1925C>A (p.Ser642Ter)
c.1757C>A (p.Ser586Ter)
 COSMIC
21g.25897602A>CCA409806340APPn.2002T>G
n.432T>G
n.701T>G
c.2035T>G (p.Ser679Ala)
c.1810T>G (p.Ser604Ala)
c.1642T>G (p.Ser548Ala)
c.1978T>G (p.Ser660Ala)
c.1981T>G (p.Ser661Ala)
c.1705T>G (p.Ser569Ala)
c.1867T>G (p.Ser623Ala)
c.1963T>G (p.Ser655Ala)
n.382T>G
c.1924T>G (p.Ser642Ala)
c.1756T>G (p.Ser586Ala)
21g.25897602A>GCA409806342APPn.2002T>C
n.432T>C
n.701T>C
c.2035T>C (p.Ser679Pro)
c.1810T>C (p.Ser604Pro)
c.1642T>C (p.Ser548Pro)
c.1978T>C (p.Ser660Pro)
c.1981T>C (p.Ser661Pro)
c.1705T>C (p.Ser569Pro)
c.1867T>C (p.Ser623Pro)
c.1963T>C (p.Ser655Pro)
n.382T>C
c.1924T>C (p.Ser642Pro)
c.1756T>C (p.Ser586Pro)
21g.25897602A>TCA409806344APPn.2002T>A
n.432T>A
n.701T>A
c.2035T>A (p.Ser679Thr)
c.1810T>A (p.Ser604Thr)
c.1642T>A (p.Ser548Thr)
c.1978T>A (p.Ser660Thr)
c.1981T>A (p.Ser661Thr)
c.1705T>A (p.Ser569Thr)
c.1867T>A (p.Ser623Thr)
c.1963T>A (p.Ser655Thr)
n.382T>A
c.1924T>A (p.Ser642Thr)
c.1756T>A (p.Ser586Thr)
21g.25897603G>ACA511686168APPn.2001C>T
n.431C>T
n.700C>T
c.2034C>T (p.Asp678=)
c.1809C>T (p.Asp603=)
c.1641C>T (p.Asp547=)
c.1977C>T (p.Asp659=)
c.1980C>T (p.Asp660=)
c.1704C>T (p.Asp568=)
c.1866C>T (p.Asp622=)
c.1962C>T (p.Asp654=)
n.381C>T
c.1923C>T (p.Asp641=)
c.1755C>T (p.Asp585=)
21g.25897603G>CCA409806347APPn.2001C>G
n.431C>G
n.700C>G
c.2034C>G (p.Asp678Glu)
c.1809C>G (p.Asp603Glu)
c.1641C>G (p.Asp547Glu)
c.1977C>G (p.Asp659Glu)
c.1980C>G (p.Asp660Glu)
c.1704C>G (p.Asp568Glu)
c.1866C>G (p.Asp622Glu)
c.1962C>G (p.Asp654Glu)
n.381C>G
c.1923C>G (p.Asp641Glu)
c.1755C>G (p.Asp585Glu)
 dbSNP
21g.25897603G=CA2383554913APPn.2001C=
n.431C=
n.700C=
c.2034C= (p.Asp678=)
c.1809C= (p.Asp603=)
c.1641C= (p.Asp547=)
c.1977C= (p.Asp659=)
c.1980C= (p.Asp660=)
c.1704C= (p.Asp568=)
c.1866C= (p.Asp622=)
c.1962C= (p.Asp654=)
n.381C=
c.1923C= (p.Asp641=)
c.1755C= (p.Asp585=)
21g.25897603G>TCA409806345APPn.2001C>A
n.431C>A
n.700C>A
c.2034C>A (p.Asp678Glu)
c.1809C>A (p.Asp603Glu)
c.1641C>A (p.Asp547Glu)
c.1977C>A (p.Asp659Glu)
c.1980C>A (p.Asp660Glu)
c.1704C>A (p.Asp568Glu)
c.1866C>A (p.Asp622Glu)
c.1962C>A (p.Asp654Glu)
n.381C>A
c.1923C>A (p.Asp641Glu)
c.1755C>A (p.Asp585Glu)
21g.25897604T>ACA409806349APPn.2000A>T
n.430A>T
n.699A>T
c.2033A>T (p.Asp678Val)
c.1808A>T (p.Asp603Val)
c.1640A>T (p.Asp547Val)
c.1976A>T (p.Asp659Val)
c.1979A>T (p.Asp660Val)
c.1703A>T (p.Asp568Val)
c.1865A>T (p.Asp622Val)
c.1961A>T (p.Asp654Val)
n.380A>T
c.1922A>T (p.Asp641Val)
c.1754A>T (p.Asp585Val)
21g.25897604T>CCA409806351APPn.2000A>G
n.430A>G
n.699A>G
c.2033A>G (p.Asp678Gly)
c.1808A>G (p.Asp603Gly)
c.1640A>G (p.Asp547Gly)
c.1976A>G (p.Asp659Gly)
c.1979A>G (p.Asp660Gly)
c.1703A>G (p.Asp568Gly)
c.1865A>G (p.Asp622Gly)
c.1961A>G (p.Asp654Gly)
n.380A>G
c.1922A>G (p.Asp641Gly)
c.1754A>G (p.Asp585Gly)
21g.25897604T>GCA409806353APPn.2000A>C
n.430A>C
n.699A>C
c.2033A>C (p.Asp678Ala)
c.1808A>C (p.Asp603Ala)
c.1640A>C (p.Asp547Ala)
c.1976A>C (p.Asp659Ala)
c.1979A>C (p.Asp660Ala)
c.1703A>C (p.Asp568Ala)
c.1865A>C (p.Asp622Ala)
c.1961A>C (p.Asp654Ala)
n.380A>C
c.1922A>C (p.Asp641Ala)
c.1754A>C (p.Asp585Ala)
21g.25897605C>ACA409806355APPn.1999G>T
n.429G>T
n.698G>T
c.2032G>T (p.Asp678Tyr)
c.1807G>T (p.Asp603Tyr)
c.1639G>T (p.Asp547Tyr)
c.1975G>T (p.Asp659Tyr)
c.1978G>T (p.Asp660Tyr)
c.1702G>T (p.Asp568Tyr)
c.1864G>T (p.Asp622Tyr)
c.1960G>T (p.Asp654Tyr)
n.379G>T
c.1921G>T (p.Asp641Tyr)
c.1753G>T (p.Asp585Tyr)
21g.25897605C=CA2383554914APPn.1999G=
n.429G=
n.698G=
c.2032G= (p.Asp678=)
c.1807G= (p.Asp603=)
c.1639G= (p.Asp547=)
c.1975G= (p.Asp659=)
c.1978G= (p.Asp660=)
c.1702G= (p.Asp568=)
c.1864G= (p.Asp622=)
c.1960G= (p.Asp654=)
n.379G=
c.1921G= (p.Asp641=)
c.1753G= (p.Asp585=)
21g.25897605C>GCA409806357APPn.1999G>C
n.429G>C
n.698G>C
c.2032G>C (p.Asp678His)
c.1807G>C (p.Asp603His)
c.1639G>C (p.Asp547His)
c.1975G>C (p.Asp659His)
c.1978G>C (p.Asp660His)
c.1702G>C (p.Asp568His)
c.1864G>C (p.Asp622His)
c.1960G>C (p.Asp654His)
n.379G>C
c.1921G>C (p.Asp641His)
c.1753G>C (p.Asp585His)
 ClinVar dbSNP

Number of alleles fetched