Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.25897576T>ACA409806220APPn.2028A>T
n.458A>T
n.727A>T
c.2061A>T (p.Lys687Asn)
c.1836A>T (p.Lys612Asn)
c.1668A>T (p.Lys556Asn)
c.2004A>T (p.Lys668Asn)
c.2007A>T (p.Lys669Asn)
c.1731A>T (p.Lys577Asn)
c.1893A>T (p.Lys631Asn)
c.1989A>T (p.Lys663Asn)
n.408A>T
c.1950A>T (p.Lys650Asn)
c.1782A>T (p.Lys594Asn)
21g.25897576T>CCA319103367APPn.2028A>G
n.458A>G
n.727A>G
c.2061A>G (p.Lys687=)
c.1836A>G (p.Lys612=)
c.1668A>G (p.Lys556=)
c.2004A>G (p.Lys668=)
c.2007A>G (p.Lys669=)
c.1731A>G (p.Lys577=)
c.1893A>G (p.Lys631=)
c.1989A>G (p.Lys663=)
n.408A>G
c.1950A>G (p.Lys650=)
c.1782A>G (p.Lys594=)
dbSNP gnomAD v4
21g.25897576T>GCA409806222APPn.2028A>C
n.458A>C
n.727A>C
c.2061A>C (p.Lys687Asn)
c.1836A>C (p.Lys612Asn)
c.1668A>C (p.Lys556Asn)
c.2004A>C (p.Lys668Asn)
c.2007A>C (p.Lys669Asn)
c.1731A>C (p.Lys577Asn)
c.1893A>C (p.Lys631Asn)
c.1989A>C (p.Lys663Asn)
n.408A>C
c.1950A>C (p.Lys650Asn)
c.1782A>C (p.Lys594Asn)
ClinVar
21g.25897576T=CA2383554901APPn.2028A=
n.458A=
n.727A=
c.2061A= (p.Lys687=)
c.1836A= (p.Lys612=)
c.1668A= (p.Lys556=)
c.2004A= (p.Lys668=)
c.2007A= (p.Lys669=)
c.1731A= (p.Lys577=)
c.1893A= (p.Lys631=)
c.1989A= (p.Lys663=)
n.408A=
c.1950A= (p.Lys650=)
c.1782A= (p.Lys594=)
21g.25897577T>ACA409806228APPn.2027A>T
n.457A>T
n.726A>T
c.2060A>T (p.Lys687Ile)
c.1835A>T (p.Lys612Ile)
c.1667A>T (p.Lys556Ile)
c.2003A>T (p.Lys668Ile)
c.2006A>T (p.Lys669Ile)
c.1730A>T (p.Lys577Ile)
c.1892A>T (p.Lys631Ile)
c.1988A>T (p.Lys663Ile)
n.407A>T
c.1949A>T (p.Lys650Ile)
c.1781A>T (p.Lys594Ile)
21g.25897577T>CCA409806227APPn.2027A>G
n.457A>G
n.726A>G
c.2060A>G (p.Lys687Arg)
c.1835A>G (p.Lys612Arg)
c.1667A>G (p.Lys556Arg)
c.2003A>G (p.Lys668Arg)
c.2006A>G (p.Lys669Arg)
c.1730A>G (p.Lys577Arg)
c.1892A>G (p.Lys631Arg)
c.1988A>G (p.Lys663Arg)
n.407A>G
c.1949A>G (p.Lys650Arg)
c.1781A>G (p.Lys594Arg)
dbSNP gnomAD v3 gnomAD v4
21g.25897577T>GCA409806225APPn.2027A>C
n.457A>C
n.726A>C
c.2060A>C (p.Lys687Thr)
c.1835A>C (p.Lys612Thr)
c.1667A>C (p.Lys556Thr)
c.2003A>C (p.Lys668Thr)
c.2006A>C (p.Lys669Thr)
c.1730A>C (p.Lys577Thr)
c.1892A>C (p.Lys631Thr)
c.1988A>C (p.Lys663Thr)
n.407A>C
c.1949A>C (p.Lys650Thr)
c.1781A>C (p.Lys594Thr)
21g.25897577T=CA2383554902APPn.2027A=
n.457A=
n.726A=
c.2060A= (p.Lys687=)
c.1835A= (p.Lys612=)
c.1667A= (p.Lys556=)
c.2003A= (p.Lys668=)
c.2006A= (p.Lys669=)
c.1730A= (p.Lys577=)
c.1892A= (p.Lys631=)
c.1988A= (p.Lys663=)
n.407A=
c.1949A= (p.Lys650=)
c.1781A= (p.Lys594=)
21g.25897578T>ACA409806231APPn.2026A>T
n.456A>T
n.725A>T
c.2059A>T (p.Lys687Ter)
c.1834A>T (p.Lys612Ter)
c.1666A>T (p.Lys556Ter)
c.2002A>T (p.Lys668Ter)
c.2005A>T (p.Lys669Ter)
c.1729A>T (p.Lys577Ter)
c.1891A>T (p.Lys631Ter)
c.1987A>T (p.Lys663Ter)
n.406A>T
c.1948A>T (p.Lys650Ter)
c.1780A>T (p.Lys594Ter)
21g.25897578T>CCA409806233APPn.2026A>G
n.456A>G
n.725A>G
c.2059A>G (p.Lys687Glu)
c.1834A>G (p.Lys612Glu)
c.1666A>G (p.Lys556Glu)
c.2002A>G (p.Lys668Glu)
c.2005A>G (p.Lys669Glu)
c.1729A>G (p.Lys577Glu)
c.1891A>G (p.Lys631Glu)
c.1987A>G (p.Lys663Glu)
n.406A>G
c.1948A>G (p.Lys650Glu)
c.1780A>G (p.Lys594Glu)
21g.25897578T>GCA409806235APPn.2026A>C
n.456A>C
n.725A>C
c.2059A>C (p.Lys687Gln)
c.1834A>C (p.Lys612Gln)
c.1666A>C (p.Lys556Gln)
c.2002A>C (p.Lys668Gln)
c.2005A>C (p.Lys669Gln)
c.1729A>C (p.Lys577Gln)
c.1891A>C (p.Lys631Gln)
c.1987A>C (p.Lys663Gln)
n.406A>C
c.1948A>C (p.Lys650Gln)
c.1780A>C (p.Lys594Gln)
21g.25897579T>ACA409806237APPn.2025A>T
n.455A>T
n.724A>T
c.2058A>T (p.Gln686His)
c.1833A>T (p.Gln611His)
c.1665A>T (p.Gln555His)
c.2001A>T (p.Gln667His)
c.2004A>T (p.Gln668His)
c.1728A>T (p.Gln576His)
c.1890A>T (p.Gln630His)
c.1986A>T (p.Gln662His)
n.405A>T
c.1947A>T (p.Gln649His)
c.1779A>T (p.Gln593His)
COSMIC
21g.25897579T>CCA511686138APPn.2025A>G
n.455A>G
n.724A>G
c.2058A>G (p.Gln686=)
c.1833A>G (p.Gln611=)
c.1665A>G (p.Gln555=)
c.2001A>G (p.Gln667=)
c.2004A>G (p.Gln668=)
c.1728A>G (p.Gln576=)
c.1890A>G (p.Gln630=)
c.1986A>G (p.Gln662=)
n.405A>G
c.1947A>G (p.Gln649=)
c.1779A>G (p.Gln593=)
dbSNP gnomAD v3 gnomAD v4
21g.25897579T>GCA409806239APPn.2025A>C
n.455A>C
n.724A>C
c.2058A>C (p.Gln686His)
c.1833A>C (p.Gln611His)
c.1665A>C (p.Gln555His)
c.2001A>C (p.Gln667His)
c.2004A>C (p.Gln668His)
c.1728A>C (p.Gln576His)
c.1890A>C (p.Gln630His)
c.1986A>C (p.Gln662His)
n.405A>C
c.1947A>C (p.Gln649His)
c.1779A>C (p.Gln593His)
21g.25897579T=CA2383554904APPn.2025A=
n.455A=
n.724A=
c.2058A= (p.Gln686=)
c.1833A= (p.Gln611=)
c.1665A= (p.Gln555=)
c.2001A= (p.Gln667=)
c.2004A= (p.Gln668=)
c.1728A= (p.Gln576=)
c.1890A= (p.Gln630=)
c.1986A= (p.Gln662=)
n.405A=
c.1947A= (p.Gln649=)
c.1779A= (p.Gln593=)
21g.25897579_25897582delinsTTGACA2383554903APPn.2022_2025delinsTCAA
n.452_455delinsTCAA
n.721_724delinsTCAA
c.2055_2058delinsTCAA (p.His685=)
c.1830_1833delinsTCAA (p.His610=)
c.1662_1665delinsTCAA (p.His554=)
c.1998_2001delinsTCAA (p.His666=)
c.2001_2004delinsTCAA (p.His667=)
c.1725_1728delinsTCAA (p.His575=)
c.1887_1890delinsTCAA (p.His629=)
c.1983_1986delinsTCAA (p.His661=)
n.402_405delinsTCAA
c.1944_1947delinsTCAA (p.His648=)
c.1776_1779delinsTCAA (p.His592=)
21g.25897580T>ACA409806241APPn.2024A>T
n.454A>T
n.723A>T
c.2057A>T (p.Gln686Leu)
c.1832A>T (p.Gln611Leu)
c.1664A>T (p.Gln555Leu)
c.2000A>T (p.Gln667Leu)
c.2003A>T (p.Gln668Leu)
c.1727A>T (p.Gln576Leu)
c.1889A>T (p.Gln630Leu)
c.1985A>T (p.Gln662Leu)
n.404A>T
c.1946A>T (p.Gln649Leu)
c.1778A>T (p.Gln593Leu)
21g.25897580T>CCA409806242APPn.2024A>G
n.454A>G
n.723A>G
c.2057A>G (p.Gln686Arg)
c.1832A>G (p.Gln611Arg)
c.1664A>G (p.Gln555Arg)
c.2000A>G (p.Gln667Arg)
c.2003A>G (p.Gln668Arg)
c.1727A>G (p.Gln576Arg)
c.1889A>G (p.Gln630Arg)
c.1985A>G (p.Gln662Arg)
n.404A>G
c.1946A>G (p.Gln649Arg)
c.1778A>G (p.Gln593Arg)
21g.25897580T>GCA409806244APPn.2024A>C
n.454A>C
n.723A>C
c.2057A>C (p.Gln686Pro)
c.1832A>C (p.Gln611Pro)
c.1664A>C (p.Gln555Pro)
c.2000A>C (p.Gln667Pro)
c.2003A>C (p.Gln668Pro)
c.1727A>C (p.Gln576Pro)
c.1889A>C (p.Gln630Pro)
c.1985A>C (p.Gln662Pro)
n.404A>C
c.1946A>C (p.Gln649Pro)
c.1778A>C (p.Gln593Pro)
COSMIC
21g.25897586_25897588delCA511686140APPn.2022_2024del
n.452_454del
n.721_723del
c.2055_2057del (p.His685del)
c.1830_1832del (p.His610del)
c.1662_1664del (p.His554del)
c.1998_2000del (p.His666del)
c.2001_2003del (p.His667del)
c.1725_1727del (p.His575del)
c.1887_1889del (p.His629del)
c.1983_1985del (p.His661del)
n.402_404del
c.1944_1946del (p.His648del)
c.1776_1778del (p.His592del)
dbSNP gnomAD v2
21g.25897581G>ACA409806246APPn.2023C>T
n.453C>T
n.722C>T
c.2056C>T (p.Gln686Ter)
c.1831C>T (p.Gln611Ter)
c.1663C>T (p.Gln555Ter)
c.1999C>T (p.Gln667Ter)
c.2002C>T (p.Gln668Ter)
c.1726C>T (p.Gln576Ter)
c.1888C>T (p.Gln630Ter)
c.1984C>T (p.Gln662Ter)
n.403C>T
c.1945C>T (p.Gln649Ter)
c.1777C>T (p.Gln593Ter)
21g.25897581G>CCA409806248APPn.2023C>G
n.453C>G
n.722C>G
c.2056C>G (p.Gln686Glu)
c.1831C>G (p.Gln611Glu)
c.1663C>G (p.Gln555Glu)
c.1999C>G (p.Gln667Glu)
c.2002C>G (p.Gln668Glu)
c.1726C>G (p.Gln576Glu)
c.1888C>G (p.Gln630Glu)
c.1984C>G (p.Gln662Glu)
n.403C>G
c.1945C>G (p.Gln649Glu)
c.1777C>G (p.Gln593Glu)
dbSNP gnomAD v4
21g.25897581G=CA2383554905APPn.2023C=
n.453C=
n.722C=
c.2056C= (p.Gln686=)
c.1831C= (p.Gln611=)
c.1663C= (p.Gln555=)
c.1999C= (p.Gln667=)
c.2002C= (p.Gln668=)
c.1726C= (p.Gln576=)
c.1888C= (p.Gln630=)
c.1984C= (p.Gln662=)
n.403C=
c.1945C= (p.Gln649=)
c.1777C= (p.Gln593=)
21g.25897581G>TCA409806250APPn.2023C>A
n.453C>A
n.722C>A
c.2056C>A (p.Gln686Lys)
c.1831C>A (p.Gln611Lys)
c.1663C>A (p.Gln555Lys)
c.1999C>A (p.Gln667Lys)
c.2002C>A (p.Gln668Lys)
c.1726C>A (p.Gln576Lys)
c.1888C>A (p.Gln630Lys)
c.1984C>A (p.Gln662Lys)
n.403C>A
c.1945C>A (p.Gln649Lys)
c.1777C>A (p.Gln593Lys)
COSMIC
21g.25897582A>CCA409806252APPn.2022T>G
n.452T>G
n.721T>G
c.2055T>G (p.His685Gln)
c.1830T>G (p.His610Gln)
c.1662T>G (p.His554Gln)
c.1998T>G (p.His666Gln)
c.2001T>G (p.His667Gln)
c.1725T>G (p.His575Gln)
c.1887T>G (p.His629Gln)
c.1983T>G (p.His661Gln)
n.402T>G
c.1944T>G (p.His648Gln)
c.1776T>G (p.His592Gln)
21g.25897582A>GCA511686143APPn.2022T>C
n.452T>C
n.721T>C
c.2055T>C (p.His685=)
c.1830T>C (p.His610=)
c.1662T>C (p.His554=)
c.1998T>C (p.His666=)
c.2001T>C (p.His667=)
c.1725T>C (p.His575=)
c.1887T>C (p.His629=)
c.1983T>C (p.His661=)
n.402T>C
c.1944T>C (p.His648=)
c.1776T>C (p.His592=)
21g.25897582A>TCA409806253APPn.2022T>A
n.452T>A
n.721T>A
c.2055T>A (p.His685Gln)
c.1830T>A (p.His610Gln)
c.1662T>A (p.His554Gln)
c.1998T>A (p.His666Gln)
c.2001T>A (p.His667Gln)
c.1725T>A (p.His575Gln)
c.1887T>A (p.His629Gln)
c.1983T>A (p.His661Gln)
n.402T>A
c.1944T>A (p.His648Gln)
c.1776T>A (p.His592Gln)
21g.25897583T>ACA409806258APPn.2021A>T
n.451A>T
n.720A>T
c.2054A>T (p.His685Leu)
c.1829A>T (p.His610Leu)
c.1661A>T (p.His554Leu)
c.1997A>T (p.His666Leu)
c.2000A>T (p.His667Leu)
c.1724A>T (p.His575Leu)
c.1886A>T (p.His629Leu)
c.1982A>T (p.His661Leu)
n.401A>T
c.1943A>T (p.His648Leu)
c.1775A>T (p.His592Leu)
21g.25897583T>CCA9987087APPn.2021A>G
n.451A>G
n.720A>G
c.2054A>G (p.His685Arg)
c.1829A>G (p.His610Arg)
c.1661A>G (p.His554Arg)
c.1997A>G (p.His666Arg)
c.2000A>G (p.His667Arg)
c.1724A>G (p.His575Arg)
c.1886A>G (p.His629Arg)
c.1982A>G (p.His661Arg)
n.401A>G
c.1943A>G (p.His648Arg)
c.1775A>G (p.His592Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
21g.25897583T>GCA409806256APPn.2021A>C
n.451A>C
n.720A>C
c.2054A>C (p.His685Pro)
c.1829A>C (p.His610Pro)
c.1661A>C (p.His554Pro)
c.1997A>C (p.His666Pro)
c.2000A>C (p.His667Pro)
c.1724A>C (p.His575Pro)
c.1886A>C (p.His629Pro)
c.1982A>C (p.His661Pro)
n.401A>C
c.1943A>C (p.His648Pro)
c.1775A>C (p.His592Pro)
21g.25897583T=CA2383554906APPn.2021A=
n.451A=
n.720A=
c.2054A= (p.His685=)
c.1829A= (p.His610=)
c.1661A= (p.His554=)
c.1997A= (p.His666=)
c.2000A= (p.His667=)
c.1724A= (p.His575=)
c.1886A= (p.His629=)
c.1982A= (p.His661=)
n.401A=
c.1943A= (p.His648=)
c.1775A= (p.His592=)
21g.25897584G>ACA409806261APPn.2020C>T
n.450C>T
n.719C>T
c.2053C>T (p.His685Tyr)
c.1828C>T (p.His610Tyr)
c.1660C>T (p.His554Tyr)
c.1996C>T (p.His666Tyr)
c.1999C>T (p.His667Tyr)
c.1723C>T (p.His575Tyr)
c.1885C>T (p.His629Tyr)
c.1981C>T (p.His661Tyr)
n.400C>T
c.1942C>T (p.His648Tyr)
c.1774C>T (p.His592Tyr)
21g.25897584G>CCA409806262APPn.2020C>G
n.450C>G
n.719C>G
c.2053C>G (p.His685Asp)
c.1828C>G (p.His610Asp)
c.1660C>G (p.His554Asp)
c.1996C>G (p.His666Asp)
c.1999C>G (p.His667Asp)
c.1723C>G (p.His575Asp)
c.1885C>G (p.His629Asp)
c.1981C>G (p.His661Asp)
n.400C>G
c.1942C>G (p.His648Asp)
c.1774C>G (p.His592Asp)
21g.25897584G>TCA409806264APPn.2020C>A
n.450C>A
n.719C>A
c.2053C>A (p.His685Asn)
c.1828C>A (p.His610Asn)
c.1660C>A (p.His554Asn)
c.1996C>A (p.His666Asn)
c.1999C>A (p.His667Asn)
c.1723C>A (p.His575Asn)
c.1885C>A (p.His629Asn)
c.1981C>A (p.His661Asn)
n.400C>A
c.1942C>A (p.His648Asn)
c.1774C>A (p.His592Asn)
21g.25897585A>CCA409806266APPn.2019T>G
n.449T>G
n.718T>G
c.2052T>G (p.His684Gln)
c.1827T>G (p.His609Gln)
c.1659T>G (p.His553Gln)
c.1995T>G (p.His665Gln)
c.1998T>G (p.His666Gln)
c.1722T>G (p.His574Gln)
c.1884T>G (p.His628Gln)
c.1980T>G (p.His660Gln)
n.399T>G
c.1941T>G (p.His647Gln)
c.1773T>G (p.His591Gln)
21g.25897585A>GCA511686146APPn.2019T>C
n.449T>C
n.718T>C
c.2052T>C (p.His684=)
c.1827T>C (p.His609=)
c.1659T>C (p.His553=)
c.1995T>C (p.His665=)
c.1998T>C (p.His666=)
c.1722T>C (p.His574=)
c.1884T>C (p.His628=)
c.1980T>C (p.His660=)
n.399T>C
c.1941T>C (p.His647=)
c.1773T>C (p.His591=)
21g.25897585A>TCA409806268APPn.2019T>A
n.449T>A
n.718T>A
c.2052T>A (p.His684Gln)
c.1827T>A (p.His609Gln)
c.1659T>A (p.His553Gln)
c.1995T>A (p.His665Gln)
c.1998T>A (p.His666Gln)
c.1722T>A (p.His574Gln)
c.1884T>A (p.His628Gln)
c.1980T>A (p.His660Gln)
n.399T>A
c.1941T>A (p.His647Gln)
c.1773T>A (p.His591Gln)
COSMIC
21g.25897586T>ACA409806270APPn.2018A>T
n.448A>T
n.717A>T
c.2051A>T (p.His684Leu)
c.1826A>T (p.His609Leu)
c.1658A>T (p.His553Leu)
c.1994A>T (p.His665Leu)
c.1997A>T (p.His666Leu)
c.1721A>T (p.His574Leu)
c.1883A>T (p.His628Leu)
c.1979A>T (p.His660Leu)
n.398A>T
c.1940A>T (p.His647Leu)
c.1772A>T (p.His591Leu)
dbSNP
21g.25897586T>CCA409806272APPn.2018A>G
n.448A>G
n.717A>G
c.2051A>G (p.His684Arg)
c.1826A>G (p.His609Arg)
c.1658A>G (p.His553Arg)
c.1994A>G (p.His665Arg)
c.1997A>G (p.His666Arg)
c.1721A>G (p.His574Arg)
c.1883A>G (p.His628Arg)
c.1979A>G (p.His660Arg)
n.398A>G
c.1940A>G (p.His647Arg)
c.1772A>G (p.His591Arg)
gnomAD v4
21g.25897586T>GCA409806274APPn.2018A>C
n.448A>C
n.717A>C
c.2051A>C (p.His684Pro)
c.1826A>C (p.His609Pro)
c.1658A>C (p.His553Pro)
c.1994A>C (p.His665Pro)
c.1997A>C (p.His666Pro)
c.1721A>C (p.His574Pro)
c.1883A>C (p.His628Pro)
c.1979A>C (p.His660Pro)
n.398A>C
c.1940A>C (p.His647Pro)
c.1772A>C (p.His591Pro)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
21g.25897586T=CA2383554907APPn.2018A=
n.448A=
n.717A=
c.2051A= (p.His684=)
c.1826A= (p.His609=)
c.1658A= (p.His553=)
c.1994A= (p.His665=)
c.1997A= (p.His666=)
c.1721A= (p.His574=)
c.1883A= (p.His628=)
c.1979A= (p.His660=)
n.398A=
c.1940A= (p.His647=)
c.1772A= (p.His591=)
21g.25897587G>ACA409806277APPn.2017C>T
n.447C>T
n.716C>T
c.2050C>T (p.His684Tyr)
c.1825C>T (p.His609Tyr)
c.1657C>T (p.His553Tyr)
c.1993C>T (p.His665Tyr)
c.1996C>T (p.His666Tyr)
c.1720C>T (p.His574Tyr)
c.1882C>T (p.His628Tyr)
c.1978C>T (p.His660Tyr)
n.397C>T
c.1939C>T (p.His647Tyr)
c.1771C>T (p.His591Tyr)
gnomAD v4
21g.25897587G>CCA409806278APPn.2017C>G
n.447C>G
n.716C>G
c.2050C>G (p.His684Asp)
c.1825C>G (p.His609Asp)
c.1657C>G (p.His553Asp)
c.1993C>G (p.His665Asp)
c.1996C>G (p.His666Asp)
c.1720C>G (p.His574Asp)
c.1882C>G (p.His628Asp)
c.1978C>G (p.His660Asp)
n.397C>G
c.1939C>G (p.His647Asp)
c.1771C>G (p.His591Asp)
21g.25897587G>TCA409806280APPn.2017C>A
n.447C>A
n.716C>A
c.2050C>A (p.His684Asn)
c.1825C>A (p.His609Asn)
c.1657C>A (p.His553Asn)
c.1993C>A (p.His665Asn)
c.1996C>A (p.His666Asn)
c.1720C>A (p.His574Asn)
c.1882C>A (p.His628Asn)
c.1978C>A (p.His660Asn)
n.397C>A
c.1939C>A (p.His647Asn)
c.1771C>A (p.His591Asn)
21g.25897588A=CA2383554908APPn.2016T=
n.446T=
n.715T=
c.2049T= (p.Val683=)
c.1824T= (p.Val608=)
c.1656T= (p.Val552=)
c.1992T= (p.Val664=)
c.1995T= (p.Val665=)
c.1719T= (p.Val573=)
c.1881T= (p.Val627=)
c.1977T= (p.Val659=)
n.396T=
c.1938T= (p.Val646=)
c.1770T= (p.Val590=)
21g.25897588A>CCA511686150APPn.2016T>G
n.446T>G
n.715T>G
c.2049T>G (p.Val683=)
c.1824T>G (p.Val608=)
c.1656T>G (p.Val552=)
c.1992T>G (p.Val664=)
c.1995T>G (p.Val665=)
c.1719T>G (p.Val573=)
c.1881T>G (p.Val627=)
c.1977T>G (p.Val659=)
n.396T>G
c.1938T>G (p.Val646=)
c.1770T>G (p.Val590=)
21g.25897588A>GCA511686151APPn.2016T>C
n.446T>C
n.715T>C
c.2049T>C (p.Val683=)
c.1824T>C (p.Val608=)
c.1656T>C (p.Val552=)
c.1992T>C (p.Val664=)
c.1995T>C (p.Val665=)
c.1719T>C (p.Val573=)
c.1881T>C (p.Val627=)
c.1977T>C (p.Val659=)
n.396T>C
c.1938T>C (p.Val646=)
c.1770T>C (p.Val590=)
21g.25897588A>TCA9987088APPn.2016T>A
n.446T>A
n.715T>A
c.2049T>A (p.Val683=)
c.1824T>A (p.Val608=)
c.1656T>A (p.Val552=)
c.1992T>A (p.Val664=)
c.1995T>A (p.Val665=)
c.1719T>A (p.Val573=)
c.1881T>A (p.Val627=)
c.1977T>A (p.Val659=)
n.396T>A
c.1938T>A (p.Val646=)
c.1770T>A (p.Val590=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.25897589A>CCA409806285APPn.2015T>G
n.445T>G
n.714T>G
c.2048T>G (p.Val683Gly)
c.1823T>G (p.Val608Gly)
c.1655T>G (p.Val552Gly)
c.1991T>G (p.Val664Gly)
c.1994T>G (p.Val665Gly)
c.1718T>G (p.Val573Gly)
c.1880T>G (p.Val627Gly)
c.1976T>G (p.Val659Gly)
n.395T>G
c.1937T>G (p.Val646Gly)
c.1769T>G (p.Val590Gly)
21g.25897589A>GCA409806287APPn.2015T>C
n.445T>C
n.714T>C
c.2048T>C (p.Val683Ala)
c.1823T>C (p.Val608Ala)
c.1655T>C (p.Val552Ala)
c.1991T>C (p.Val664Ala)
c.1994T>C (p.Val665Ala)
c.1718T>C (p.Val573Ala)
c.1880T>C (p.Val627Ala)
c.1976T>C (p.Val659Ala)
n.395T>C
c.1937T>C (p.Val646Ala)
c.1769T>C (p.Val590Ala)

Number of alleles fetched