Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.25897649_25897655delinsGTCTTGACA2383554945APPn.1949_1955delinsTCAAGAC
n.379_385delinsTCAAGAC
n.648_654delinsTCAAGAC
c.1982_1988delinsTCAAGAC (p.Ile661=)
c.1757_1763delinsTCAAGAC (p.Ile586=)
c.1589_1595delinsTCAAGAC (p.Ile530=)
c.1925_1931delinsTCAAGAC (p.Ile642=)
c.1928_1934delinsTCAAGAC (p.Ile643=)
c.1652_1658delinsTCAAGAC (p.Ile551=)
c.1814_1820delinsTCAAGAC (p.Ile605=)
c.1910_1916delinsTCAAGAC (p.Ile637=)
n.329_335delinsTCAAGAC
c.1871_1877delinsTCAAGAC (p.Ile624=)
c.1703_1709delinsTCAAGAC (p.Ile568=)
21g.25897651_25897656delCA2383554946APPn.1949_1954del
n.379_384del
n.648_653del
c.1982_1987del (p.Ile661_Lys662del)
c.1757_1762del (p.Ile586_Lys587del)
c.1589_1594del (p.Ile530_Lys531del)
c.1925_1930del (p.Ile642_Lys643del)
c.1928_1933del (p.Ile643_Lys644del)
c.1652_1657del (p.Ile551_Lys552del)
c.1814_1819del (p.Ile605_Lys606del)
c.1910_1915del (p.Ile637_Lys638del)
n.329_334del
c.1871_1876del (p.Ile624_Lys625del)
c.1703_1708del (p.Ile568_Lys569del)
dbSNP
21g.25897652T>ACA409806550APPn.1952A>T
n.382A>T
n.651A>T
c.1985A>T (p.Lys662Met)
c.1760A>T (p.Lys587Met)
c.1592A>T (p.Lys531Met)
c.1928A>T (p.Lys643Met)
c.1931A>T (p.Lys644Met)
c.1655A>T (p.Lys552Met)
c.1817A>T (p.Lys606Met)
c.1913A>T (p.Lys638Met)
n.332A>T
c.1874A>T (p.Lys625Met)
c.1706A>T (p.Lys569Met)
21g.25897652T>CCA409806551APPn.1952A>G
n.382A>G
n.651A>G
c.1985A>G (p.Lys662Arg)
c.1760A>G (p.Lys587Arg)
c.1592A>G (p.Lys531Arg)
c.1928A>G (p.Lys643Arg)
c.1931A>G (p.Lys644Arg)
c.1655A>G (p.Lys552Arg)
c.1817A>G (p.Lys606Arg)
c.1913A>G (p.Lys638Arg)
n.332A>G
c.1874A>G (p.Lys625Arg)
c.1706A>G (p.Lys569Arg)
21g.25897652T>GCA409806552APPn.1952A>C
n.382A>C
n.651A>C
c.1985A>C (p.Lys662Thr)
c.1760A>C (p.Lys587Thr)
c.1592A>C (p.Lys531Thr)
c.1928A>C (p.Lys643Thr)
c.1931A>C (p.Lys644Thr)
c.1655A>C (p.Lys552Thr)
c.1817A>C (p.Lys606Thr)
c.1913A>C (p.Lys638Thr)
n.332A>C
c.1874A>C (p.Lys625Thr)
c.1706A>C (p.Lys569Thr)
21g.25897653T>ACA409806553APPn.1951A>T
n.381A>T
n.650A>T
c.1984A>T (p.Lys662Ter)
c.1759A>T (p.Lys587Ter)
c.1591A>T (p.Lys531Ter)
c.1927A>T (p.Lys643Ter)
c.1930A>T (p.Lys644Ter)
c.1654A>T (p.Lys552Ter)
c.1816A>T (p.Lys606Ter)
c.1912A>T (p.Lys638Ter)
n.331A>T
c.1873A>T (p.Lys625Ter)
c.1705A>T (p.Lys569Ter)
21g.25897653T>CCA409806555APPn.1951A>G
n.381A>G
n.650A>G
c.1984A>G (p.Lys662Glu)
c.1759A>G (p.Lys587Glu)
c.1591A>G (p.Lys531Glu)
c.1927A>G (p.Lys643Glu)
c.1930A>G (p.Lys644Glu)
c.1654A>G (p.Lys552Glu)
c.1816A>G (p.Lys606Glu)
c.1912A>G (p.Lys638Glu)
n.331A>G
c.1873A>G (p.Lys625Glu)
c.1705A>G (p.Lys569Glu)
21g.25897653T>GCA409806554APPn.1951A>C
n.381A>C
n.650A>C
c.1984A>C (p.Lys662Gln)
c.1759A>C (p.Lys587Gln)
c.1591A>C (p.Lys531Gln)
c.1927A>C (p.Lys643Gln)
c.1930A>C (p.Lys644Gln)
c.1654A>C (p.Lys552Gln)
c.1816A>C (p.Lys606Gln)
c.1912A>C (p.Lys638Gln)
n.331A>C
c.1873A>C (p.Lys625Gln)
c.1705A>C (p.Lys569Gln)
21g.25897654G>ACA511686342APPn.1950C>T
n.380C>T
n.649C>T
c.1983C>T (p.Ile661=)
c.1758C>T (p.Ile586=)
c.1590C>T (p.Ile530=)
c.1926C>T (p.Ile642=)
c.1929C>T (p.Ile643=)
c.1653C>T (p.Ile551=)
c.1815C>T (p.Ile605=)
c.1911C>T (p.Ile637=)
n.330C>T
c.1872C>T (p.Ile624=)
c.1704C>T (p.Ile568=)
dbSNP
21g.25897654G>CCA409806556APPn.1950C>G
n.380C>G
n.649C>G
c.1983C>G (p.Ile661Met)
c.1758C>G (p.Ile586Met)
c.1590C>G (p.Ile530Met)
c.1926C>G (p.Ile642Met)
c.1929C>G (p.Ile643Met)
c.1653C>G (p.Ile551Met)
c.1815C>G (p.Ile605Met)
c.1911C>G (p.Ile637Met)
n.330C>G
c.1872C>G (p.Ile624Met)
c.1704C>G (p.Ile568Met)
21g.25897654G=CA2383554947APPn.1950C=
n.380C=
n.649C=
c.1983C= (p.Ile661=)
c.1758C= (p.Ile586=)
c.1590C= (p.Ile530=)
c.1926C= (p.Ile642=)
c.1929C= (p.Ile643=)
c.1653C= (p.Ile551=)
c.1815C= (p.Ile605=)
c.1911C= (p.Ile637=)
n.330C=
c.1872C= (p.Ile624=)
c.1704C= (p.Ile568=)
21g.25897654G>TCA511686341APPn.1950C>A
n.380C>A
n.649C>A
c.1983C>A (p.Ile661=)
c.1758C>A (p.Ile586=)
c.1590C>A (p.Ile530=)
c.1926C>A (p.Ile642=)
c.1929C>A (p.Ile643=)
c.1653C>A (p.Ile551=)
c.1815C>A (p.Ile605=)
c.1911C>A (p.Ile637=)
n.330C>A
c.1872C>A (p.Ile624=)
c.1704C>A (p.Ile568=)
21g.25897655A=CA2383554948APPn.1949T=
n.379T=
n.648T=
c.1982T= (p.Ile661=)
c.1757T= (p.Ile586=)
c.1589T= (p.Ile530=)
c.1925T= (p.Ile642=)
c.1928T= (p.Ile643=)
c.1652T= (p.Ile551=)
c.1814T= (p.Ile605=)
c.1910T= (p.Ile637=)
n.329T=
c.1871T= (p.Ile624=)
c.1703T= (p.Ile568=)
21g.25897655A>CCA409806557APPn.1949T>G
n.379T>G
n.648T>G
c.1982T>G (p.Ile661Ser)
c.1757T>G (p.Ile586Ser)
c.1589T>G (p.Ile530Ser)
c.1925T>G (p.Ile642Ser)
c.1928T>G (p.Ile643Ser)
c.1652T>G (p.Ile551Ser)
c.1814T>G (p.Ile605Ser)
c.1910T>G (p.Ile637Ser)
n.329T>G
c.1871T>G (p.Ile624Ser)
c.1703T>G (p.Ile568Ser)
gnomAD v4
21g.25897655A>GCA9987105APPn.1949T>C
n.379T>C
n.648T>C
c.1982T>C (p.Ile661Thr)
c.1757T>C (p.Ile586Thr)
c.1589T>C (p.Ile530Thr)
c.1925T>C (p.Ile642Thr)
c.1928T>C (p.Ile643Thr)
c.1652T>C (p.Ile551Thr)
c.1814T>C (p.Ile605Thr)
c.1910T>C (p.Ile637Thr)
n.329T>C
c.1871T>C (p.Ile624Thr)
c.1703T>C (p.Ile568Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.25897655A>TCA409806558APPn.1949T>A
n.379T>A
n.648T>A
c.1982T>A (p.Ile661Asn)
c.1757T>A (p.Ile586Asn)
c.1589T>A (p.Ile530Asn)
c.1925T>A (p.Ile642Asn)
c.1928T>A (p.Ile643Asn)
c.1652T>A (p.Ile551Asn)
c.1814T>A (p.Ile605Asn)
c.1910T>A (p.Ile637Asn)
n.329T>A
c.1871T>A (p.Ile624Asn)
c.1703T>A (p.Ile568Asn)
21g.25897656T>ACA409806559APPn.1948A>T
n.378A>T
n.647A>T
c.1981A>T (p.Ile661Phe)
c.1756A>T (p.Ile586Phe)
c.1588A>T (p.Ile530Phe)
c.1924A>T (p.Ile642Phe)
c.1927A>T (p.Ile643Phe)
c.1651A>T (p.Ile551Phe)
c.1813A>T (p.Ile605Phe)
c.1909A>T (p.Ile637Phe)
n.328A>T
c.1870A>T (p.Ile624Phe)
c.1702A>T (p.Ile568Phe)
21g.25897656T>CCA319103568APPn.1948A>G
n.378A>G
n.647A>G
c.1981A>G (p.Ile661Val)
c.1756A>G (p.Ile586Val)
c.1588A>G (p.Ile530Val)
c.1924A>G (p.Ile642Val)
c.1927A>G (p.Ile643Val)
c.1651A>G (p.Ile551Val)
c.1813A>G (p.Ile605Val)
c.1909A>G (p.Ile637Val)
n.328A>G
c.1870A>G (p.Ile624Val)
c.1702A>G (p.Ile568Val)
dbSNP gnomAD v2 gnomAD v4
21g.25897656T>GCA409806560APPn.1948A>C
n.378A>C
n.647A>C
c.1981A>C (p.Ile661Leu)
c.1756A>C (p.Ile586Leu)
c.1588A>C (p.Ile530Leu)
c.1924A>C (p.Ile642Leu)
c.1927A>C (p.Ile643Leu)
c.1651A>C (p.Ile551Leu)
c.1813A>C (p.Ile605Leu)
c.1909A>C (p.Ile637Leu)
n.328A>C
c.1870A>C (p.Ile624Leu)
c.1702A>C (p.Ile568Leu)
21g.25897656T=CA2383554949APPn.1948A=
n.378A=
n.647A=
c.1981A= (p.Ile661=)
c.1756A= (p.Ile586=)
c.1588A= (p.Ile530=)
c.1924A= (p.Ile642=)
c.1927A= (p.Ile643=)
c.1651A= (p.Ile551=)
c.1813A= (p.Ile605=)
c.1909A= (p.Ile637=)
n.328A=
c.1870A= (p.Ile624=)
c.1702A= (p.Ile568=)
21g.25897657A=CA2383554950APPn.1947T=
n.377T=
n.646T=
c.1980T= (p.Asn660=)
c.1755T= (p.Asn585=)
c.1587T= (p.Asn529=)
c.1923T= (p.Asn641=)
c.1926T= (p.Asn642=)
c.1650T= (p.Asn550=)
c.1812T= (p.Asn604=)
c.1908T= (p.Asn636=)
n.327T=
c.1869T= (p.Asn623=)
c.1701T= (p.Asn567=)
21g.25897657A>CCA409806561APPn.1947T>G
n.377T>G
n.646T>G
c.1980T>G (p.Asn660Lys)
c.1755T>G (p.Asn585Lys)
c.1587T>G (p.Asn529Lys)
c.1923T>G (p.Asn641Lys)
c.1926T>G (p.Asn642Lys)
c.1650T>G (p.Asn550Lys)
c.1812T>G (p.Asn604Lys)
c.1908T>G (p.Asn636Lys)
n.327T>G
c.1869T>G (p.Asn623Lys)
c.1701T>G (p.Asn567Lys)
21g.25897657A>GCA9987106APPn.1947T>C
n.377T>C
n.646T>C
c.1980T>C (p.Asn660=)
c.1755T>C (p.Asn585=)
c.1587T>C (p.Asn529=)
c.1923T>C (p.Asn641=)
c.1926T>C (p.Asn642=)
c.1650T>C (p.Asn550=)
c.1812T>C (p.Asn604=)
c.1908T>C (p.Asn636=)
n.327T>C
c.1869T>C (p.Asn623=)
c.1701T>C (p.Asn567=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
21g.25897657A>TCA409806562APPn.1947T>A
n.377T>A
n.646T>A
c.1980T>A (p.Asn660Lys)
c.1755T>A (p.Asn585Lys)
c.1587T>A (p.Asn529Lys)
c.1923T>A (p.Asn641Lys)
c.1926T>A (p.Asn642Lys)
c.1650T>A (p.Asn550Lys)
c.1812T>A (p.Asn604Lys)
c.1908T>A (p.Asn636Lys)
n.327T>A
c.1869T>A (p.Asn623Lys)
c.1701T>A (p.Asn567Lys)
21g.25897658T>ACA409806563APPn.1946A>T
n.376A>T
n.645A>T
c.1979A>T (p.Asn660Ile)
c.1754A>T (p.Asn585Ile)
c.1586A>T (p.Asn529Ile)
c.1922A>T (p.Asn641Ile)
c.1925A>T (p.Asn642Ile)
c.1649A>T (p.Asn550Ile)
c.1811A>T (p.Asn604Ile)
c.1907A>T (p.Asn636Ile)
n.326A>T
c.1868A>T (p.Asn623Ile)
c.1700A>T (p.Asn567Ile)
21g.25897658T>CCA409806564APPn.1946A>G
n.376A>G
n.645A>G
c.1979A>G (p.Asn660Ser)
c.1754A>G (p.Asn585Ser)
c.1586A>G (p.Asn529Ser)
c.1922A>G (p.Asn641Ser)
c.1925A>G (p.Asn642Ser)
c.1649A>G (p.Asn550Ser)
c.1811A>G (p.Asn604Ser)
c.1907A>G (p.Asn636Ser)
n.326A>G
c.1868A>G (p.Asn623Ser)
c.1700A>G (p.Asn567Ser)
ClinVar dbSNP
21g.25897658T>GCA409806565APPn.1946A>C
n.376A>C
n.645A>C
c.1979A>C (p.Asn660Thr)
c.1754A>C (p.Asn585Thr)
c.1586A>C (p.Asn529Thr)
c.1922A>C (p.Asn641Thr)
c.1925A>C (p.Asn642Thr)
c.1649A>C (p.Asn550Thr)
c.1811A>C (p.Asn604Thr)
c.1907A>C (p.Asn636Thr)
n.326A>C
c.1868A>C (p.Asn623Thr)
c.1700A>C (p.Asn567Thr)
dbSNP
21g.25897658T=CA2383554951APPn.1946A=
n.376A=
n.645A=
c.1979A= (p.Asn660=)
c.1754A= (p.Asn585=)
c.1586A= (p.Asn529=)
c.1922A= (p.Asn641=)
c.1925A= (p.Asn642=)
c.1649A= (p.Asn550=)
c.1811A= (p.Asn604=)
c.1907A= (p.Asn636=)
n.326A=
c.1868A= (p.Asn623=)
c.1700A= (p.Asn567=)
21g.25897659T>ACA409806566APPn.1945A>T
n.375A>T
n.644A>T
c.1978A>T (p.Asn660Tyr)
c.1753A>T (p.Asn585Tyr)
c.1585A>T (p.Asn529Tyr)
c.1921A>T (p.Asn641Tyr)
c.1924A>T (p.Asn642Tyr)
c.1648A>T (p.Asn550Tyr)
c.1810A>T (p.Asn604Tyr)
c.1906A>T (p.Asn636Tyr)
n.325A>T
c.1867A>T (p.Asn623Tyr)
c.1699A>T (p.Asn567Tyr)
ClinVar dbSNP
21g.25897659T>CCA409806567APPn.1945A>G
n.375A>G
n.644A>G
c.1978A>G (p.Asn660Asp)
c.1753A>G (p.Asn585Asp)
c.1585A>G (p.Asn529Asp)
c.1921A>G (p.Asn641Asp)
c.1924A>G (p.Asn642Asp)
c.1648A>G (p.Asn550Asp)
c.1810A>G (p.Asn604Asp)
c.1906A>G (p.Asn636Asp)
n.325A>G
c.1867A>G (p.Asn623Asp)
c.1699A>G (p.Asn567Asp)
dbSNP gnomAD v3 gnomAD v4
21g.25897659T>GCA9987107APPn.1945A>C
n.375A>C
n.644A>C
c.1978A>C (p.Asn660His)
c.1753A>C (p.Asn585His)
c.1585A>C (p.Asn529His)
c.1921A>C (p.Asn641His)
c.1924A>C (p.Asn642His)
c.1648A>C (p.Asn550His)
c.1810A>C (p.Asn604His)
c.1906A>C (p.Asn636His)
n.325A>C
c.1867A>C (p.Asn623His)
c.1699A>C (p.Asn567His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.25897659T=CA2383554952APPn.1945A=
n.375A=
n.644A=
c.1978A= (p.Asn660=)
c.1753A= (p.Asn585=)
c.1585A= (p.Asn529=)
c.1921A= (p.Asn641=)
c.1924A= (p.Asn642=)
c.1648A= (p.Asn550=)
c.1810A= (p.Asn604=)
c.1906A= (p.Asn636=)
n.325A=
c.1867A= (p.Asn623=)
c.1699A= (p.Asn567=)
21g.25897660T>ACA511686361APPn.1944A>T
n.374A>T
n.643A>T
c.1977A>T (p.Thr659=)
c.1752A>T (p.Thr584=)
c.1584A>T (p.Thr528=)
c.1920A>T (p.Thr640=)
c.1923A>T (p.Thr641=)
c.1647A>T (p.Thr549=)
c.1809A>T (p.Thr603=)
c.1905A>T (p.Thr635=)
n.324A>T
c.1866A>T (p.Thr622=)
c.1698A>T (p.Thr566=)
21g.25897660T>CCA511686368APPn.1944A>G
n.374A>G
n.643A>G
c.1977A>G (p.Thr659=)
c.1752A>G (p.Thr584=)
c.1584A>G (p.Thr528=)
c.1920A>G (p.Thr640=)
c.1923A>G (p.Thr641=)
c.1647A>G (p.Thr549=)
c.1809A>G (p.Thr603=)
c.1905A>G (p.Thr635=)
n.324A>G
c.1866A>G (p.Thr622=)
c.1698A>G (p.Thr566=)
21g.25897660T>GCA511686359APPn.1944A>C
n.374A>C
n.643A>C
c.1977A>C (p.Thr659=)
c.1752A>C (p.Thr584=)
c.1584A>C (p.Thr528=)
c.1920A>C (p.Thr640=)
c.1923A>C (p.Thr641=)
c.1647A>C (p.Thr549=)
c.1809A>C (p.Thr603=)
c.1905A>C (p.Thr635=)
n.324A>C
c.1866A>C (p.Thr622=)
c.1698A>C (p.Thr566=)
21g.25897661G>ACA409806568APPn.1943C>T
n.373C>T
n.642C>T
c.1976C>T (p.Thr659Ile)
c.1751C>T (p.Thr584Ile)
c.1583C>T (p.Thr528Ile)
c.1919C>T (p.Thr640Ile)
c.1922C>T (p.Thr641Ile)
c.1646C>T (p.Thr549Ile)
c.1808C>T (p.Thr603Ile)
c.1904C>T (p.Thr635Ile)
n.323C>T
c.1865C>T (p.Thr622Ile)
c.1697C>T (p.Thr566Ile)
21g.25897661G>CCA409806569APPn.1943C>G
n.373C>G
n.642C>G
c.1976C>G (p.Thr659Arg)
c.1751C>G (p.Thr584Arg)
c.1583C>G (p.Thr528Arg)
c.1919C>G (p.Thr640Arg)
c.1922C>G (p.Thr641Arg)
c.1646C>G (p.Thr549Arg)
c.1808C>G (p.Thr603Arg)
c.1904C>G (p.Thr635Arg)
n.323C>G
c.1865C>G (p.Thr622Arg)
c.1697C>G (p.Thr566Arg)
21g.25897661G=CA2383554953APPn.1943C=
n.373C=
n.642C=
c.1976C= (p.Thr659=)
c.1751C= (p.Thr584=)
c.1583C= (p.Thr528=)
c.1919C= (p.Thr640=)
c.1922C= (p.Thr641=)
c.1646C= (p.Thr549=)
c.1808C= (p.Thr603=)
c.1904C= (p.Thr635=)
n.323C=
c.1865C= (p.Thr622=)
c.1697C= (p.Thr566=)
21g.25897661G>TCA409806570APPn.1943C>A
n.373C>A
n.642C>A
c.1976C>A (p.Thr659Lys)
c.1751C>A (p.Thr584Lys)
c.1583C>A (p.Thr528Lys)
c.1919C>A (p.Thr640Lys)
c.1922C>A (p.Thr641Lys)
c.1646C>A (p.Thr549Lys)
c.1808C>A (p.Thr603Lys)
c.1904C>A (p.Thr635Lys)
n.323C>A
c.1865C>A (p.Thr622Lys)
c.1697C>A (p.Thr566Lys)
dbSNP gnomAD v4
21g.25897662T>ACA409806571APPn.1942A>T
n.372A>T
n.641A>T
c.1975A>T (p.Thr659Ser)
c.1750A>T (p.Thr584Ser)
c.1582A>T (p.Thr528Ser)
c.1918A>T (p.Thr640Ser)
c.1921A>T (p.Thr641Ser)
c.1645A>T (p.Thr549Ser)
c.1807A>T (p.Thr603Ser)
c.1903A>T (p.Thr635Ser)
n.322A>T
c.1864A>T (p.Thr622Ser)
c.1696A>T (p.Thr566Ser)
21g.25897662T>CCA409806572APPn.1942A>G
n.372A>G
n.641A>G
c.1975A>G (p.Thr659Ala)
c.1750A>G (p.Thr584Ala)
c.1582A>G (p.Thr528Ala)
c.1918A>G (p.Thr640Ala)
c.1921A>G (p.Thr641Ala)
c.1645A>G (p.Thr549Ala)
c.1807A>G (p.Thr603Ala)
c.1903A>G (p.Thr635Ala)
n.322A>G
c.1864A>G (p.Thr622Ala)
c.1696A>G (p.Thr566Ala)
21g.25897662T>GCA409806573APPn.1942A>C
n.372A>C
n.641A>C
c.1975A>C (p.Thr659Pro)
c.1750A>C (p.Thr584Pro)
c.1582A>C (p.Thr528Pro)
c.1918A>C (p.Thr640Pro)
c.1921A>C (p.Thr641Pro)
c.1645A>C (p.Thr549Pro)
c.1807A>C (p.Thr603Pro)
c.1903A>C (p.Thr635Pro)
n.322A>C
c.1864A>C (p.Thr622Pro)
c.1696A>C (p.Thr566Pro)
21g.25897663C>ACA409806574APPn.1941G>T
n.371G>T
n.640G>T
c.1974G>T (p.Leu658Phe)
c.1749G>T (p.Leu583Phe)
c.1581G>T (p.Leu527Phe)
c.1917G>T (p.Leu639Phe)
c.1920G>T (p.Leu640Phe)
c.1644G>T (p.Leu548Phe)
c.1806G>T (p.Leu602Phe)
c.1902G>T (p.Leu634Phe)
n.321G>T
c.1863G>T (p.Leu621Phe)
c.1695G>T (p.Leu565Phe)
21g.25897663C=CA2383554954APPn.1941G=
n.371G=
n.640G=
c.1974G= (p.Leu658=)
c.1749G= (p.Leu583=)
c.1581G= (p.Leu527=)
c.1917G= (p.Leu639=)
c.1920G= (p.Leu640=)
c.1644G= (p.Leu548=)
c.1806G= (p.Leu602=)
c.1902G= (p.Leu634=)
n.321G=
c.1863G= (p.Leu621=)
c.1695G= (p.Leu565=)
21g.25897663C>GCA409806575APPn.1941G>C
n.371G>C
n.640G>C
c.1974G>C (p.Leu658Phe)
c.1749G>C (p.Leu583Phe)
c.1581G>C (p.Leu527Phe)
c.1917G>C (p.Leu639Phe)
c.1920G>C (p.Leu640Phe)
c.1644G>C (p.Leu548Phe)
c.1806G>C (p.Leu602Phe)
c.1902G>C (p.Leu634Phe)
n.321G>C
c.1863G>C (p.Leu621Phe)
c.1695G>C (p.Leu565Phe)
21g.25897663C>TCA511686375APPn.1941G>A
n.371G>A
n.640G>A
c.1974G>A (p.Leu658=)
c.1749G>A (p.Leu583=)
c.1581G>A (p.Leu527=)
c.1917G>A (p.Leu639=)
c.1920G>A (p.Leu640=)
c.1644G>A (p.Leu548=)
c.1806G>A (p.Leu602=)
c.1902G>A (p.Leu634=)
n.321G>A
c.1863G>A (p.Leu621=)
c.1695G>A (p.Leu565=)
dbSNP gnomAD v3 gnomAD v4
21g.25897664A>CCA409806576APPn.1940T>G
n.370T>G
n.639T>G
c.1973T>G (p.Leu658Trp)
c.1748T>G (p.Leu583Trp)
c.1580T>G (p.Leu527Trp)
c.1916T>G (p.Leu639Trp)
c.1919T>G (p.Leu640Trp)
c.1643T>G (p.Leu548Trp)
c.1805T>G (p.Leu602Trp)
c.1901T>G (p.Leu634Trp)
n.320T>G
c.1862T>G (p.Leu621Trp)
c.1694T>G (p.Leu565Trp)
21g.25897664A>GCA409806577APPn.1940T>C
n.370T>C
n.639T>C
c.1973T>C (p.Leu658Ser)
c.1748T>C (p.Leu583Ser)
c.1580T>C (p.Leu527Ser)
c.1916T>C (p.Leu639Ser)
c.1919T>C (p.Leu640Ser)
c.1643T>C (p.Leu548Ser)
c.1805T>C (p.Leu602Ser)
c.1901T>C (p.Leu634Ser)
n.320T>C
c.1862T>C (p.Leu621Ser)
c.1694T>C (p.Leu565Ser)
21g.25897664A>TCA409806578APPn.1940T>A
n.370T>A
n.639T>A
c.1973T>A (p.Leu658Ter)
c.1748T>A (p.Leu583Ter)
c.1580T>A (p.Leu527Ter)
c.1916T>A (p.Leu639Ter)
c.1919T>A (p.Leu640Ter)
c.1643T>A (p.Leu548Ter)
c.1805T>A (p.Leu602Ter)
c.1901T>A (p.Leu634Ter)
n.320T>A
c.1862T>A (p.Leu621Ter)
c.1694T>A (p.Leu565Ter)
21g.25897665A>CCA409806580APPn.1939T>G
n.369T>G
n.638T>G
c.1972T>G (p.Leu658Val)
c.1747T>G (p.Leu583Val)
c.1579T>G (p.Leu527Val)
c.1915T>G (p.Leu639Val)
c.1918T>G (p.Leu640Val)
c.1642T>G (p.Leu548Val)
c.1804T>G (p.Leu602Val)
c.1900T>G (p.Leu634Val)
n.319T>G
c.1861T>G (p.Leu621Val)
c.1693T>G (p.Leu565Val)

Number of alleles fetched