Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.25897646_25897648dupCA748247763APPn.1960_1962dup
n.390_392dup
n.659_661dup
c.1993_1995dup (p.Glu665_Ile666insGlu)
c.1768_1770dup (p.Glu590_Ile591insGlu)
c.1600_1602dup (p.Glu534_Ile535insGlu)
c.1936_1938dup (p.Glu646_Ile647insGlu)
c.1939_1941dup (p.Glu647_Ile648insGlu)
c.1663_1665dup (p.Glu555_Ile556insGlu)
c.1825_1827dup (p.Glu609_Ile610insGlu)
c.1921_1923dup (p.Glu641_Ile642insGlu)
n.340_342dup
c.1882_1884dup (p.Glu628_Ile629insGlu)
c.1714_1716dup (p.Glu572_Ile573insGlu)
dbSNP gnomAD v4
21g.25897646_25897648delCA9987101APPn.1960_1962del
n.390_392del
n.659_661del
c.1993_1995del (p.Glu665del)
c.1768_1770del (p.Glu590del)
c.1600_1602del (p.Glu534del)
c.1936_1938del (p.Glu646del)
c.1939_1941del (p.Glu647del)
c.1663_1665del (p.Glu555del)
c.1825_1827del (p.Glu609del)
c.1921_1923del (p.Glu641del)
n.340_342del
c.1882_1884del (p.Glu628del)
c.1714_1716del (p.Glu572del)
dbSNP ExAC gnomAD v2 gnomAD v4
21g.25897648C>ACA511686315APPn.1956G>T
n.386G>T
n.655G>T
c.1989G>T (p.Thr663=)
c.1764G>T (p.Thr588=)
c.1596G>T (p.Thr532=)
c.1932G>T (p.Thr644=)
c.1935G>T (p.Thr645=)
c.1659G>T (p.Thr553=)
c.1821G>T (p.Thr607=)
c.1917G>T (p.Thr639=)
n.336G>T
c.1878G>T (p.Thr626=)
c.1710G>T (p.Thr570=)
21g.25897648C=CA2383554943APPn.1956G=
n.386G=
n.655G=
c.1989G= (p.Thr663=)
c.1764G= (p.Thr588=)
c.1596G= (p.Thr532=)
c.1932G= (p.Thr644=)
c.1935G= (p.Thr645=)
c.1659G= (p.Thr553=)
c.1821G= (p.Thr607=)
c.1917G= (p.Thr639=)
n.336G=
c.1878G= (p.Thr626=)
c.1710G= (p.Thr570=)
21g.25897648C>GCA9987103APPn.1956G>C
n.386G>C
n.655G>C
c.1989G>C (p.Thr663=)
c.1764G>C (p.Thr588=)
c.1596G>C (p.Thr532=)
c.1932G>C (p.Thr644=)
c.1935G>C (p.Thr645=)
c.1659G>C (p.Thr553=)
c.1821G>C (p.Thr607=)
c.1917G>C (p.Thr639=)
n.336G>C
c.1878G>C (p.Thr626=)
c.1710G>C (p.Thr570=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.25897648C>TCA319103543APPn.1956G>A
n.386G>A
n.655G>A
c.1989G>A (p.Thr663=)
c.1764G>A (p.Thr588=)
c.1596G>A (p.Thr532=)
c.1932G>A (p.Thr644=)
c.1935G>A (p.Thr645=)
c.1659G>A (p.Thr553=)
c.1821G>A (p.Thr607=)
c.1917G>A (p.Thr639=)
n.336G>A
c.1878G>A (p.Thr626=)
c.1710G>A (p.Thr570=)
dbSNP gnomAD v4
21g.25897649G>ACA9987104APPn.1955C>T
n.385C>T
n.654C>T
c.1988C>T (p.Thr663Met)
c.1763C>T (p.Thr588Met)
c.1595C>T (p.Thr532Met)
c.1931C>T (p.Thr644Met)
c.1934C>T (p.Thr645Met)
c.1658C>T (p.Thr553Met)
c.1820C>T (p.Thr607Met)
c.1916C>T (p.Thr639Met)
n.335C>T
c.1877C>T (p.Thr626Met)
c.1709C>T (p.Thr570Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.25897649G>CCA409806542APPn.1955C>G
n.385C>G
n.654C>G
c.1988C>G (p.Thr663Arg)
c.1763C>G (p.Thr588Arg)
c.1595C>G (p.Thr532Arg)
c.1931C>G (p.Thr644Arg)
c.1934C>G (p.Thr645Arg)
c.1658C>G (p.Thr553Arg)
c.1820C>G (p.Thr607Arg)
c.1916C>G (p.Thr639Arg)
n.335C>G
c.1877C>G (p.Thr626Arg)
c.1709C>G (p.Thr570Arg)
21g.25897649G=CA2383554944APPn.1955C=
n.385C=
n.654C=
c.1988C= (p.Thr663=)
c.1763C= (p.Thr588=)
c.1595C= (p.Thr532=)
c.1931C= (p.Thr644=)
c.1934C= (p.Thr645=)
c.1658C= (p.Thr553=)
c.1820C= (p.Thr607=)
c.1916C= (p.Thr639=)
n.335C=
c.1877C= (p.Thr626=)
c.1709C= (p.Thr570=)
21g.25897649G>TCA409806544APPn.1955C>A
n.385C>A
n.654C>A
c.1988C>A (p.Thr663Lys)
c.1763C>A (p.Thr588Lys)
c.1595C>A (p.Thr532Lys)
c.1931C>A (p.Thr644Lys)
c.1934C>A (p.Thr645Lys)
c.1658C>A (p.Thr553Lys)
c.1820C>A (p.Thr607Lys)
c.1916C>A (p.Thr639Lys)
n.335C>A
c.1877C>A (p.Thr626Lys)
c.1709C>A (p.Thr570Lys)
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.25897650T>ACA409806545APPn.1954A>T
n.384A>T
n.653A>T
c.1987A>T (p.Thr663Ser)
c.1762A>T (p.Thr588Ser)
c.1594A>T (p.Thr532Ser)
c.1930A>T (p.Thr644Ser)
c.1933A>T (p.Thr645Ser)
c.1657A>T (p.Thr553Ser)
c.1819A>T (p.Thr607Ser)
c.1915A>T (p.Thr639Ser)
n.334A>T
c.1876A>T (p.Thr626Ser)
c.1708A>T (p.Thr570Ser)
21g.25897650T>CCA409806546APPn.1954A>G
n.384A>G
n.653A>G
c.1987A>G (p.Thr663Ala)
c.1762A>G (p.Thr588Ala)
c.1594A>G (p.Thr532Ala)
c.1930A>G (p.Thr644Ala)
c.1933A>G (p.Thr645Ala)
c.1657A>G (p.Thr553Ala)
c.1819A>G (p.Thr607Ala)
c.1915A>G (p.Thr639Ala)
n.334A>G
c.1876A>G (p.Thr626Ala)
c.1708A>G (p.Thr570Ala)
gnomAD v4
21g.25897650T>GCA409806547APPn.1954A>C
n.384A>C
n.653A>C
c.1987A>C (p.Thr663Pro)
c.1762A>C (p.Thr588Pro)
c.1594A>C (p.Thr532Pro)
c.1930A>C (p.Thr644Pro)
c.1933A>C (p.Thr645Pro)
c.1657A>C (p.Thr553Pro)
c.1819A>C (p.Thr607Pro)
c.1915A>C (p.Thr639Pro)
n.334A>C
c.1876A>C (p.Thr626Pro)
c.1708A>C (p.Thr570Pro)
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.25897651C>ACA409806548APPn.1953G>T
n.383G>T
n.652G>T
c.1986G>T (p.Lys662Asn)
c.1761G>T (p.Lys587Asn)
c.1593G>T (p.Lys531Asn)
c.1929G>T (p.Lys643Asn)
c.1932G>T (p.Lys644Asn)
c.1656G>T (p.Lys552Asn)
c.1818G>T (p.Lys606Asn)
c.1914G>T (p.Lys638Asn)
n.333G>T
c.1875G>T (p.Lys625Asn)
c.1707G>T (p.Lys569Asn)
21g.25897651C>GCA409806549APPn.1953G>C
n.383G>C
n.652G>C
c.1986G>C (p.Lys662Asn)
c.1761G>C (p.Lys587Asn)
c.1593G>C (p.Lys531Asn)
c.1929G>C (p.Lys643Asn)
c.1932G>C (p.Lys644Asn)
c.1656G>C (p.Lys552Asn)
c.1818G>C (p.Lys606Asn)
c.1914G>C (p.Lys638Asn)
n.333G>C
c.1875G>C (p.Lys625Asn)
c.1707G>C (p.Lys569Asn)
21g.25897651C>TCA511686327APPn.1953G>A
n.383G>A
n.652G>A
c.1986G>A (p.Lys662=)
c.1761G>A (p.Lys587=)
c.1593G>A (p.Lys531=)
c.1929G>A (p.Lys643=)
c.1932G>A (p.Lys644=)
c.1656G>A (p.Lys552=)
c.1818G>A (p.Lys606=)
c.1914G>A (p.Lys638=)
n.333G>A
c.1875G>A (p.Lys625=)
c.1707G>A (p.Lys569=)
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=)

Number of alleles fetched