Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.25897646_25897648dupCA748247763APPc.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)
c.1882_1884dup (p.Glu628_Ile629insGlu)
c.1714_1716dup (p.Glu572_Ile573insGlu)
dbSNP
21g.25897642_25897644delCA9987101APPc.1989_1991del (p.Glu665del)
c.1764_1766del (p.Glu590del)
c.1596_1598del (p.Glu534del)
c.1932_1934del (p.Glu646del)
c.1935_1937del (p.Glu647del)
c.1659_1661del (p.Glu555del)
c.1821_1823del (p.Glu609del)
c.1917_1919del (p.Glu641del)
c.1878_1880del (p.Glu628del)
c.1710_1712del (p.Glu572del)
dbSNP dbSNP ExAC gnomAD
21g.25897647C>ACA409806541APPc.1990G>T (p.Glu664Ter)
c.1765G>T (p.Glu589Ter)
c.1597G>T (p.Glu533Ter)
c.1933G>T (p.Glu645Ter)
c.1936G>T (p.Glu646Ter)
c.1660G>T (p.Glu554Ter)
c.1822G>T (p.Glu608Ter)
c.1918G>T (p.Glu640Ter)
c.1879G>T (p.Glu627Ter)
c.1711G>T (p.Glu571Ter)
21g.25897647C>GCA409806537APPc.1990G>C (p.Glu664Gln)
c.1765G>C (p.Glu589Gln)
c.1597G>C (p.Glu533Gln)
c.1933G>C (p.Glu645Gln)
c.1936G>C (p.Glu646Gln)
c.1660G>C (p.Glu554Gln)
c.1822G>C (p.Glu608Gln)
c.1918G>C (p.Glu640Gln)
c.1879G>C (p.Glu627Gln)
c.1711G>C (p.Glu571Gln)
COSMIC
21g.25897647C>TCA409806540APPc.1990G>A (p.Glu664Lys)
c.1765G>A (p.Glu589Lys)
c.1597G>A (p.Glu533Lys)
c.1933G>A (p.Glu645Lys)
c.1936G>A (p.Glu646Lys)
c.1660G>A (p.Glu554Lys)
c.1822G>A (p.Glu608Lys)
c.1918G>A (p.Glu640Lys)
c.1879G>A (p.Glu627Lys)
c.1711G>A (p.Glu571Lys)
21g.25897648C>ACA511686315APPc.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=)
c.1878G>T (p.Thr626=)
c.1710G>T (p.Thr570=)
21g.25897648C>GCA9987103APPc.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=)
c.1878G>C (p.Thr626=)
c.1710G>C (p.Thr570=)
dbSNP ExAC gnomAD
21g.25897648C>TCA319103543APPc.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=)
c.1878G>A (p.Thr626=)
c.1710G>A (p.Thr570=)
dbSNP
21g.25897649G>ACA9987104APPc.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)
c.1877C>T (p.Thr626Met)
c.1709C>T (p.Thr570Met)
dbSNP ExAC gnomAD
21g.25897649G>CCA409806542APPc.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)
c.1877C>G (p.Thr626Arg)
c.1709C>G (p.Thr570Arg)
21g.25897649G>TCA409806544APPc.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)
c.1877C>A (p.Thr626Lys)
c.1709C>A (p.Thr570Lys)
21g.25897650T>ACA409806545APPc.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)
c.1876A>T (p.Thr626Ser)
c.1708A>T (p.Thr570Ser)
21g.25897650T>CCA409806546APPc.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)
c.1876A>G (p.Thr626Ala)
c.1708A>G (p.Thr570Ala)
21g.25897650T>GCA409806547APPc.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)
c.1876A>C (p.Thr626Pro)
c.1708A>C (p.Thr570Pro)
21g.25897651C>ACA409806548APPc.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)
c.1875G>T (p.Lys625Asn)
c.1707G>T (p.Lys569Asn)
21g.25897651C>GCA409806549APPc.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)
c.1875G>C (p.Lys625Asn)
c.1707G>C (p.Lys569Asn)
21g.25897651C>TCA511686327APPc.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=)
c.1875G>A (p.Lys625=)
c.1707G>A (p.Lys569=)
21g.25897652T>ACA409806550APPc.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)
c.1874A>T (p.Lys625Met)
c.1706A>T (p.Lys569Met)
21g.25897652T>CCA409806551APPc.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)
c.1874A>G (p.Lys625Arg)
c.1706A>G (p.Lys569Arg)
21g.25897652T>GCA409806552APPc.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)
c.1874A>C (p.Lys625Thr)
c.1706A>C (p.Lys569Thr)
21g.25897653T>ACA409806553APPc.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)
c.1873A>T (p.Lys625Ter)
c.1705A>T (p.Lys569Ter)
21g.25897653T>CCA409806555APPc.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)
c.1873A>G (p.Lys625Glu)
c.1705A>G (p.Lys569Glu)
21g.25897653T>GCA409806554APPc.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)
c.1873A>C (p.Lys625Gln)
c.1705A>C (p.Lys569Gln)
21g.25897654G>ACA511686342APPc.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=)
c.1872C>T (p.Ile624=)
c.1704C>T (p.Ile568=)
21g.25897654G>CCA409806556APPc.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)
c.1872C>G (p.Ile624Met)
c.1704C>G (p.Ile568Met)
21g.25897654G>TCA511686341APPc.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=)
c.1872C>A (p.Ile624=)
c.1704C>A (p.Ile568=)
21g.25897655A>CCA409806557APPc.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)
c.1871T>G (p.Ile624Ser)
c.1703T>G (p.Ile568Ser)
21g.25897655A>GCA9987105APPc.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)
c.1871T>C (p.Ile624Thr)
c.1703T>C (p.Ile568Thr)
dbSNP ExAC gnomAD
21g.25897655A>TCA409806558APPc.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)
c.1871T>A (p.Ile624Asn)
c.1703T>A (p.Ile568Asn)
21g.25897656T>ACA409806559APPc.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)
c.1870A>T (p.Ile624Phe)
c.1702A>T (p.Ile568Phe)
21g.25897656T>CCA319103568APPc.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)
c.1870A>G (p.Ile624Val)
c.1702A>G (p.Ile568Val)
dbSNP gnomAD
21g.25897656T>GCA409806560APPc.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)
c.1870A>C (p.Ile624Leu)
c.1702A>C (p.Ile568Leu)
21g.25897657A>CCA409806561APPc.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)
c.1869T>G (p.Asn623Lys)
c.1701T>G (p.Asn567Lys)
21g.25897657A>GCA9987106APPc.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=)
c.1869T>C (p.Asn623=)
c.1701T>C (p.Asn567=)
dbSNP ExAC gnomAD
21g.25897657A>TCA409806562APPc.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)
c.1869T>A (p.Asn623Lys)
c.1701T>A (p.Asn567Lys)
21g.25897658T>ACA409806563APPc.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)
c.1868A>T (p.Asn623Ile)
c.1700A>T (p.Asn567Ile)
21g.25897658T>CCA409806564APPc.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)
c.1868A>G (p.Asn623Ser)
c.1700A>G (p.Asn567Ser)
21g.25897658T>GCA409806565APPc.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)
c.1868A>C (p.Asn623Thr)
c.1700A>C (p.Asn567Thr)
21g.25897659T>ACA409806566APPc.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)
c.1867A>T (p.Asn623Tyr)
c.1699A>T (p.Asn567Tyr)
21g.25897659T>CCA409806567APPc.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)
c.1867A>G (p.Asn623Asp)
c.1699A>G (p.Asn567Asp)
21g.25897659T>GCA9987107APPc.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)
c.1867A>C (p.Asn623His)
c.1699A>C (p.Asn567His)
dbSNP ExAC gnomAD
21g.25897660T>ACA511686361APPc.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=)
c.1866A>T (p.Thr622=)
c.1698A>T (p.Thr566=)
21g.25897660T>CCA511686368APPc.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=)
c.1866A>G (p.Thr622=)
c.1698A>G (p.Thr566=)
21g.25897660T>GCA511686359APPc.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=)
c.1866A>C (p.Thr622=)
c.1698A>C (p.Thr566=)
21g.25897661G>ACA409806568APPc.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)
c.1865C>T (p.Thr622Ile)
c.1697C>T (p.Thr566Ile)
21g.25897661G>CCA409806569APPc.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)
c.1865C>G (p.Thr622Arg)
c.1697C>G (p.Thr566Arg)
21g.25897661G>TCA409806570APPc.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)
c.1865C>A (p.Thr622Lys)
c.1697C>A (p.Thr566Lys)
21g.25897662T>ACA409806571APPc.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)
c.1864A>T (p.Thr622Ser)
c.1696A>T (p.Thr566Ser)
21g.25897662T>CCA409806572APPc.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)
c.1864A>G (p.Thr622Ala)
c.1696A>G (p.Thr566Ala)
21g.25897662T>GCA409806573APPc.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)
c.1864A>C (p.Thr622Pro)
c.1696A>C (p.Thr566Pro)

Number of alleles fetched