| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 21 | g.25891828A>C | CA409805628 | APP | n.2072T>G n.502T>G n.771T>G c.2105T>G (p.Ile702Ser) c.1880T>G (p.Ile627Ser) c.1712T>G (p.Ile571Ser) c.2048T>G (p.Ile683Ser) c.2051T>G (p.Ile684Ser) c.1775T>G (p.Ile592Ser) c.1937T>G (p.Ile646Ser) c.2033T>G (p.Ile678Ser) n.452T>G c.1994T>G (p.Ile665Ser) c.1826T>G (p.Ile609Ser) | |
| 21 | g.25891828A>G | CA409805629 | APP | n.2072T>C n.502T>C n.771T>C c.2105T>C (p.Ile702Thr) c.1880T>C (p.Ile627Thr) c.1712T>C (p.Ile571Thr) c.2048T>C (p.Ile683Thr) c.2051T>C (p.Ile684Thr) c.1775T>C (p.Ile592Thr) c.1937T>C (p.Ile646Thr) c.2033T>C (p.Ile678Thr) n.452T>C c.1994T>C (p.Ile665Thr) c.1826T>C (p.Ile609Thr) | |
| 21 | g.25891828A>T | CA409805630 | APP | n.2072T>A n.502T>A n.771T>A c.2105T>A (p.Ile702Asn) c.1880T>A (p.Ile627Asn) c.1712T>A (p.Ile571Asn) c.2048T>A (p.Ile683Asn) c.2051T>A (p.Ile684Asn) c.1775T>A (p.Ile592Asn) c.1937T>A (p.Ile646Asn) c.2033T>A (p.Ile678Asn) n.452T>A c.1994T>A (p.Ile665Asn) c.1826T>A (p.Ile609Asn) | |
| 21 | g.25891829_25891833dup | CA2654122471 | APP | n.2068_2072dup n.498_502dup n.767_771dup c.2101_2105dup (p.Ile702MetfsTer13) c.1876_1880dup (p.Ile627MetfsTer13) c.1708_1712dup (p.Ile571MetfsTer13) c.2044_2048dup (p.Ile683MetfsTer13) c.2047_2051dup (p.Ile684MetfsTer13) c.1771_1775dup (p.Ile592MetfsTer13) c.1933_1937dup (p.Ile646MetfsTer13) c.2029_2033dup (p.Ile678MetfsTer13) n.448_452dup c.1990_1994dup (p.Ile665MetfsTer13) c.1822_1826dup (p.Ile609MetfsTer13) | gnomAD v4 |
| 21 | g.25891829T>A | CA409805631 | APP | n.2071A>T n.501A>T n.770A>T c.2104A>T (p.Ile702Phe) c.1879A>T (p.Ile627Phe) c.1711A>T (p.Ile571Phe) c.2047A>T (p.Ile683Phe) c.2050A>T (p.Ile684Phe) c.1774A>T (p.Ile592Phe) c.1936A>T (p.Ile646Phe) c.2032A>T (p.Ile678Phe) n.451A>T c.1993A>T (p.Ile665Phe) c.1825A>T (p.Ile609Phe) | |
| 21 | g.25891829T>C | CA9987061 | APP | n.2071A>G n.501A>G n.770A>G c.2104A>G (p.Ile702Val) c.1879A>G (p.Ile627Val) c.1711A>G (p.Ile571Val) c.2047A>G (p.Ile683Val) c.2050A>G (p.Ile684Val) c.1774A>G (p.Ile592Val) c.1936A>G (p.Ile646Val) c.2032A>G (p.Ile678Val) n.451A>G c.1993A>G (p.Ile665Val) c.1825A>G (p.Ile609Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 21 | g.25891829T>G | CA409805632 | APP | n.2071A>C n.501A>C n.770A>C c.2104A>C (p.Ile702Leu) c.1879A>C (p.Ile627Leu) c.1711A>C (p.Ile571Leu) c.2047A>C (p.Ile683Leu) c.2050A>C (p.Ile684Leu) c.1774A>C (p.Ile592Leu) c.1936A>C (p.Ile646Leu) c.2032A>C (p.Ile678Leu) n.451A>C c.1993A>C (p.Ile665Leu) c.1825A>C (p.Ile609Leu) | |
| 21 | g.25891829T= | CA2383551635 | APP | n.2071A= n.501A= n.770A= c.2104A= (p.Ile702=) c.1879A= (p.Ile627=) c.1711A= (p.Ile571=) c.2047A= (p.Ile683=) c.2050A= (p.Ile684=) c.1774A= (p.Ile592=) c.1936A= (p.Ile646=) c.2032A= (p.Ile678=) n.451A= c.1993A= (p.Ile665=) c.1825A= (p.Ile609=) | |
| 21 | g.25891830T>A | CA511686030 | APP | n.2070A>T n.500A>T n.769A>T c.2103A>T (p.Ala701=) c.1878A>T (p.Ala626=) c.1710A>T (p.Ala570=) c.2046A>T (p.Ala682=) c.2049A>T (p.Ala683=) c.1773A>T (p.Ala591=) c.1935A>T (p.Ala645=) c.2031A>T (p.Ala677=) n.450A>T c.1992A>T (p.Ala664=) c.1824A>T (p.Ala608=) | |
| 21 | g.25891830T>C | CA511686028 | APP | n.2070A>G n.500A>G n.769A>G c.2103A>G (p.Ala701=) c.1878A>G (p.Ala626=) c.1710A>G (p.Ala570=) c.2046A>G (p.Ala682=) c.2049A>G (p.Ala683=) c.1773A>G (p.Ala591=) c.1935A>G (p.Ala645=) c.2031A>G (p.Ala677=) n.450A>G c.1992A>G (p.Ala664=) c.1824A>G (p.Ala608=) | |
| 21 | g.25891830T>G | CA511686029 | APP | n.2070A>C n.500A>C n.769A>C c.2103A>C (p.Ala701=) c.1878A>C (p.Ala626=) c.1710A>C (p.Ala570=) c.2046A>C (p.Ala682=) c.2049A>C (p.Ala683=) c.1773A>C (p.Ala591=) c.1935A>C (p.Ala645=) c.2031A>C (p.Ala677=) n.450A>C c.1992A>C (p.Ala664=) c.1824A>C (p.Ala608=) | dbSNP |
| 21 | g.25891830T= | CA2383551636 | APP | n.2070A= n.500A= n.769A= c.2103A= (p.Ala701=) c.1878A= (p.Ala626=) c.1710A= (p.Ala570=) c.2046A= (p.Ala682=) c.2049A= (p.Ala683=) c.1773A= (p.Ala591=) c.1935A= (p.Ala645=) c.2031A= (p.Ala677=) n.450A= c.1992A= (p.Ala664=) c.1824A= (p.Ala608=) | |
| 21 | g.25891831G>A | CA409805634 | APP | n.2069C>T n.499C>T n.768C>T c.2102C>T (p.Ala701Val) c.1877C>T (p.Ala626Val) c.1709C>T (p.Ala570Val) c.2045C>T (p.Ala682Val) c.2048C>T (p.Ala683Val) c.1772C>T (p.Ala591Val) c.1934C>T (p.Ala645Val) c.2030C>T (p.Ala677Val) n.449C>T c.1991C>T (p.Ala664Val) c.1823C>T (p.Ala608Val) | COSMIC |
| 21 | g.25891831G>C | CA409805635 | APP | n.2069C>G n.499C>G n.768C>G c.2102C>G (p.Ala701Gly) c.1877C>G (p.Ala626Gly) c.1709C>G (p.Ala570Gly) c.2045C>G (p.Ala682Gly) c.2048C>G (p.Ala683Gly) c.1772C>G (p.Ala591Gly) c.1934C>G (p.Ala645Gly) c.2030C>G (p.Ala677Gly) n.449C>G c.1991C>G (p.Ala664Gly) c.1823C>G (p.Ala608Gly) | |
| 21 | g.25891831G>T | CA409805633 | APP | n.2069C>A n.499C>A n.768C>A c.2102C>A (p.Ala701Glu) c.1877C>A (p.Ala626Glu) c.1709C>A (p.Ala570Glu) c.2045C>A (p.Ala682Glu) c.2048C>A (p.Ala683Glu) c.1772C>A (p.Ala591Glu) c.1934C>A (p.Ala645Glu) c.2030C>A (p.Ala677Glu) n.449C>A c.1991C>A (p.Ala664Glu) c.1823C>A (p.Ala608Glu) | gnomAD v4 |
| 21 | g.25891832C>A | CA409805636 | APP | n.2068G>T n.498G>T n.767G>T c.2101G>T (p.Ala701Ser) c.1876G>T (p.Ala626Ser) c.1708G>T (p.Ala570Ser) c.2044G>T (p.Ala682Ser) c.2047G>T (p.Ala683Ser) c.1771G>T (p.Ala591Ser) c.1933G>T (p.Ala645Ser) c.2029G>T (p.Ala677Ser) n.448G>T c.1990G>T (p.Ala664Ser) c.1822G>T (p.Ala608Ser) | |
| 21 | g.25891832C>G | CA409805637 | APP | n.2068G>C n.498G>C n.767G>C c.2101G>C (p.Ala701Pro) c.1876G>C (p.Ala626Pro) c.1708G>C (p.Ala570Pro) c.2044G>C (p.Ala682Pro) c.2047G>C (p.Ala683Pro) c.1771G>C (p.Ala591Pro) c.1933G>C (p.Ala645Pro) c.2029G>C (p.Ala677Pro) n.448G>C c.1990G>C (p.Ala664Pro) c.1822G>C (p.Ala608Pro) | |
| 21 | g.25891832C>T | CA409805638 | APP | n.2068G>A n.498G>A n.767G>A c.2101G>A (p.Ala701Thr) c.1876G>A (p.Ala626Thr) c.1708G>A (p.Ala570Thr) c.2044G>A (p.Ala682Thr) c.2047G>A (p.Ala683Thr) c.1771G>A (p.Ala591Thr) c.1933G>A (p.Ala645Thr) c.2029G>A (p.Ala677Thr) n.448G>A c.1990G>A (p.Ala664Thr) c.1822G>A (p.Ala608Thr) | gnomAD v4 |
| 21 | g.25891833A= | CA2383551637 | APP | n.2067T= n.497T= n.766T= c.2100T= (p.Gly700=) c.1875T= (p.Gly625=) c.1707T= (p.Gly569=) c.2043T= (p.Gly681=) c.2046T= (p.Gly682=) c.1770T= (p.Gly590=) c.1932T= (p.Gly644=) c.2028T= (p.Gly676=) n.447T= c.1989T= (p.Gly663=) c.1821T= (p.Gly607=) | |
| 21 | g.25891833A>C | CA511686031 | APP | n.2067T>G n.497T>G n.766T>G c.2100T>G (p.Gly700=) c.1875T>G (p.Gly625=) c.1707T>G (p.Gly569=) c.2043T>G (p.Gly681=) c.2046T>G (p.Gly682=) c.1770T>G (p.Gly590=) c.1932T>G (p.Gly644=) c.2028T>G (p.Gly676=) n.447T>G c.1989T>G (p.Gly663=) c.1821T>G (p.Gly607=) | |
| 21 | g.25891833A>G | CA511686032 | APP | n.2067T>C n.497T>C n.766T>C c.2100T>C (p.Gly700=) c.1875T>C (p.Gly625=) c.1707T>C (p.Gly569=) c.2043T>C (p.Gly681=) c.2046T>C (p.Gly682=) c.1770T>C (p.Gly590=) c.1932T>C (p.Gly644=) c.2028T>C (p.Gly676=) n.447T>C c.1989T>C (p.Gly663=) c.1821T>C (p.Gly607=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 21 | g.25891833A>T | CA511686033 | APP | n.2067T>A n.497T>A n.766T>A c.2100T>A (p.Gly700=) c.1875T>A (p.Gly625=) c.1707T>A (p.Gly569=) c.2043T>A (p.Gly681=) c.2046T>A (p.Gly682=) c.1770T>A (p.Gly590=) c.1932T>A (p.Gly644=) c.2028T>A (p.Gly676=) n.447T>A c.1989T>A (p.Gly663=) c.1821T>A (p.Gly607=) | |
| 21 | g.25891834C>A | CA409805639 | APP | n.2066G>T n.496G>T n.765G>T c.2099G>T (p.Gly700Val) c.1874G>T (p.Gly625Val) c.1706G>T (p.Gly569Val) c.2042G>T (p.Gly681Val) c.2045G>T (p.Gly682Val) c.1769G>T (p.Gly590Val) c.1931G>T (p.Gly644Val) c.2027G>T (p.Gly676Val) n.446G>T c.1988G>T (p.Gly663Val) c.1820G>T (p.Gly607Val) | |
| 21 | g.25891834C>G | CA409805640 | APP | n.2066G>C n.496G>C n.765G>C c.2099G>C (p.Gly700Ala) c.1874G>C (p.Gly625Ala) c.1706G>C (p.Gly569Ala) c.2042G>C (p.Gly681Ala) c.2045G>C (p.Gly682Ala) c.1769G>C (p.Gly590Ala) c.1931G>C (p.Gly644Ala) c.2027G>C (p.Gly676Ala) n.446G>C c.1988G>C (p.Gly663Ala) c.1820G>C (p.Gly607Ala) | |
| 21 | g.25891834C>T | CA409805641 | APP | n.2066G>A n.496G>A n.765G>A c.2099G>A (p.Gly700Asp) c.1874G>A (p.Gly625Asp) c.1706G>A (p.Gly569Asp) c.2042G>A (p.Gly681Asp) c.2045G>A (p.Gly682Asp) c.1769G>A (p.Gly590Asp) c.1931G>A (p.Gly644Asp) c.2027G>A (p.Gly676Asp) n.446G>A c.1988G>A (p.Gly663Asp) c.1820G>A (p.Gly607Asp) | |
| 21 | g.25891835C>A | CA409805644 | APP | n.2065G>T n.495G>T n.764G>T c.2098G>T (p.Gly700Cys) c.1873G>T (p.Gly625Cys) c.1705G>T (p.Gly569Cys) c.2041G>T (p.Gly681Cys) c.2044G>T (p.Gly682Cys) c.1768G>T (p.Gly590Cys) c.1930G>T (p.Gly644Cys) c.2026G>T (p.Gly676Cys) n.445G>T c.1987G>T (p.Gly663Cys) c.1819G>T (p.Gly607Cys) | |
| 21 | g.25891835C>G | CA409805642 | APP | n.2065G>C n.495G>C n.764G>C c.2098G>C (p.Gly700Arg) c.1873G>C (p.Gly625Arg) c.1705G>C (p.Gly569Arg) c.2041G>C (p.Gly681Arg) c.2044G>C (p.Gly682Arg) c.1768G>C (p.Gly590Arg) c.1930G>C (p.Gly644Arg) c.2026G>C (p.Gly676Arg) n.445G>C c.1987G>C (p.Gly663Arg) c.1819G>C (p.Gly607Arg) | |
| 21 | g.25891835C>T | CA409805643 | APP | n.2065G>A n.495G>A n.764G>A c.2098G>A (p.Gly700Ser) c.1873G>A (p.Gly625Ser) c.1705G>A (p.Gly569Ser) c.2041G>A (p.Gly681Ser) c.2044G>A (p.Gly682Ser) c.1768G>A (p.Gly590Ser) c.1930G>A (p.Gly644Ser) c.2026G>A (p.Gly676Ser) n.445G>A c.1987G>A (p.Gly663Ser) c.1819G>A (p.Gly607Ser) | |
| 21 | g.25891836T>A | CA409805645 | APP | n.2064A>T n.494A>T n.763A>T c.2097A>T (p.Lys699Asn) c.1872A>T (p.Lys624Asn) c.1704A>T (p.Lys568Asn) c.2040A>T (p.Lys680Asn) c.2043A>T (p.Lys681Asn) c.1767A>T (p.Lys589Asn) c.1929A>T (p.Lys643Asn) c.2025A>T (p.Lys675Asn) n.444A>T c.1986A>T (p.Lys662Asn) c.1818A>T (p.Lys606Asn) | |
| 21 | g.25891836T>C | CA511686034 | APP | n.2064A>G n.494A>G n.763A>G c.2097A>G (p.Lys699=) c.1872A>G (p.Lys624=) c.1704A>G (p.Lys568=) c.2040A>G (p.Lys680=) c.2043A>G (p.Lys681=) c.1767A>G (p.Lys589=) c.1929A>G (p.Lys643=) c.2025A>G (p.Lys675=) n.444A>G c.1986A>G (p.Lys662=) c.1818A>G (p.Lys606=) | |
| 21 | g.25891836T>G | CA409805646 | APP | n.2064A>C n.494A>C n.763A>C c.2097A>C (p.Lys699Asn) c.1872A>C (p.Lys624Asn) c.1704A>C (p.Lys568Asn) c.2040A>C (p.Lys680Asn) c.2043A>C (p.Lys681Asn) c.1767A>C (p.Lys589Asn) c.1929A>C (p.Lys643Asn) c.2025A>C (p.Lys675Asn) n.444A>C c.1986A>C (p.Lys662Asn) c.1818A>C (p.Lys606Asn) | |
| 21 | g.25891837T>A | CA409805647 | APP | n.2063A>T n.493A>T n.762A>T c.2096A>T (p.Lys699Ile) c.1871A>T (p.Lys624Ile) c.1703A>T (p.Lys568Ile) c.2039A>T (p.Lys680Ile) c.2042A>T (p.Lys681Ile) c.1766A>T (p.Lys589Ile) c.1928A>T (p.Lys643Ile) c.2024A>T (p.Lys675Ile) n.443A>T c.1985A>T (p.Lys662Ile) c.1817A>T (p.Lys606Ile) | |
| 21 | g.25891837T>C | CA409805648 | APP | n.2063A>G n.493A>G n.762A>G c.2096A>G (p.Lys699Arg) c.1871A>G (p.Lys624Arg) c.1703A>G (p.Lys568Arg) c.2039A>G (p.Lys680Arg) c.2042A>G (p.Lys681Arg) c.1766A>G (p.Lys589Arg) c.1928A>G (p.Lys643Arg) c.2024A>G (p.Lys675Arg) n.443A>G c.1985A>G (p.Lys662Arg) c.1817A>G (p.Lys606Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 21 | g.25891837T>G | CA409805649 | APP | n.2063A>C n.493A>C n.762A>C c.2096A>C (p.Lys699Thr) c.1871A>C (p.Lys624Thr) c.1703A>C (p.Lys568Thr) c.2039A>C (p.Lys680Thr) c.2042A>C (p.Lys681Thr) c.1766A>C (p.Lys589Thr) c.1928A>C (p.Lys643Thr) c.2024A>C (p.Lys675Thr) n.443A>C c.1985A>C (p.Lys662Thr) c.1817A>C (p.Lys606Thr) | |
| 21 | g.25891837T= | CA2383551638 | APP | n.2063A= n.493A= n.762A= c.2096A= (p.Lys699=) c.1871A= (p.Lys624=) c.1703A= (p.Lys568=) c.2039A= (p.Lys680=) c.2042A= (p.Lys681=) c.1766A= (p.Lys589=) c.1928A= (p.Lys643=) c.2024A= (p.Lys675=) n.443A= c.1985A= (p.Lys662=) c.1817A= (p.Lys606=) | |
| 21 | g.25891838T>A | CA409805650 | APP | n.2062A>T n.492A>T n.761A>T c.2095A>T (p.Lys699Ter) c.1870A>T (p.Lys624Ter) c.1702A>T (p.Lys568Ter) c.2038A>T (p.Lys680Ter) c.2041A>T (p.Lys681Ter) c.1765A>T (p.Lys589Ter) c.1927A>T (p.Lys643Ter) c.2023A>T (p.Lys675Ter) n.442A>T c.1984A>T (p.Lys662Ter) c.1816A>T (p.Lys606Ter) | |
| 21 | g.25891838T>C | CA409805652 | APP | n.2062A>G n.492A>G n.761A>G c.2095A>G (p.Lys699Glu) c.1870A>G (p.Lys624Glu) c.1702A>G (p.Lys568Glu) c.2038A>G (p.Lys680Glu) c.2041A>G (p.Lys681Glu) c.1765A>G (p.Lys589Glu) c.1927A>G (p.Lys643Glu) c.2023A>G (p.Lys675Glu) n.442A>G c.1984A>G (p.Lys662Glu) c.1816A>G (p.Lys606Glu) | gnomAD v4 |
| 21 | g.25891838T>G | CA409805651 | APP | n.2062A>C n.492A>C n.761A>C c.2095A>C (p.Lys699Gln) c.1870A>C (p.Lys624Gln) c.1702A>C (p.Lys568Gln) c.2038A>C (p.Lys680Gln) c.2041A>C (p.Lys681Gln) c.1765A>C (p.Lys589Gln) c.1927A>C (p.Lys643Gln) c.2023A>C (p.Lys675Gln) n.442A>C c.1984A>C (p.Lys662Gln) c.1816A>C (p.Lys606Gln) | |
| 21 | g.25891839G>A | CA511686035 | APP | n.2061C>T n.491C>T n.760C>T c.2094C>T (p.Asn698=) c.1869C>T (p.Asn623=) c.1701C>T (p.Asn567=) c.2037C>T (p.Asn679=) c.2040C>T (p.Asn680=) c.1764C>T (p.Asn588=) c.1926C>T (p.Asn642=) c.2022C>T (p.Asn674=) n.441C>T c.1983C>T (p.Asn661=) c.1815C>T (p.Asn605=) | |
| 21 | g.25891839G>C | CA409805653 | APP | n.2061C>G n.491C>G n.760C>G c.2094C>G (p.Asn698Lys) c.1869C>G (p.Asn623Lys) c.1701C>G (p.Asn567Lys) c.2037C>G (p.Asn679Lys) c.2040C>G (p.Asn680Lys) c.1764C>G (p.Asn588Lys) c.1926C>G (p.Asn642Lys) c.2022C>G (p.Asn674Lys) n.441C>G c.1983C>G (p.Asn661Lys) c.1815C>G (p.Asn605Lys) | gnomAD v4 |
| 21 | g.25891839G>T | CA409805654 | APP | n.2061C>A n.491C>A n.760C>A c.2094C>A (p.Asn698Lys) c.1869C>A (p.Asn623Lys) c.1701C>A (p.Asn567Lys) c.2037C>A (p.Asn679Lys) c.2040C>A (p.Asn680Lys) c.1764C>A (p.Asn588Lys) c.1926C>A (p.Asn642Lys) c.2022C>A (p.Asn674Lys) n.441C>A c.1983C>A (p.Asn661Lys) c.1815C>A (p.Asn605Lys) | |
| 21 | g.25891840T>A | CA409805655 | APP | n.2060A>T n.490A>T n.759A>T c.2093A>T (p.Asn698Ile) c.1868A>T (p.Asn623Ile) c.1700A>T (p.Asn567Ile) c.2036A>T (p.Asn679Ile) c.2039A>T (p.Asn680Ile) c.1763A>T (p.Asn588Ile) c.1925A>T (p.Asn642Ile) c.2021A>T (p.Asn674Ile) n.440A>T c.1982A>T (p.Asn661Ile) c.1814A>T (p.Asn605Ile) | |
| 21 | g.25891840T>C | CA409805656 | APP | n.2060A>G n.490A>G n.759A>G c.2093A>G (p.Asn698Ser) c.1868A>G (p.Asn623Ser) c.1700A>G (p.Asn567Ser) c.2036A>G (p.Asn679Ser) c.2039A>G (p.Asn680Ser) c.1763A>G (p.Asn588Ser) c.1925A>G (p.Asn642Ser) c.2021A>G (p.Asn674Ser) n.440A>G c.1982A>G (p.Asn661Ser) c.1814A>G (p.Asn605Ser) | |
| 21 | g.25891840T>G | CA409805657 | APP | n.2060A>C n.490A>C n.759A>C c.2093A>C (p.Asn698Thr) c.1868A>C (p.Asn623Thr) c.1700A>C (p.Asn567Thr) c.2036A>C (p.Asn679Thr) c.2039A>C (p.Asn680Thr) c.1763A>C (p.Asn588Thr) c.1925A>C (p.Asn642Thr) c.2021A>C (p.Asn674Thr) n.440A>C c.1982A>C (p.Asn661Thr) c.1814A>C (p.Asn605Thr) | |
| 21 | g.25891841T>A | CA409805658 | APP | n.2059A>T n.489A>T n.758A>T c.2092A>T (p.Asn698Tyr) c.1867A>T (p.Asn623Tyr) c.1699A>T (p.Asn567Tyr) c.2035A>T (p.Asn679Tyr) c.2038A>T (p.Asn680Tyr) c.1762A>T (p.Asn588Tyr) c.1924A>T (p.Asn642Tyr) c.2020A>T (p.Asn674Tyr) n.439A>T c.1981A>T (p.Asn661Tyr) c.1813A>T (p.Asn605Tyr) | |
| 21 | g.25891841T>C | CA409805659 | APP | n.2059A>G n.489A>G n.758A>G c.2092A>G (p.Asn698Asp) c.1867A>G (p.Asn623Asp) c.1699A>G (p.Asn567Asp) c.2035A>G (p.Asn679Asp) c.2038A>G (p.Asn680Asp) c.1762A>G (p.Asn588Asp) c.1924A>G (p.Asn642Asp) c.2020A>G (p.Asn674Asp) n.439A>G c.1981A>G (p.Asn661Asp) c.1813A>G (p.Asn605Asp) | |
| 21 | g.25891841T>G | CA409805660 | APP | n.2059A>C n.489A>C n.758A>C c.2092A>C (p.Asn698His) c.1867A>C (p.Asn623His) c.1699A>C (p.Asn567His) c.2035A>C (p.Asn679His) c.2038A>C (p.Asn680His) c.1762A>C (p.Asn588His) c.1924A>C (p.Asn642His) c.2020A>C (p.Asn674His) n.439A>C c.1981A>C (p.Asn661His) c.1813A>C (p.Asn605His) | |
| 21 | g.25891842T>A | CA511686038 | APP | n.2058A>T n.488A>T n.757A>T c.2091A>T (p.Ser697=) c.1866A>T (p.Ser622=) c.1698A>T (p.Ser566=) c.2034A>T (p.Ser678=) c.2037A>T (p.Ser679=) c.1761A>T (p.Ser587=) c.1923A>T (p.Ser641=) c.2019A>T (p.Ser673=) n.438A>T c.1980A>T (p.Ser660=) c.1812A>T (p.Ser604=) | |
| 21 | g.25891842T>C | CA511686036 | APP | n.2058A>G n.488A>G n.757A>G c.2091A>G (p.Ser697=) c.1866A>G (p.Ser622=) c.1698A>G (p.Ser566=) c.2034A>G (p.Ser678=) c.2037A>G (p.Ser679=) c.1761A>G (p.Ser587=) c.1923A>G (p.Ser641=) c.2019A>G (p.Ser673=) n.438A>G c.1980A>G (p.Ser660=) c.1812A>G (p.Ser604=) | |
| 21 | g.25891842T>G | CA511686037 | APP | n.2058A>C n.488A>C n.757A>C c.2091A>C (p.Ser697=) c.1866A>C (p.Ser622=) c.1698A>C (p.Ser566=) c.2034A>C (p.Ser678=) c.2037A>C (p.Ser679=) c.1761A>C (p.Ser587=) c.1923A>C (p.Ser641=) c.2019A>C (p.Ser673=) n.438A>C c.1980A>C (p.Ser660=) c.1812A>C (p.Ser604=) |