| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 21 | g.25891843G>A | CA409805661 | APP | n.2057C>T n.487C>T n.756C>T c.2090C>T (p.Ser697Leu) c.1865C>T (p.Ser622Leu) c.1697C>T (p.Ser566Leu) c.2033C>T (p.Ser678Leu) c.2036C>T (p.Ser679Leu) c.1760C>T (p.Ser587Leu) c.1922C>T (p.Ser641Leu) c.2018C>T (p.Ser673Leu) n.437C>T c.1979C>T (p.Ser660Leu) c.1811C>T (p.Ser604Leu) | |
| 21 | g.25891843G>C | CA409805662 | APP | n.2057C>G n.487C>G n.756C>G c.2090C>G (p.Ser697Ter) c.1865C>G (p.Ser622Ter) c.1697C>G (p.Ser566Ter) c.2033C>G (p.Ser678Ter) c.2036C>G (p.Ser679Ter) c.1760C>G (p.Ser587Ter) c.1922C>G (p.Ser641Ter) c.2018C>G (p.Ser673Ter) n.437C>G c.1979C>G (p.Ser660Ter) c.1811C>G (p.Ser604Ter) | |
| 21 | g.25891843G>T | CA409805663 | APP | n.2057C>A n.487C>A n.756C>A c.2090C>A (p.Ser697Ter) c.1865C>A (p.Ser622Ter) c.1697C>A (p.Ser566Ter) c.2033C>A (p.Ser678Ter) c.2036C>A (p.Ser679Ter) c.1760C>A (p.Ser587Ter) c.1922C>A (p.Ser641Ter) c.2018C>A (p.Ser673Ter) n.437C>A c.1979C>A (p.Ser660Ter) c.1811C>A (p.Ser604Ter) | |
| 21 | g.25891844A>C | CA409805666 | APP | n.2056T>G n.486T>G n.755T>G c.2089T>G (p.Ser697Ala) c.1864T>G (p.Ser622Ala) c.1696T>G (p.Ser566Ala) c.2032T>G (p.Ser678Ala) c.2035T>G (p.Ser679Ala) c.1759T>G (p.Ser587Ala) c.1921T>G (p.Ser641Ala) c.2017T>G (p.Ser673Ala) n.436T>G c.1978T>G (p.Ser660Ala) c.1810T>G (p.Ser604Ala) | |
| 21 | g.25891844A>G | CA409805665 | APP | n.2056T>C n.486T>C n.755T>C c.2089T>C (p.Ser697Pro) c.1864T>C (p.Ser622Pro) c.1696T>C (p.Ser566Pro) c.2032T>C (p.Ser678Pro) c.2035T>C (p.Ser679Pro) c.1759T>C (p.Ser587Pro) c.1921T>C (p.Ser641Pro) c.2017T>C (p.Ser673Pro) n.436T>C c.1978T>C (p.Ser660Pro) c.1810T>C (p.Ser604Pro) | |
| 21 | g.25891844A>T | CA409805664 | APP | n.2056T>A n.486T>A n.755T>A c.2089T>A (p.Ser697Thr) c.1864T>A (p.Ser622Thr) c.1696T>A (p.Ser566Thr) c.2032T>A (p.Ser678Thr) c.2035T>A (p.Ser679Thr) c.1759T>A (p.Ser587Thr) c.1921T>A (p.Ser641Thr) c.2017T>A (p.Ser673Thr) n.436T>A c.1978T>A (p.Ser660Thr) c.1810T>A (p.Ser604Thr) | |
| 21 | g.25891845A>C | CA511686039 | APP | n.2055T>G n.485T>G n.754T>G c.2088T>G (p.Gly696=) c.1863T>G (p.Gly621=) c.1695T>G (p.Gly565=) c.2031T>G (p.Gly677=) c.2034T>G (p.Gly678=) c.1758T>G (p.Gly586=) c.1920T>G (p.Gly640=) c.2016T>G (p.Gly672=) n.435T>G c.1977T>G (p.Gly659=) c.1809T>G (p.Gly603=) | |
| 21 | g.25891845A>G | CA511686040 | APP | n.2055T>C n.485T>C n.754T>C c.2088T>C (p.Gly696=) c.1863T>C (p.Gly621=) c.1695T>C (p.Gly565=) c.2031T>C (p.Gly677=) c.2034T>C (p.Gly678=) c.1758T>C (p.Gly586=) c.1920T>C (p.Gly640=) c.2016T>C (p.Gly672=) n.435T>C c.1977T>C (p.Gly659=) c.1809T>C (p.Gly603=) | |
| 21 | g.25891845A>T | CA511686041 | APP | n.2055T>A n.485T>A n.754T>A c.2088T>A (p.Gly696=) c.1863T>A (p.Gly621=) c.1695T>A (p.Gly565=) c.2031T>A (p.Gly677=) c.2034T>A (p.Gly678=) c.1758T>A (p.Gly586=) c.1920T>A (p.Gly640=) c.2016T>A (p.Gly672=) n.435T>A c.1977T>A (p.Gly659=) c.1809T>A (p.Gly603=) | |
| 21 | g.25891846C>A | CA409805667 | APP | n.2054G>T n.484G>T n.753G>T c.2087G>T (p.Gly696Val) c.1862G>T (p.Gly621Val) c.1694G>T (p.Gly565Val) c.2030G>T (p.Gly677Val) c.2033G>T (p.Gly678Val) c.1757G>T (p.Gly586Val) c.1919G>T (p.Gly640Val) c.2015G>T (p.Gly672Val) n.434G>T c.1976G>T (p.Gly659Val) c.1808G>T (p.Gly603Val) | |
| 21 | g.25891846C= | CA2383551639 | APP | n.2054G= n.484G= n.753G= c.2087G= (p.Gly696=) c.1862G= (p.Gly621=) c.1694G= (p.Gly565=) c.2030G= (p.Gly677=) c.2033G= (p.Gly678=) c.1757G= (p.Gly586=) c.1919G= (p.Gly640=) c.2015G= (p.Gly672=) n.434G= c.1976G= (p.Gly659=) c.1808G= (p.Gly603=) | |
| 21 | g.25891846C>G | CA409805669 | APP | n.2054G>C n.484G>C n.753G>C c.2087G>C (p.Gly696Ala) c.1862G>C (p.Gly621Ala) c.1694G>C (p.Gly565Ala) c.2030G>C (p.Gly677Ala) c.2033G>C (p.Gly678Ala) c.1757G>C (p.Gly586Ala) c.1919G>C (p.Gly640Ala) c.2015G>C (p.Gly672Ala) n.434G>C c.1976G>C (p.Gly659Ala) c.1808G>C (p.Gly603Ala) | |
| 21 | g.25891846C>T | CA409805668 | APP | n.2054G>A n.484G>A n.753G>A c.2087G>A (p.Gly696Asp) c.1862G>A (p.Gly621Asp) c.1694G>A (p.Gly565Asp) c.2030G>A (p.Gly677Asp) c.2033G>A (p.Gly678Asp) c.1757G>A (p.Gly586Asp) c.1919G>A (p.Gly640Asp) c.2015G>A (p.Gly672Asp) n.434G>A c.1976G>A (p.Gly659Asp) c.1808G>A (p.Gly603Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 21 | g.25891847C>A | CA409805670 | APP | n.2053G>T n.483G>T n.752G>T c.2086G>T (p.Gly696Cys) c.1861G>T (p.Gly621Cys) c.1693G>T (p.Gly565Cys) c.2029G>T (p.Gly677Cys) c.2032G>T (p.Gly678Cys) c.1756G>T (p.Gly586Cys) c.1918G>T (p.Gly640Cys) c.2014G>T (p.Gly672Cys) n.433G>T c.1975G>T (p.Gly659Cys) c.1807G>T (p.Gly603Cys) | |
| 21 | g.25891847C>G | CA409805672 | APP | n.2053G>C n.483G>C n.752G>C c.2086G>C (p.Gly696Arg) c.1861G>C (p.Gly621Arg) c.1693G>C (p.Gly565Arg) c.2029G>C (p.Gly677Arg) c.2032G>C (p.Gly678Arg) c.1756G>C (p.Gly586Arg) c.1918G>C (p.Gly640Arg) c.2014G>C (p.Gly672Arg) n.433G>C c.1975G>C (p.Gly659Arg) c.1807G>C (p.Gly603Arg) | |
| 21 | g.25891847C>T | CA409805671 | APP | n.2053G>A n.483G>A n.752G>A c.2086G>A (p.Gly696Ser) c.1861G>A (p.Gly621Ser) c.1693G>A (p.Gly565Ser) c.2029G>A (p.Gly677Ser) c.2032G>A (p.Gly678Ser) c.1756G>A (p.Gly586Ser) c.1918G>A (p.Gly640Ser) c.2014G>A (p.Gly672Ser) n.433G>A c.1975G>A (p.Gly659Ser) c.1807G>A (p.Gly603Ser) | ClinVar |
| 21 | g.25891848C>A | CA511686043 | APP | n.2052G>T n.482G>T n.751G>T c.2085G>T (p.Val695=) c.1860G>T (p.Val620=) c.1692G>T (p.Val564=) c.2028G>T (p.Val676=) c.2031G>T (p.Val677=) c.1755G>T (p.Val585=) c.1917G>T (p.Val639=) c.2013G>T (p.Val671=) n.432G>T c.1974G>T (p.Val658=) c.1806G>T (p.Val602=) | |
| 21 | g.25891848C>G | CA511686042 | APP | n.2052G>C n.482G>C n.751G>C c.2085G>C (p.Val695=) c.1860G>C (p.Val620=) c.1692G>C (p.Val564=) c.2028G>C (p.Val676=) c.2031G>C (p.Val677=) c.1755G>C (p.Val585=) c.1917G>C (p.Val639=) c.2013G>C (p.Val671=) n.432G>C c.1974G>C (p.Val658=) c.1806G>C (p.Val602=) | |
| 21 | g.25891848C>T | CA511686044 | APP | n.2052G>A n.482G>A n.751G>A c.2085G>A (p.Val695=) c.1860G>A (p.Val620=) c.1692G>A (p.Val564=) c.2028G>A (p.Val676=) c.2031G>A (p.Val677=) c.1755G>A (p.Val585=) c.1917G>A (p.Val639=) c.2013G>A (p.Val671=) n.432G>A c.1974G>A (p.Val658=) c.1806G>A (p.Val602=) | gnomAD v4 |
| 21 | g.25891851_25891868del | CA2695230061 | APP | n.2035_2052del n.465_482del n.734_751del c.2068_2085del (p.Phe690_Val695del) c.1843_1860del (p.Phe615_Val620del) c.1675_1692del (p.Phe559_Val564del) c.2011_2028del (p.Phe671_Val676del) c.2014_2031del (p.Phe672_Val677del) c.1738_1755del (p.Phe580_Val585del) c.1900_1917del (p.Phe634_Val639del) c.1996_2013del (p.Phe666_Val671del) n.415_432del c.1957_1974del (p.Phe653_Val658del) c.1789_1806del (p.Phe597_Val602del) | |
| 21 | g.25891849A= | CA2383551640 | APP | n.2051T= n.481T= n.750T= c.2084T= (p.Val695=) c.1859T= (p.Val620=) c.1691T= (p.Val564=) c.2027T= (p.Val676=) c.2030T= (p.Val677=) c.1754T= (p.Val585=) c.1916T= (p.Val639=) c.2012T= (p.Val671=) n.431T= c.1973T= (p.Val658=) c.1805T= (p.Val602=) | |
| 21 | g.25891849A>C | CA409805673 | APP | n.2051T>G n.481T>G n.750T>G c.2084T>G (p.Val695Gly) c.1859T>G (p.Val620Gly) c.1691T>G (p.Val564Gly) c.2027T>G (p.Val676Gly) c.2030T>G (p.Val677Gly) c.1754T>G (p.Val585Gly) c.1916T>G (p.Val639Gly) c.2012T>G (p.Val671Gly) n.431T>G c.1973T>G (p.Val658Gly) c.1805T>G (p.Val602Gly) | dbSNP gnomAD v2 |
| 21 | g.25891849A>G | CA409805675 | APP | n.2051T>C n.481T>C n.750T>C c.2084T>C (p.Val695Ala) c.1859T>C (p.Val620Ala) c.1691T>C (p.Val564Ala) c.2027T>C (p.Val676Ala) c.2030T>C (p.Val677Ala) c.1754T>C (p.Val585Ala) c.1916T>C (p.Val639Ala) c.2012T>C (p.Val671Ala) n.431T>C c.1973T>C (p.Val658Ala) c.1805T>C (p.Val602Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 21 | g.25891849A>T | CA409805674 | APP | n.2051T>A n.481T>A n.750T>A c.2084T>A (p.Val695Glu) c.1859T>A (p.Val620Glu) c.1691T>A (p.Val564Glu) c.2027T>A (p.Val676Glu) c.2030T>A (p.Val677Glu) c.1754T>A (p.Val585Glu) c.1916T>A (p.Val639Glu) c.2012T>A (p.Val671Glu) n.431T>A c.1973T>A (p.Val658Glu) c.1805T>A (p.Val602Glu) | |
| 21 | g.25891850C>A | CA409805676 | APP | n.2050G>T n.480G>T n.749G>T c.2083G>T (p.Val695Leu) c.1858G>T (p.Val620Leu) c.1690G>T (p.Val564Leu) c.2026G>T (p.Val676Leu) c.2029G>T (p.Val677Leu) c.1753G>T (p.Val585Leu) c.1915G>T (p.Val639Leu) c.2011G>T (p.Val671Leu) n.430G>T c.1972G>T (p.Val658Leu) c.1804G>T (p.Val602Leu) | |
| 21 | g.25891850C= | CA2383551641 | APP | n.2050G= n.480G= n.749G= c.2083G= (p.Val695=) c.1858G= (p.Val620=) c.1690G= (p.Val564=) c.2026G= (p.Val676=) c.2029G= (p.Val677=) c.1753G= (p.Val585=) c.1915G= (p.Val639=) c.2011G= (p.Val671=) n.430G= c.1972G= (p.Val658=) c.1804G= (p.Val602=) | |
| 21 | g.25891850C>G | CA409805677 | APP | n.2050G>C n.480G>C n.749G>C c.2083G>C (p.Val695Leu) c.1858G>C (p.Val620Leu) c.1690G>C (p.Val564Leu) c.2026G>C (p.Val676Leu) c.2029G>C (p.Val677Leu) c.1753G>C (p.Val585Leu) c.1915G>C (p.Val639Leu) c.2011G>C (p.Val671Leu) n.430G>C c.1972G>C (p.Val658Leu) c.1804G>C (p.Val602Leu) | |
| 21 | g.25891850C>T | CA409805678 | APP | n.2050G>A n.480G>A n.749G>A c.2083G>A (p.Val695Met) c.1858G>A (p.Val620Met) c.1690G>A (p.Val564Met) c.2026G>A (p.Val676Met) c.2029G>A (p.Val677Met) c.1753G>A (p.Val585Met) c.1915G>A (p.Val639Met) c.2011G>A (p.Val671Met) n.430G>A c.1972G>A (p.Val658Met) c.1804G>A (p.Val602Met) | dbSNP gnomAD v4 |
| 21 | g.25891851A>C | CA409805679 | APP | n.2049T>G n.479T>G n.748T>G c.2082T>G (p.Asp694Glu) c.1857T>G (p.Asp619Glu) c.1689T>G (p.Asp563Glu) c.2025T>G (p.Asp675Glu) c.2028T>G (p.Asp676Glu) c.1752T>G (p.Asp584Glu) c.1914T>G (p.Asp638Glu) c.2010T>G (p.Asp670Glu) n.429T>G c.1971T>G (p.Asp657Glu) c.1803T>G (p.Asp601Glu) | gnomAD v4 |
| 21 | g.25891851A>G | CA511686045 | APP | n.2049T>C n.479T>C n.748T>C c.2082T>C (p.Asp694=) c.1857T>C (p.Asp619=) c.1689T>C (p.Asp563=) c.2025T>C (p.Asp675=) c.2028T>C (p.Asp676=) c.1752T>C (p.Asp584=) c.1914T>C (p.Asp638=) c.2010T>C (p.Asp670=) n.429T>C c.1971T>C (p.Asp657=) c.1803T>C (p.Asp601=) | |
| 21 | g.25891851A>T | CA409805680 | APP | n.2049T>A n.479T>A n.748T>A c.2082T>A (p.Asp694Glu) c.1857T>A (p.Asp619Glu) c.1689T>A (p.Asp563Glu) c.2025T>A (p.Asp675Glu) c.2028T>A (p.Asp676Glu) c.1752T>A (p.Asp584Glu) c.1914T>A (p.Asp638Glu) c.2010T>A (p.Asp670Glu) n.429T>A c.1971T>A (p.Asp657Glu) c.1803T>A (p.Asp601Glu) | |
| 21 | g.25891852T>A | CA409805681 | APP | n.2048A>T n.478A>T n.747A>T c.2081A>T (p.Asp694Val) c.1856A>T (p.Asp619Val) c.1688A>T (p.Asp563Val) c.2024A>T (p.Asp675Val) c.2027A>T (p.Asp676Val) c.1751A>T (p.Asp584Val) c.1913A>T (p.Asp638Val) c.2009A>T (p.Asp670Val) n.428A>T c.1970A>T (p.Asp657Val) c.1802A>T (p.Asp601Val) | |
| 21 | g.25891852T>C | CA409805682 | APP | n.2048A>G n.478A>G n.747A>G c.2081A>G (p.Asp694Gly) c.1856A>G (p.Asp619Gly) c.1688A>G (p.Asp563Gly) c.2024A>G (p.Asp675Gly) c.2027A>G (p.Asp676Gly) c.1751A>G (p.Asp584Gly) c.1913A>G (p.Asp638Gly) c.2009A>G (p.Asp670Gly) n.428A>G c.1970A>G (p.Asp657Gly) c.1802A>G (p.Asp601Gly) | |
| 21 | g.25891852T>G | CA409805683 | APP | n.2048A>C n.478A>C n.747A>C c.2081A>C (p.Asp694Ala) c.1856A>C (p.Asp619Ala) c.1688A>C (p.Asp563Ala) c.2024A>C (p.Asp675Ala) c.2027A>C (p.Asp676Ala) c.1751A>C (p.Asp584Ala) c.1913A>C (p.Asp638Ala) c.2009A>C (p.Asp670Ala) n.428A>C c.1970A>C (p.Asp657Ala) c.1802A>C (p.Asp601Ala) | |
| 21 | g.25891855_25891857del | CA2654122495 | APP | n.2046_2048del n.476_478del n.745_747del c.2079_2081del (p.Glu693del) c.1854_1856del (p.Glu618del) c.1686_1688del (p.Glu562del) c.2022_2024del (p.Glu674del) c.2025_2027del (p.Glu675del) c.1749_1751del (p.Glu583del) c.1911_1913del (p.Glu637del) c.2007_2009del (p.Glu669del) n.426_428del c.1968_1970del (p.Glu656del) c.1800_1802del (p.Glu600del) | gnomAD v4 |
| 21 | g.25891853C>A | CA409805684 | APP | n.2047G>T n.477G>T n.746G>T c.2080G>T (p.Asp694Tyr) c.1855G>T (p.Asp619Tyr) c.1687G>T (p.Asp563Tyr) c.2023G>T (p.Asp675Tyr) c.2026G>T (p.Asp676Tyr) c.1750G>T (p.Asp584Tyr) c.1912G>T (p.Asp638Tyr) c.2008G>T (p.Asp670Tyr) n.427G>T c.1969G>T (p.Asp657Tyr) c.1801G>T (p.Asp601Tyr) | |
| 21 | g.25891853C= | CA2383551642 | APP | n.2047G= n.477G= n.746G= c.2080G= (p.Asp694=) c.1855G= (p.Asp619=) c.1687G= (p.Asp563=) c.2023G= (p.Asp675=) c.2026G= (p.Asp676=) c.1750G= (p.Asp584=) c.1912G= (p.Asp638=) c.2008G= (p.Asp670=) n.427G= c.1969G= (p.Asp657=) c.1801G= (p.Asp601=) | |
| 21 | g.25891853C>G | CA409805685 | APP | n.2047G>C n.477G>C n.746G>C c.2080G>C (p.Asp694His) c.1855G>C (p.Asp619His) c.1687G>C (p.Asp563His) c.2023G>C (p.Asp675His) c.2026G>C (p.Asp676His) c.1750G>C (p.Asp584His) c.1912G>C (p.Asp638His) c.2008G>C (p.Asp670His) n.427G>C c.1969G>C (p.Asp657His) c.1801G>C (p.Asp601His) | |
| 21 | g.25891853C>T | CA127804 | APP | n.2047G>A n.477G>A n.746G>A c.2080G>A (p.Asp694Asn) c.1855G>A (p.Asp619Asn) c.1687G>A (p.Asp563Asn) c.2023G>A (p.Asp675Asn) c.2026G>A (p.Asp676Asn) c.1750G>A (p.Asp584Asn) c.1912G>A (p.Asp638Asn) c.2008G>A (p.Asp670Asn) n.427G>A c.1969G>A (p.Asp657Asn) c.1801G>A (p.Asp601Asn) | ClinVar dbSNP gnomAD v4 |
| 21 | g.25891854T>A | CA9987062 | APP | n.2046A>T n.476A>T n.745A>T c.2079A>T (p.Glu693Asp) c.1854A>T (p.Glu618Asp) c.1686A>T (p.Glu562Asp) c.2022A>T (p.Glu674Asp) c.2025A>T (p.Glu675Asp) c.1749A>T (p.Glu583Asp) c.1911A>T (p.Glu637Asp) c.2007A>T (p.Glu669Asp) n.426A>T c.1968A>T (p.Glu656Asp) c.1800A>T (p.Glu600Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 21 | g.25891854T>C | CA511686046 | APP | n.2046A>G n.476A>G n.745A>G c.2079A>G (p.Glu693=) c.1854A>G (p.Glu618=) c.1686A>G (p.Glu562=) c.2022A>G (p.Glu674=) c.2025A>G (p.Glu675=) c.1749A>G (p.Glu583=) c.1911A>G (p.Glu637=) c.2007A>G (p.Glu669=) n.426A>G c.1968A>G (p.Glu656=) c.1800A>G (p.Glu600=) | ClinVar dbSNP |
| 21 | g.25891854T>G | CA409805686 | APP | n.2046A>C n.476A>C n.745A>C c.2079A>C (p.Glu693Asp) c.1854A>C (p.Glu618Asp) c.1686A>C (p.Glu562Asp) c.2022A>C (p.Glu674Asp) c.2025A>C (p.Glu675Asp) c.1749A>C (p.Glu583Asp) c.1911A>C (p.Glu637Asp) c.2007A>C (p.Glu669Asp) n.426A>C c.1968A>C (p.Glu656Asp) c.1800A>C (p.Glu600Asp) | |
| 21 | g.25891854T= | CA2383551643 | APP | n.2046A= n.476A= n.745A= c.2079A= (p.Glu693=) c.1854A= (p.Glu618=) c.1686A= (p.Glu562=) c.2022A= (p.Glu674=) c.2025A= (p.Glu675=) c.1749A= (p.Glu583=) c.1911A= (p.Glu637=) c.2007A= (p.Glu669=) n.426A= c.1968A= (p.Glu656=) c.1800A= (p.Glu600=) | |
| 21 | g.25891855T>A | CA409805687 | APP | n.2045A>T n.475A>T n.744A>T c.2078A>T (p.Glu693Val) c.1853A>T (p.Glu618Val) c.1685A>T (p.Glu562Val) c.2021A>T (p.Glu674Val) c.2024A>T (p.Glu675Val) c.1748A>T (p.Glu583Val) c.1910A>T (p.Glu637Val) c.2006A>T (p.Glu669Val) n.425A>T c.1967A>T (p.Glu656Val) c.1799A>T (p.Glu600Val) | |
| 21 | g.25891855T>C | CA127801 | APP | n.2045A>G n.475A>G n.744A>G c.2078A>G (p.Glu693Gly) c.1853A>G (p.Glu618Gly) c.1685A>G (p.Glu562Gly) c.2021A>G (p.Glu674Gly) c.2024A>G (p.Glu675Gly) c.1748A>G (p.Glu583Gly) c.1910A>G (p.Glu637Gly) c.2006A>G (p.Glu669Gly) n.425A>G c.1967A>G (p.Glu656Gly) c.1799A>G (p.Glu600Gly) | ClinVar dbSNP |
| 21 | g.25891855T>G | CA409805688 | APP | n.2045A>C n.475A>C n.744A>C c.2078A>C (p.Glu693Ala) c.1853A>C (p.Glu618Ala) c.1685A>C (p.Glu562Ala) c.2021A>C (p.Glu674Ala) c.2024A>C (p.Glu675Ala) c.1748A>C (p.Glu583Ala) c.1910A>C (p.Glu637Ala) c.2006A>C (p.Glu669Ala) n.425A>C c.1967A>C (p.Glu656Ala) c.1799A>C (p.Glu600Ala) | |
| 21 | g.25891855T= | CA2383551644 | APP | n.2045A= n.475A= n.744A= c.2078A= (p.Glu693=) c.1853A= (p.Glu618=) c.1685A= (p.Glu562=) c.2021A= (p.Glu674=) c.2024A= (p.Glu675=) c.1748A= (p.Glu583=) c.1910A= (p.Glu637=) c.2006A= (p.Glu669=) n.425A= c.1967A= (p.Glu656=) c.1799A= (p.Glu600=) | |
| 21 | g.25891856C>A | CA409805689 | APP | n.2044G>T n.474G>T n.743G>T c.2077G>T (p.Glu693Ter) c.1852G>T (p.Glu618Ter) c.1684G>T (p.Glu562Ter) c.2020G>T (p.Glu674Ter) c.2023G>T (p.Glu675Ter) c.1747G>T (p.Glu583Ter) c.1909G>T (p.Glu637Ter) c.2005G>T (p.Glu669Ter) n.424G>T c.1966G>T (p.Glu656Ter) c.1798G>T (p.Glu600Ter) | |
| 21 | g.25891856C= | CA2383551645 | APP | n.2044G= n.474G= n.743G= c.2077G= (p.Glu693=) c.1852G= (p.Glu618=) c.1684G= (p.Glu562=) c.2020G= (p.Glu674=) c.2023G= (p.Glu675=) c.1747G= (p.Glu583=) c.1909G= (p.Glu637=) c.2005G= (p.Glu669=) n.424G= c.1966G= (p.Glu656=) c.1798G= (p.Glu600=) | |
| 21 | g.25891856C>G | CA127790 | APP | n.2044G>C n.474G>C n.743G>C c.2077G>C (p.Glu693Gln) c.1852G>C (p.Glu618Gln) c.1684G>C (p.Glu562Gln) c.2020G>C (p.Glu674Gln) c.2023G>C (p.Glu675Gln) c.1747G>C (p.Glu583Gln) c.1909G>C (p.Glu637Gln) c.2005G>C (p.Glu669Gln) n.424G>C c.1966G>C (p.Glu656Gln) c.1798G>C (p.Glu600Gln) | ClinVar dbSNP |