| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 21 | g.25897579T>A | CA409806237 | APP | n.2025A>T n.455A>T n.724A>T c.2058A>T (p.Gln686His) c.1833A>T (p.Gln611His) c.1665A>T (p.Gln555His) c.2001A>T (p.Gln667His) c.2004A>T (p.Gln668His) c.1728A>T (p.Gln576His) c.1890A>T (p.Gln630His) c.1986A>T (p.Gln662His) n.405A>T c.1947A>T (p.Gln649His) c.1779A>T (p.Gln593His) | COSMIC |
| 21 | g.25897579T>C | CA511686138 | APP | n.2025A>G n.455A>G n.724A>G c.2058A>G (p.Gln686=) c.1833A>G (p.Gln611=) c.1665A>G (p.Gln555=) c.2001A>G (p.Gln667=) c.2004A>G (p.Gln668=) c.1728A>G (p.Gln576=) c.1890A>G (p.Gln630=) c.1986A>G (p.Gln662=) n.405A>G c.1947A>G (p.Gln649=) c.1779A>G (p.Gln593=) | dbSNP gnomAD v3 gnomAD v4 |
| 21 | g.25897579T>G | CA409806239 | APP | n.2025A>C n.455A>C n.724A>C c.2058A>C (p.Gln686His) c.1833A>C (p.Gln611His) c.1665A>C (p.Gln555His) c.2001A>C (p.Gln667His) c.2004A>C (p.Gln668His) c.1728A>C (p.Gln576His) c.1890A>C (p.Gln630His) c.1986A>C (p.Gln662His) n.405A>C c.1947A>C (p.Gln649His) c.1779A>C (p.Gln593His) | |
| 21 | g.25897579T= | CA2383554904 | APP | n.2025A= n.455A= n.724A= c.2058A= (p.Gln686=) c.1833A= (p.Gln611=) c.1665A= (p.Gln555=) c.2001A= (p.Gln667=) c.2004A= (p.Gln668=) c.1728A= (p.Gln576=) c.1890A= (p.Gln630=) c.1986A= (p.Gln662=) n.405A= c.1947A= (p.Gln649=) c.1779A= (p.Gln593=) | |
| 21 | g.25897579_25897582delinsTTGA | CA2383554903 | APP | n.2022_2025delinsTCAA n.452_455delinsTCAA n.721_724delinsTCAA c.2055_2058delinsTCAA (p.His685=) c.1830_1833delinsTCAA (p.His610=) c.1662_1665delinsTCAA (p.His554=) c.1998_2001delinsTCAA (p.His666=) c.2001_2004delinsTCAA (p.His667=) c.1725_1728delinsTCAA (p.His575=) c.1887_1890delinsTCAA (p.His629=) c.1983_1986delinsTCAA (p.His661=) n.402_405delinsTCAA c.1944_1947delinsTCAA (p.His648=) c.1776_1779delinsTCAA (p.His592=) | |
| 21 | g.25897580T>A | CA409806241 | APP | n.2024A>T n.454A>T n.723A>T c.2057A>T (p.Gln686Leu) c.1832A>T (p.Gln611Leu) c.1664A>T (p.Gln555Leu) c.2000A>T (p.Gln667Leu) c.2003A>T (p.Gln668Leu) c.1727A>T (p.Gln576Leu) c.1889A>T (p.Gln630Leu) c.1985A>T (p.Gln662Leu) n.404A>T c.1946A>T (p.Gln649Leu) c.1778A>T (p.Gln593Leu) | |
| 21 | g.25897580T>C | CA409806242 | APP | n.2024A>G n.454A>G n.723A>G c.2057A>G (p.Gln686Arg) c.1832A>G (p.Gln611Arg) c.1664A>G (p.Gln555Arg) c.2000A>G (p.Gln667Arg) c.2003A>G (p.Gln668Arg) c.1727A>G (p.Gln576Arg) c.1889A>G (p.Gln630Arg) c.1985A>G (p.Gln662Arg) n.404A>G c.1946A>G (p.Gln649Arg) c.1778A>G (p.Gln593Arg) | |
| 21 | g.25897580T>G | CA409806244 | APP | n.2024A>C n.454A>C n.723A>C c.2057A>C (p.Gln686Pro) c.1832A>C (p.Gln611Pro) c.1664A>C (p.Gln555Pro) c.2000A>C (p.Gln667Pro) c.2003A>C (p.Gln668Pro) c.1727A>C (p.Gln576Pro) c.1889A>C (p.Gln630Pro) c.1985A>C (p.Gln662Pro) n.404A>C c.1946A>C (p.Gln649Pro) c.1778A>C (p.Gln593Pro) | COSMIC |
| 21 | g.25897586_25897588del | CA511686140 | APP | n.2022_2024del n.452_454del n.721_723del c.2055_2057del (p.His685del) c.1830_1832del (p.His610del) c.1662_1664del (p.His554del) c.1998_2000del (p.His666del) c.2001_2003del (p.His667del) c.1725_1727del (p.His575del) c.1887_1889del (p.His629del) c.1983_1985del (p.His661del) n.402_404del c.1944_1946del (p.His648del) c.1776_1778del (p.His592del) | dbSNP gnomAD v2 |
| 21 | g.25897581G>A | CA409806246 | APP | n.2023C>T n.453C>T n.722C>T c.2056C>T (p.Gln686Ter) c.1831C>T (p.Gln611Ter) c.1663C>T (p.Gln555Ter) c.1999C>T (p.Gln667Ter) c.2002C>T (p.Gln668Ter) c.1726C>T (p.Gln576Ter) c.1888C>T (p.Gln630Ter) c.1984C>T (p.Gln662Ter) n.403C>T c.1945C>T (p.Gln649Ter) c.1777C>T (p.Gln593Ter) | |
| 21 | g.25897581G>C | CA409806248 | APP | n.2023C>G n.453C>G n.722C>G c.2056C>G (p.Gln686Glu) c.1831C>G (p.Gln611Glu) c.1663C>G (p.Gln555Glu) c.1999C>G (p.Gln667Glu) c.2002C>G (p.Gln668Glu) c.1726C>G (p.Gln576Glu) c.1888C>G (p.Gln630Glu) c.1984C>G (p.Gln662Glu) n.403C>G c.1945C>G (p.Gln649Glu) c.1777C>G (p.Gln593Glu) | dbSNP gnomAD v4 |
| 21 | g.25897581G= | CA2383554905 | APP | n.2023C= n.453C= n.722C= c.2056C= (p.Gln686=) c.1831C= (p.Gln611=) c.1663C= (p.Gln555=) c.1999C= (p.Gln667=) c.2002C= (p.Gln668=) c.1726C= (p.Gln576=) c.1888C= (p.Gln630=) c.1984C= (p.Gln662=) n.403C= c.1945C= (p.Gln649=) c.1777C= (p.Gln593=) | |
| 21 | g.25897581G>T | CA409806250 | APP | n.2023C>A n.453C>A n.722C>A c.2056C>A (p.Gln686Lys) c.1831C>A (p.Gln611Lys) c.1663C>A (p.Gln555Lys) c.1999C>A (p.Gln667Lys) c.2002C>A (p.Gln668Lys) c.1726C>A (p.Gln576Lys) c.1888C>A (p.Gln630Lys) c.1984C>A (p.Gln662Lys) n.403C>A c.1945C>A (p.Gln649Lys) c.1777C>A (p.Gln593Lys) | COSMIC |
| 21 | g.25897582A>C | CA409806252 | APP | n.2022T>G n.452T>G n.721T>G c.2055T>G (p.His685Gln) c.1830T>G (p.His610Gln) c.1662T>G (p.His554Gln) c.1998T>G (p.His666Gln) c.2001T>G (p.His667Gln) c.1725T>G (p.His575Gln) c.1887T>G (p.His629Gln) c.1983T>G (p.His661Gln) n.402T>G c.1944T>G (p.His648Gln) c.1776T>G (p.His592Gln) | |
| 21 | g.25897582A>G | CA511686143 | APP | n.2022T>C n.452T>C n.721T>C c.2055T>C (p.His685=) c.1830T>C (p.His610=) c.1662T>C (p.His554=) c.1998T>C (p.His666=) c.2001T>C (p.His667=) c.1725T>C (p.His575=) c.1887T>C (p.His629=) c.1983T>C (p.His661=) n.402T>C c.1944T>C (p.His648=) c.1776T>C (p.His592=) | |
| 21 | g.25897582A>T | CA409806253 | APP | n.2022T>A n.452T>A n.721T>A c.2055T>A (p.His685Gln) c.1830T>A (p.His610Gln) c.1662T>A (p.His554Gln) c.1998T>A (p.His666Gln) c.2001T>A (p.His667Gln) c.1725T>A (p.His575Gln) c.1887T>A (p.His629Gln) c.1983T>A (p.His661Gln) n.402T>A c.1944T>A (p.His648Gln) c.1776T>A (p.His592Gln) | |
| 21 | g.25897583T>A | CA409806258 | APP | n.2021A>T n.451A>T n.720A>T c.2054A>T (p.His685Leu) c.1829A>T (p.His610Leu) c.1661A>T (p.His554Leu) c.1997A>T (p.His666Leu) c.2000A>T (p.His667Leu) c.1724A>T (p.His575Leu) c.1886A>T (p.His629Leu) c.1982A>T (p.His661Leu) n.401A>T c.1943A>T (p.His648Leu) c.1775A>T (p.His592Leu) | |
| 21 | g.25897583T>C | CA9987087 | APP | n.2021A>G n.451A>G n.720A>G c.2054A>G (p.His685Arg) c.1829A>G (p.His610Arg) c.1661A>G (p.His554Arg) c.1997A>G (p.His666Arg) c.2000A>G (p.His667Arg) c.1724A>G (p.His575Arg) c.1886A>G (p.His629Arg) c.1982A>G (p.His661Arg) n.401A>G c.1943A>G (p.His648Arg) c.1775A>G (p.His592Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 21 | g.25897583T>G | CA409806256 | APP | n.2021A>C n.451A>C n.720A>C c.2054A>C (p.His685Pro) c.1829A>C (p.His610Pro) c.1661A>C (p.His554Pro) c.1997A>C (p.His666Pro) c.2000A>C (p.His667Pro) c.1724A>C (p.His575Pro) c.1886A>C (p.His629Pro) c.1982A>C (p.His661Pro) n.401A>C c.1943A>C (p.His648Pro) c.1775A>C (p.His592Pro) | |
| 21 | g.25897583T= | CA2383554906 | APP | n.2021A= n.451A= n.720A= c.2054A= (p.His685=) c.1829A= (p.His610=) c.1661A= (p.His554=) c.1997A= (p.His666=) c.2000A= (p.His667=) c.1724A= (p.His575=) c.1886A= (p.His629=) c.1982A= (p.His661=) n.401A= c.1943A= (p.His648=) c.1775A= (p.His592=) | |
| 21 | g.25897584G>A | CA409806261 | APP | n.2020C>T n.450C>T n.719C>T c.2053C>T (p.His685Tyr) c.1828C>T (p.His610Tyr) c.1660C>T (p.His554Tyr) c.1996C>T (p.His666Tyr) c.1999C>T (p.His667Tyr) c.1723C>T (p.His575Tyr) c.1885C>T (p.His629Tyr) c.1981C>T (p.His661Tyr) n.400C>T c.1942C>T (p.His648Tyr) c.1774C>T (p.His592Tyr) | |
| 21 | g.25897584G>C | CA409806262 | APP | n.2020C>G n.450C>G n.719C>G c.2053C>G (p.His685Asp) c.1828C>G (p.His610Asp) c.1660C>G (p.His554Asp) c.1996C>G (p.His666Asp) c.1999C>G (p.His667Asp) c.1723C>G (p.His575Asp) c.1885C>G (p.His629Asp) c.1981C>G (p.His661Asp) n.400C>G c.1942C>G (p.His648Asp) c.1774C>G (p.His592Asp) | |
| 21 | g.25897584G>T | CA409806264 | APP | n.2020C>A n.450C>A n.719C>A c.2053C>A (p.His685Asn) c.1828C>A (p.His610Asn) c.1660C>A (p.His554Asn) c.1996C>A (p.His666Asn) c.1999C>A (p.His667Asn) c.1723C>A (p.His575Asn) c.1885C>A (p.His629Asn) c.1981C>A (p.His661Asn) n.400C>A c.1942C>A (p.His648Asn) c.1774C>A (p.His592Asn) | |
| 21 | g.25897585A>C | CA409806266 | APP | n.2019T>G n.449T>G n.718T>G c.2052T>G (p.His684Gln) c.1827T>G (p.His609Gln) c.1659T>G (p.His553Gln) c.1995T>G (p.His665Gln) c.1998T>G (p.His666Gln) c.1722T>G (p.His574Gln) c.1884T>G (p.His628Gln) c.1980T>G (p.His660Gln) n.399T>G c.1941T>G (p.His647Gln) c.1773T>G (p.His591Gln) | |
| 21 | g.25897585A>G | CA511686146 | APP | n.2019T>C n.449T>C n.718T>C c.2052T>C (p.His684=) c.1827T>C (p.His609=) c.1659T>C (p.His553=) c.1995T>C (p.His665=) c.1998T>C (p.His666=) c.1722T>C (p.His574=) c.1884T>C (p.His628=) c.1980T>C (p.His660=) n.399T>C c.1941T>C (p.His647=) c.1773T>C (p.His591=) | |
| 21 | g.25897585A>T | CA409806268 | APP | n.2019T>A n.449T>A n.718T>A c.2052T>A (p.His684Gln) c.1827T>A (p.His609Gln) c.1659T>A (p.His553Gln) c.1995T>A (p.His665Gln) c.1998T>A (p.His666Gln) c.1722T>A (p.His574Gln) c.1884T>A (p.His628Gln) c.1980T>A (p.His660Gln) n.399T>A c.1941T>A (p.His647Gln) c.1773T>A (p.His591Gln) | COSMIC |
| 21 | g.25897586T>A | CA409806270 | APP | n.2018A>T n.448A>T n.717A>T c.2051A>T (p.His684Leu) c.1826A>T (p.His609Leu) c.1658A>T (p.His553Leu) c.1994A>T (p.His665Leu) c.1997A>T (p.His666Leu) c.1721A>T (p.His574Leu) c.1883A>T (p.His628Leu) c.1979A>T (p.His660Leu) n.398A>T c.1940A>T (p.His647Leu) c.1772A>T (p.His591Leu) | dbSNP |
| 21 | g.25897586T>C | CA409806272 | APP | n.2018A>G n.448A>G n.717A>G c.2051A>G (p.His684Arg) c.1826A>G (p.His609Arg) c.1658A>G (p.His553Arg) c.1994A>G (p.His665Arg) c.1997A>G (p.His666Arg) c.1721A>G (p.His574Arg) c.1883A>G (p.His628Arg) c.1979A>G (p.His660Arg) n.398A>G c.1940A>G (p.His647Arg) c.1772A>G (p.His591Arg) | gnomAD v4 |
| 21 | g.25897586T>G | CA409806274 | APP | n.2018A>C n.448A>C n.717A>C c.2051A>C (p.His684Pro) c.1826A>C (p.His609Pro) c.1658A>C (p.His553Pro) c.1994A>C (p.His665Pro) c.1997A>C (p.His666Pro) c.1721A>C (p.His574Pro) c.1883A>C (p.His628Pro) c.1979A>C (p.His660Pro) n.398A>C c.1940A>C (p.His647Pro) c.1772A>C (p.His591Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 21 | g.25897586T= | CA2383554907 | APP | n.2018A= n.448A= n.717A= c.2051A= (p.His684=) c.1826A= (p.His609=) c.1658A= (p.His553=) c.1994A= (p.His665=) c.1997A= (p.His666=) c.1721A= (p.His574=) c.1883A= (p.His628=) c.1979A= (p.His660=) n.398A= c.1940A= (p.His647=) c.1772A= (p.His591=) | |
| 21 | g.25897587G>A | CA409806277 | APP | n.2017C>T n.447C>T n.716C>T c.2050C>T (p.His684Tyr) c.1825C>T (p.His609Tyr) c.1657C>T (p.His553Tyr) c.1993C>T (p.His665Tyr) c.1996C>T (p.His666Tyr) c.1720C>T (p.His574Tyr) c.1882C>T (p.His628Tyr) c.1978C>T (p.His660Tyr) n.397C>T c.1939C>T (p.His647Tyr) c.1771C>T (p.His591Tyr) | gnomAD v4 |
| 21 | g.25897587G>C | CA409806278 | APP | n.2017C>G n.447C>G n.716C>G c.2050C>G (p.His684Asp) c.1825C>G (p.His609Asp) c.1657C>G (p.His553Asp) c.1993C>G (p.His665Asp) c.1996C>G (p.His666Asp) c.1720C>G (p.His574Asp) c.1882C>G (p.His628Asp) c.1978C>G (p.His660Asp) n.397C>G c.1939C>G (p.His647Asp) c.1771C>G (p.His591Asp) | |
| 21 | g.25897587G>T | CA409806280 | APP | n.2017C>A n.447C>A n.716C>A c.2050C>A (p.His684Asn) c.1825C>A (p.His609Asn) c.1657C>A (p.His553Asn) c.1993C>A (p.His665Asn) c.1996C>A (p.His666Asn) c.1720C>A (p.His574Asn) c.1882C>A (p.His628Asn) c.1978C>A (p.His660Asn) n.397C>A c.1939C>A (p.His647Asn) c.1771C>A (p.His591Asn) | |
| 21 | g.25897588A= | CA2383554908 | APP | n.2016T= n.446T= n.715T= c.2049T= (p.Val683=) c.1824T= (p.Val608=) c.1656T= (p.Val552=) c.1992T= (p.Val664=) c.1995T= (p.Val665=) c.1719T= (p.Val573=) c.1881T= (p.Val627=) c.1977T= (p.Val659=) n.396T= c.1938T= (p.Val646=) c.1770T= (p.Val590=) | |
| 21 | g.25897588A>C | CA511686150 | APP | n.2016T>G n.446T>G n.715T>G c.2049T>G (p.Val683=) c.1824T>G (p.Val608=) c.1656T>G (p.Val552=) c.1992T>G (p.Val664=) c.1995T>G (p.Val665=) c.1719T>G (p.Val573=) c.1881T>G (p.Val627=) c.1977T>G (p.Val659=) n.396T>G c.1938T>G (p.Val646=) c.1770T>G (p.Val590=) | |
| 21 | g.25897588A>G | CA511686151 | APP | n.2016T>C n.446T>C n.715T>C c.2049T>C (p.Val683=) c.1824T>C (p.Val608=) c.1656T>C (p.Val552=) c.1992T>C (p.Val664=) c.1995T>C (p.Val665=) c.1719T>C (p.Val573=) c.1881T>C (p.Val627=) c.1977T>C (p.Val659=) n.396T>C c.1938T>C (p.Val646=) c.1770T>C (p.Val590=) | |
| 21 | g.25897588A>T | CA9987088 | APP | n.2016T>A n.446T>A n.715T>A c.2049T>A (p.Val683=) c.1824T>A (p.Val608=) c.1656T>A (p.Val552=) c.1992T>A (p.Val664=) c.1995T>A (p.Val665=) c.1719T>A (p.Val573=) c.1881T>A (p.Val627=) c.1977T>A (p.Val659=) n.396T>A c.1938T>A (p.Val646=) c.1770T>A (p.Val590=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 21 | g.25897589A>C | CA409806285 | APP | n.2015T>G n.445T>G n.714T>G c.2048T>G (p.Val683Gly) c.1823T>G (p.Val608Gly) c.1655T>G (p.Val552Gly) c.1991T>G (p.Val664Gly) c.1994T>G (p.Val665Gly) c.1718T>G (p.Val573Gly) c.1880T>G (p.Val627Gly) c.1976T>G (p.Val659Gly) n.395T>G c.1937T>G (p.Val646Gly) c.1769T>G (p.Val590Gly) | |
| 21 | g.25897589A>G | CA409806287 | APP | n.2015T>C n.445T>C n.714T>C c.2048T>C (p.Val683Ala) c.1823T>C (p.Val608Ala) c.1655T>C (p.Val552Ala) c.1991T>C (p.Val664Ala) c.1994T>C (p.Val665Ala) c.1718T>C (p.Val573Ala) c.1880T>C (p.Val627Ala) c.1976T>C (p.Val659Ala) n.395T>C c.1937T>C (p.Val646Ala) c.1769T>C (p.Val590Ala) | |
| 21 | g.25897589A>T | CA409806283 | APP | n.2015T>A n.445T>A n.714T>A c.2048T>A (p.Val683Asp) c.1823T>A (p.Val608Asp) c.1655T>A (p.Val552Asp) c.1991T>A (p.Val664Asp) c.1994T>A (p.Val665Asp) c.1718T>A (p.Val573Asp) c.1880T>A (p.Val627Asp) c.1976T>A (p.Val659Asp) n.395T>A c.1937T>A (p.Val646Asp) c.1769T>A (p.Val590Asp) | |
| 21 | g.25897590C>A | CA409806291 | APP | n.2014G>T n.444G>T n.713G>T c.2047G>T (p.Val683Phe) c.1822G>T (p.Val608Phe) c.1654G>T (p.Val552Phe) c.1990G>T (p.Val664Phe) c.1993G>T (p.Val665Phe) c.1717G>T (p.Val573Phe) c.1879G>T (p.Val627Phe) c.1975G>T (p.Val659Phe) n.394G>T c.1936G>T (p.Val646Phe) c.1768G>T (p.Val590Phe) | |
| 21 | g.25897590C= | CA2383554909 | APP | n.2014G= n.444G= n.713G= c.2047G= (p.Val683=) c.1822G= (p.Val608=) c.1654G= (p.Val552=) c.1990G= (p.Val664=) c.1993G= (p.Val665=) c.1717G= (p.Val573=) c.1879G= (p.Val627=) c.1975G= (p.Val659=) n.394G= c.1936G= (p.Val646=) c.1768G= (p.Val590=) | |
| 21 | g.25897590C>G | CA409806289 | APP | n.2014G>C n.444G>C n.713G>C c.2047G>C (p.Val683Leu) c.1822G>C (p.Val608Leu) c.1654G>C (p.Val552Leu) c.1990G>C (p.Val664Leu) c.1993G>C (p.Val665Leu) c.1717G>C (p.Val573Leu) c.1879G>C (p.Val627Leu) c.1975G>C (p.Val659Leu) n.394G>C c.1936G>C (p.Val646Leu) c.1768G>C (p.Val590Leu) | |
| 21 | g.25897590C>T | CA9987089 | APP | n.2014G>A n.444G>A n.713G>A c.2047G>A (p.Val683Ile) c.1822G>A (p.Val608Ile) c.1654G>A (p.Val552Ile) c.1990G>A (p.Val664Ile) c.1993G>A (p.Val665Ile) c.1717G>A (p.Val573Ile) c.1879G>A (p.Val627Ile) c.1975G>A (p.Val659Ile) n.394G>A c.1936G>A (p.Val646Ile) c.1768G>A (p.Val590Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 21 | g.25897591T>A | CA409806294 | APP | n.2013A>T n.443A>T n.712A>T c.2046A>T (p.Glu682Asp) c.1821A>T (p.Glu607Asp) c.1653A>T (p.Glu551Asp) c.1989A>T (p.Glu663Asp) c.1992A>T (p.Glu664Asp) c.1716A>T (p.Glu572Asp) c.1878A>T (p.Glu626Asp) c.1974A>T (p.Glu658Asp) n.393A>T c.1935A>T (p.Glu645Asp) c.1767A>T (p.Glu589Asp) | |
| 21 | g.25897591T>C | CA511686155 | APP | n.2013A>G n.443A>G n.712A>G c.2046A>G (p.Glu682=) c.1821A>G (p.Glu607=) c.1653A>G (p.Glu551=) c.1989A>G (p.Glu663=) c.1992A>G (p.Glu664=) c.1716A>G (p.Glu572=) c.1878A>G (p.Glu626=) c.1974A>G (p.Glu658=) n.393A>G c.1935A>G (p.Glu645=) c.1767A>G (p.Glu589=) | ClinVar dbSNP gnomAD v4 |
| 21 | g.25897591T>G | CA409806296 | APP | n.2013A>C n.443A>C n.712A>C c.2046A>C (p.Glu682Asp) c.1821A>C (p.Glu607Asp) c.1653A>C (p.Glu551Asp) c.1989A>C (p.Glu663Asp) c.1992A>C (p.Glu664Asp) c.1716A>C (p.Glu572Asp) c.1878A>C (p.Glu626Asp) c.1974A>C (p.Glu658Asp) n.393A>C c.1935A>C (p.Glu645Asp) c.1767A>C (p.Glu589Asp) | |
| 21 | g.25897591T= | CA2383554910 | APP | n.2013A= n.443A= n.712A= c.2046A= (p.Glu682=) c.1821A= (p.Glu607=) c.1653A= (p.Glu551=) c.1989A= (p.Glu663=) c.1992A= (p.Glu664=) c.1716A= (p.Glu572=) c.1878A= (p.Glu626=) c.1974A= (p.Glu658=) n.393A= c.1935A= (p.Glu645=) c.1767A= (p.Glu589=) | |
| 21 | g.25897592T>A | CA409806298 | APP | n.2012A>T n.442A>T n.711A>T c.2045A>T (p.Glu682Val) c.1820A>T (p.Glu607Val) c.1652A>T (p.Glu551Val) c.1988A>T (p.Glu663Val) c.1991A>T (p.Glu664Val) c.1715A>T (p.Glu572Val) c.1877A>T (p.Glu626Val) c.1973A>T (p.Glu658Val) n.392A>T c.1934A>T (p.Glu645Val) c.1766A>T (p.Glu589Val) | |
| 21 | g.25897592T>C | CA409806300 | APP | n.2012A>G n.442A>G n.711A>G c.2045A>G (p.Glu682Gly) c.1820A>G (p.Glu607Gly) c.1652A>G (p.Glu551Gly) c.1988A>G (p.Glu663Gly) c.1991A>G (p.Glu664Gly) c.1715A>G (p.Glu572Gly) c.1877A>G (p.Glu626Gly) c.1973A>G (p.Glu658Gly) n.392A>G c.1934A>G (p.Glu645Gly) c.1766A>G (p.Glu589Gly) |