Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.25891776G>A | CA511685987 | APP | n.2124C>T n.554C>T n.823C>T c.2157C>T (p.Thr719=) c.1932C>T (p.Thr644=) c.1764C>T (p.Thr588=) c.2100C>T (p.Thr700=) c.2103C>T (p.Thr701=) c.1827C>T (p.Thr609=) c.1989C>T (p.Thr663=) c.2085C>T (p.Thr695=) n.504C>T c.2046C>T (p.Thr682=) c.1878C>T (p.Thr626=) | gnomAD v4 |
21 | g.25891776G>C | CA511685988 | APP | n.2124C>G n.554C>G n.823C>G c.2157C>G (p.Thr719=) c.1932C>G (p.Thr644=) c.1764C>G (p.Thr588=) c.2100C>G (p.Thr700=) c.2103C>G (p.Thr701=) c.1827C>G (p.Thr609=) c.1989C>G (p.Thr663=) c.2085C>G (p.Thr695=) n.504C>G c.2046C>G (p.Thr682=) c.1878C>G (p.Thr626=) | |
21 | g.25891776G>T | CA511685989 | APP | n.2124C>A n.554C>A n.823C>A c.2157C>A (p.Thr719=) c.1932C>A (p.Thr644=) c.1764C>A (p.Thr588=) c.2100C>A (p.Thr700=) c.2103C>A (p.Thr701=) c.1827C>A (p.Thr609=) c.1989C>A (p.Thr663=) c.2085C>A (p.Thr695=) n.504C>A c.2046C>A (p.Thr682=) c.1878C>A (p.Thr626=) | |
21 | g.25891777G>A | CA409805537 | APP | n.2123C>T n.553C>T n.822C>T c.2156C>T (p.Thr719Ile) c.1931C>T (p.Thr644Ile) c.1763C>T (p.Thr588Ile) c.2099C>T (p.Thr700Ile) c.2102C>T (p.Thr701Ile) c.1826C>T (p.Thr609Ile) c.1988C>T (p.Thr663Ile) c.2084C>T (p.Thr695Ile) n.503C>T c.2045C>T (p.Thr682Ile) c.1877C>T (p.Thr626Ile) | dbSNP |
21 | g.25891777G>C | CA409805538 | APP | n.2123C>G n.553C>G n.822C>G c.2156C>G (p.Thr719Ser) c.1931C>G (p.Thr644Ser) c.1763C>G (p.Thr588Ser) c.2099C>G (p.Thr700Ser) c.2102C>G (p.Thr701Ser) c.1826C>G (p.Thr609Ser) c.1988C>G (p.Thr663Ser) c.2084C>G (p.Thr695Ser) n.503C>G c.2045C>G (p.Thr682Ser) c.1877C>G (p.Thr626Ser) | |
21 | g.25891777G= | CA2383551607 | APP | n.2123C= n.553C= n.822C= c.2156C= (p.Thr719=) c.1931C= (p.Thr644=) c.1763C= (p.Thr588=) c.2099C= (p.Thr700=) c.2102C= (p.Thr701=) c.1826C= (p.Thr609=) c.1988C= (p.Thr663=) c.2084C= (p.Thr695=) n.503C= c.2045C= (p.Thr682=) c.1877C= (p.Thr626=) | |
21 | g.25891777G>T | CA409805539 | APP | n.2123C>A n.553C>A n.822C>A c.2156C>A (p.Thr719Asn) c.1931C>A (p.Thr644Asn) c.1763C>A (p.Thr588Asn) c.2099C>A (p.Thr700Asn) c.2102C>A (p.Thr701Asn) c.1826C>A (p.Thr609Asn) c.1988C>A (p.Thr663Asn) c.2084C>A (p.Thr695Asn) n.503C>A c.2045C>A (p.Thr682Asn) c.1877C>A (p.Thr626Asn) | |
21 | g.25891778T>A | CA409805540 | APP | n.2122A>T n.552A>T n.821A>T c.2155A>T (p.Thr719Ser) c.1930A>T (p.Thr644Ser) c.1762A>T (p.Thr588Ser) c.2098A>T (p.Thr700Ser) c.2101A>T (p.Thr701Ser) c.1825A>T (p.Thr609Ser) c.1987A>T (p.Thr663Ser) c.2083A>T (p.Thr695Ser) n.502A>T c.2044A>T (p.Thr682Ser) c.1876A>T (p.Thr626Ser) | |
21 | g.25891778T>C | CA409805541 | APP | n.2122A>G n.552A>G n.821A>G c.2155A>G (p.Thr719Ala) c.1930A>G (p.Thr644Ala) c.1762A>G (p.Thr588Ala) c.2098A>G (p.Thr700Ala) c.2101A>G (p.Thr701Ala) c.1825A>G (p.Thr609Ala) c.1987A>G (p.Thr663Ala) c.2083A>G (p.Thr695Ala) n.502A>G c.2044A>G (p.Thr682Ala) c.1876A>G (p.Thr626Ala) | |
21 | g.25891778T>G | CA409805542 | APP | n.2122A>C n.552A>C n.821A>C c.2155A>C (p.Thr719Pro) c.1930A>C (p.Thr644Pro) c.1762A>C (p.Thr588Pro) c.2098A>C (p.Thr700Pro) c.2101A>C (p.Thr701Pro) c.1825A>C (p.Thr609Pro) c.1987A>C (p.Thr663Pro) c.2083A>C (p.Thr695Pro) n.502A>C c.2044A>C (p.Thr682Pro) c.1876A>C (p.Thr626Pro) | ClinVar dbSNP |
21 | g.25891779G>A | CA511685992 | APP | n.2121C>T n.551C>T n.820C>T c.2154C>T (p.Ile718=) c.1929C>T (p.Ile643=) c.1761C>T (p.Ile587=) c.2097C>T (p.Ile699=) c.2100C>T (p.Ile700=) c.1824C>T (p.Ile608=) c.1986C>T (p.Ile662=) c.2082C>T (p.Ile694=) n.501C>T c.2043C>T (p.Ile681=) c.1875C>T (p.Ile625=) | |
21 | g.25891779G>C | CA409805543 | APP | n.2121C>G n.551C>G n.820C>G c.2154C>G (p.Ile718Met) c.1929C>G (p.Ile643Met) c.1761C>G (p.Ile587Met) c.2097C>G (p.Ile699Met) c.2100C>G (p.Ile700Met) c.1824C>G (p.Ile608Met) c.1986C>G (p.Ile662Met) c.2082C>G (p.Ile694Met) n.501C>G c.2043C>G (p.Ile681Met) c.1875C>G (p.Ile625Met) | |
21 | g.25891779G>T | CA511685991 | APP | n.2121C>A n.551C>A n.820C>A c.2154C>A (p.Ile718=) c.1929C>A (p.Ile643=) c.1761C>A (p.Ile587=) c.2097C>A (p.Ile699=) c.2100C>A (p.Ile700=) c.1824C>A (p.Ile608=) c.1986C>A (p.Ile662=) c.2082C>A (p.Ile694=) n.501C>A c.2043C>A (p.Ile681=) c.1875C>A (p.Ile625=) | |
21 | g.25891780A>C | CA409805544 | APP | n.2120T>G n.550T>G n.819T>G c.2153T>G (p.Ile718Ser) c.1928T>G (p.Ile643Ser) c.1760T>G (p.Ile587Ser) c.2096T>G (p.Ile699Ser) c.2099T>G (p.Ile700Ser) c.1823T>G (p.Ile608Ser) c.1985T>G (p.Ile662Ser) c.2081T>G (p.Ile694Ser) n.500T>G c.2042T>G (p.Ile681Ser) c.1874T>G (p.Ile625Ser) | |
21 | g.25891780A>G | CA409805545 | APP | n.2120T>C n.550T>C n.819T>C c.2153T>C (p.Ile718Thr) c.1928T>C (p.Ile643Thr) c.1760T>C (p.Ile587Thr) c.2096T>C (p.Ile699Thr) c.2099T>C (p.Ile700Thr) c.1823T>C (p.Ile608Thr) c.1985T>C (p.Ile662Thr) c.2081T>C (p.Ile694Thr) n.500T>C c.2042T>C (p.Ile681Thr) c.1874T>C (p.Ile625Thr) | |
21 | g.25891780A>T | CA409805546 | APP | n.2120T>A n.550T>A n.819T>A c.2153T>A (p.Ile718Asn) c.1928T>A (p.Ile643Asn) c.1760T>A (p.Ile587Asn) c.2096T>A (p.Ile699Asn) c.2099T>A (p.Ile700Asn) c.1823T>A (p.Ile608Asn) c.1985T>A (p.Ile662Asn) c.2081T>A (p.Ile694Asn) n.500T>A c.2042T>A (p.Ile681Asn) c.1874T>A (p.Ile625Asn) | |
21 | g.25891781T>A | CA409805548 | APP | n.2119A>T n.549A>T n.818A>T c.2152A>T (p.Ile718Phe) c.1927A>T (p.Ile643Phe) c.1759A>T (p.Ile587Phe) c.2095A>T (p.Ile699Phe) c.2098A>T (p.Ile700Phe) c.1822A>T (p.Ile608Phe) c.1984A>T (p.Ile662Phe) c.2080A>T (p.Ile694Phe) n.499A>T c.2041A>T (p.Ile681Phe) c.1873A>T (p.Ile625Phe) | dbSNP gnomAD v2 gnomAD v4 |
21 | g.25891781T>C | CA409805549 | APP | n.2119A>G n.549A>G n.818A>G c.2152A>G (p.Ile718Val) c.1927A>G (p.Ile643Val) c.1759A>G (p.Ile587Val) c.2095A>G (p.Ile699Val) c.2098A>G (p.Ile700Val) c.1822A>G (p.Ile608Val) c.1984A>G (p.Ile662Val) c.2080A>G (p.Ile694Val) n.499A>G c.2041A>G (p.Ile681Val) c.1873A>G (p.Ile625Val) | dbSNP gnomAD v4 |
21 | g.25891781T>G | CA409805547 | APP | n.2119A>C n.549A>C n.818A>C c.2152A>C (p.Ile718Leu) c.1927A>C (p.Ile643Leu) c.1759A>C (p.Ile587Leu) c.2095A>C (p.Ile699Leu) c.2098A>C (p.Ile700Leu) c.1822A>C (p.Ile608Leu) c.1984A>C (p.Ile662Leu) c.2080A>C (p.Ile694Leu) n.499A>C c.2041A>C (p.Ile681Leu) c.1873A>C (p.Ile625Leu) | |
21 | g.25891781T= | CA2383551608 | APP | n.2119A= n.549A= n.818A= c.2152A= (p.Ile718=) c.1927A= (p.Ile643=) c.1759A= (p.Ile587=) c.2095A= (p.Ile699=) c.2098A= (p.Ile700=) c.1822A= (p.Ile608=) c.1984A= (p.Ile662=) c.2080A= (p.Ile694=) n.499A= c.2041A= (p.Ile681=) c.1873A= (p.Ile625=) | |
21 | g.25891782_25891783insCTG | CA2830561775 | APP | n.2119_2120insGCA n.549_550insGCA n.818_819insGCA c.2152_2153insGCA (p.Val717_Ile718insSer) c.1927_1928insGCA (p.Val642_Ile643insSer) c.1759_1760insGCA (p.Val586_Ile587insSer) c.2095_2096insGCA (p.Val698_Ile699insSer) c.2098_2099insGCA (p.Val699_Ile700insSer) c.1822_1823insGCA (p.Val607_Ile608insSer) c.1984_1985insGCA (p.Val661_Ile662insSer) c.2080_2081insGCA (p.Val693_Ile694insSer) n.499_500insGCA c.2041_2042insGCA (p.Val680_Ile681insSer) c.1873_1874insGCA (p.Val624_Ile625insSer) | |
21 | g.25891782G>A | CA511685995 | APP | n.2118C>T n.548C>T n.817C>T c.2151C>T (p.Val717=) c.1926C>T (p.Val642=) c.1758C>T (p.Val586=) c.2094C>T (p.Val698=) c.2097C>T (p.Val699=) c.1821C>T (p.Val607=) c.1983C>T (p.Val661=) c.2079C>T (p.Val693=) n.498C>T c.2040C>T (p.Val680=) c.1872C>T (p.Val624=) | |
21 | g.25891782G>C | CA511685993 | APP | n.2118C>G n.548C>G n.817C>G c.2151C>G (p.Val717=) c.1926C>G (p.Val642=) c.1758C>G (p.Val586=) c.2094C>G (p.Val698=) c.2097C>G (p.Val699=) c.1821C>G (p.Val607=) c.1983C>G (p.Val661=) c.2079C>G (p.Val693=) n.498C>G c.2040C>G (p.Val680=) c.1872C>G (p.Val624=) | |
21 | g.25891782G= | CA2383551609 | APP | n.2118C= n.548C= n.817C= c.2151C= (p.Val717=) c.1926C= (p.Val642=) c.1758C= (p.Val586=) c.2094C= (p.Val698=) c.2097C= (p.Val699=) c.1821C= (p.Val607=) c.1983C= (p.Val661=) c.2079C= (p.Val693=) n.498C= c.2040C= (p.Val680=) c.1872C= (p.Val624=) | |
21 | g.25891782G>T | CA511685994 | APP | n.2118C>A n.548C>A n.817C>A c.2151C>A (p.Val717=) c.1926C>A (p.Val642=) c.1758C>A (p.Val586=) c.2094C>A (p.Val698=) c.2097C>A (p.Val699=) c.1821C>A (p.Val607=) c.1983C>A (p.Val661=) c.2079C>A (p.Val693=) n.498C>A c.2040C>A (p.Val680=) c.1872C>A (p.Val624=) | dbSNP gnomAD v4 |
21 | g.25891784_25891786del | CA2817564437 | APP | n.2116_2118del n.546_548del n.815_817del c.2149_2151del (p.Val717del) c.1924_1926del (p.Val642del) c.1756_1758del (p.Val586del) c.2092_2094del (p.Val698del) c.2095_2097del (p.Val699del) c.1819_1821del (p.Val607del) c.1981_1983del (p.Val661del) c.2077_2079del (p.Val693del) n.496_498del c.2038_2040del (p.Val680del) c.1870_1872del (p.Val624del) | |
21 | g.25891783A= | CA2383551610 | APP | n.2117T= n.547T= n.816T= c.2150T= (p.Val717=) c.1925T= (p.Val642=) c.1757T= (p.Val586=) c.2093T= (p.Val698=) c.2096T= (p.Val699=) c.1820T= (p.Val607=) c.1982T= (p.Val661=) c.2078T= (p.Val693=) n.497T= c.2039T= (p.Val680=) c.1871T= (p.Val624=) | |
21 | g.25891783A>C | CA127793 | APP | n.2117T>G n.547T>G n.816T>G c.2150T>G (p.Val717Gly) c.1925T>G (p.Val642Gly) c.1757T>G (p.Val586Gly) c.2093T>G (p.Val698Gly) c.2096T>G (p.Val699Gly) c.1820T>G (p.Val607Gly) c.1982T>G (p.Val661Gly) c.2078T>G (p.Val693Gly) n.497T>G c.2039T>G (p.Val680Gly) c.1871T>G (p.Val624Gly) | ClinVar dbSNP |
21 | g.25891783A>G | CA409805550 | APP | n.2117T>C n.547T>C n.816T>C c.2150T>C (p.Val717Ala) c.1925T>C (p.Val642Ala) c.1757T>C (p.Val586Ala) c.2093T>C (p.Val698Ala) c.2096T>C (p.Val699Ala) c.1820T>C (p.Val607Ala) c.1982T>C (p.Val661Ala) c.2078T>C (p.Val693Ala) n.497T>C c.2039T>C (p.Val680Ala) c.1871T>C (p.Val624Ala) | |
21 | g.25891783A>T | CA409805551 | APP | n.2117T>A n.547T>A n.816T>A c.2150T>A (p.Val717Asp) c.1925T>A (p.Val642Asp) c.1757T>A (p.Val586Asp) c.2093T>A (p.Val698Asp) c.2096T>A (p.Val699Asp) c.1820T>A (p.Val607Asp) c.1982T>A (p.Val661Asp) c.2078T>A (p.Val693Asp) n.497T>A c.2039T>A (p.Val680Asp) c.1871T>A (p.Val624Asp) | |
21 | g.25891784C>A | CA127792 | APP | n.2116G>T n.546G>T n.815G>T c.2149G>T (p.Val717Phe) c.1924G>T (p.Val642Phe) c.1756G>T (p.Val586Phe) c.2092G>T (p.Val698Phe) c.2095G>T (p.Val699Phe) c.1819G>T (p.Val607Phe) c.1981G>T (p.Val661Phe) c.2077G>T (p.Val693Phe) n.496G>T c.2038G>T (p.Val680Phe) c.1870G>T (p.Val624Phe) | ClinVar dbSNP |
21 | g.25891784C= | CA2383551611 | APP | n.2116G= n.546G= n.815G= c.2149G= (p.Val717=) c.1924G= (p.Val642=) c.1756G= (p.Val586=) c.2092G= (p.Val698=) c.2095G= (p.Val699=) c.1819G= (p.Val607=) c.1981G= (p.Val661=) c.2077G= (p.Val693=) n.496G= c.2038G= (p.Val680=) c.1870G= (p.Val624=) | |
21 | g.25891784C>G | CA127816 | APP | n.2116G>C n.546G>C n.815G>C c.2149G>C (p.Val717Leu) c.1924G>C (p.Val642Leu) c.1756G>C (p.Val586Leu) c.2092G>C (p.Val698Leu) c.2095G>C (p.Val699Leu) c.1819G>C (p.Val607Leu) c.1981G>C (p.Val661Leu) c.2077G>C (p.Val693Leu) n.496G>C c.2038G>C (p.Val680Leu) c.1870G>C (p.Val624Leu) | ClinVar dbSNP |
21 | g.25891784C>T | CA127791 | APP | n.2116G>A n.546G>A n.815G>A c.2149G>A (p.Val717Ile) c.1924G>A (p.Val642Ile) c.1756G>A (p.Val586Ile) c.2092G>A (p.Val698Ile) c.2095G>A (p.Val699Ile) c.1819G>A (p.Val607Ile) c.1981G>A (p.Val661Ile) c.2077G>A (p.Val693Ile) n.496G>A c.2038G>A (p.Val680Ile) c.1870G>A (p.Val624Ile) | ClinVar dbSNP gnomAD v4 |
21 | g.25891785G>A | CA9987050 | APP | n.2115C>T n.545C>T n.814C>T c.2148C>T (p.Ile716=) c.1923C>T (p.Ile641=) c.1755C>T (p.Ile585=) c.2091C>T (p.Ile697=) c.2094C>T (p.Ile698=) c.1818C>T (p.Ile606=) c.1980C>T (p.Ile660=) c.2076C>T (p.Ile692=) n.495C>T c.2037C>T (p.Ile679=) c.1869C>T (p.Ile623=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
21 | g.25891785G>C | CA409805552 | APP | n.2115C>G n.545C>G n.814C>G c.2148C>G (p.Ile716Met) c.1923C>G (p.Ile641Met) c.1755C>G (p.Ile585Met) c.2091C>G (p.Ile697Met) c.2094C>G (p.Ile698Met) c.1818C>G (p.Ile606Met) c.1980C>G (p.Ile660Met) c.2076C>G (p.Ile692Met) n.495C>G c.2037C>G (p.Ile679Met) c.1869C>G (p.Ile623Met) | ClinVar dbSNP gnomAD v4 |
21 | g.25891785G= | CA2383551612 | APP | n.2115C= n.545C= n.814C= c.2148C= (p.Ile716=) c.1923C= (p.Ile641=) c.1755C= (p.Ile585=) c.2091C= (p.Ile697=) c.2094C= (p.Ile698=) c.1818C= (p.Ile606=) c.1980C= (p.Ile660=) c.2076C= (p.Ile692=) n.495C= c.2037C= (p.Ile679=) c.1869C= (p.Ile623=) | |
21 | g.25891785G>T | CA9987049 | APP | n.2115C>A n.545C>A n.814C>A c.2148C>A (p.Ile716=) c.1923C>A (p.Ile641=) c.1755C>A (p.Ile585=) c.2091C>A (p.Ile697=) c.2094C>A (p.Ile698=) c.1818C>A (p.Ile606=) c.1980C>A (p.Ile660=) c.2076C>A (p.Ile692=) n.495C>A c.2037C>A (p.Ile679=) c.1869C>A (p.Ile623=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
21 | g.25891786A= | CA2383551613 | APP | n.2114T= n.544T= n.813T= c.2147T= (p.Ile716=) c.1922T= (p.Ile641=) c.1754T= (p.Ile585=) c.2090T= (p.Ile697=) c.2093T= (p.Ile698=) c.1817T= (p.Ile606=) c.1979T= (p.Ile660=) c.2075T= (p.Ile692=) n.494T= c.2036T= (p.Ile679=) c.1868T= (p.Ile623=) | |
21 | g.25891786A>C | CA409805553 | APP | n.2114T>G n.544T>G n.813T>G c.2147T>G (p.Ile716Ser) c.1922T>G (p.Ile641Ser) c.1754T>G (p.Ile585Ser) c.2090T>G (p.Ile697Ser) c.2093T>G (p.Ile698Ser) c.1817T>G (p.Ile606Ser) c.1979T>G (p.Ile660Ser) c.2075T>G (p.Ile692Ser) n.494T>G c.2036T>G (p.Ile679Ser) c.1868T>G (p.Ile623Ser) | |
21 | g.25891786A>G | CA225511 | APP | n.2114T>C n.544T>C n.813T>C c.2147T>C (p.Ile716Thr) c.1922T>C (p.Ile641Thr) c.1754T>C (p.Ile585Thr) c.2090T>C (p.Ile697Thr) c.2093T>C (p.Ile698Thr) c.1817T>C (p.Ile606Thr) c.1979T>C (p.Ile660Thr) c.2075T>C (p.Ile692Thr) n.494T>C c.2036T>C (p.Ile679Thr) c.1868T>C (p.Ile623Thr) | ClinVar dbSNP |
21 | g.25891786A>T | CA409805554 | APP | n.2114T>A n.544T>A n.813T>A c.2147T>A (p.Ile716Asn) c.1922T>A (p.Ile641Asn) c.1754T>A (p.Ile585Asn) c.2090T>A (p.Ile697Asn) c.2093T>A (p.Ile698Asn) c.1817T>A (p.Ile606Asn) c.1979T>A (p.Ile660Asn) c.2075T>A (p.Ile692Asn) n.494T>A c.2036T>A (p.Ile679Asn) c.1868T>A (p.Ile623Asn) | |
21 | g.25891787T>A | CA409805555 | APP | n.2113A>T n.543A>T n.812A>T c.2146A>T (p.Ile716Phe) c.1921A>T (p.Ile641Phe) c.1753A>T (p.Ile585Phe) c.2089A>T (p.Ile697Phe) c.2092A>T (p.Ile698Phe) c.1816A>T (p.Ile606Phe) c.1978A>T (p.Ile660Phe) c.2074A>T (p.Ile692Phe) n.493A>T c.2035A>T (p.Ile679Phe) c.1867A>T (p.Ile623Phe) | ClinVar dbSNP |
21 | g.25891787T>C | CA127799 | APP | n.2113A>G n.543A>G n.812A>G c.2146A>G (p.Ile716Val) c.1921A>G (p.Ile641Val) c.1753A>G (p.Ile585Val) c.2089A>G (p.Ile697Val) c.2092A>G (p.Ile698Val) c.1816A>G (p.Ile606Val) c.1978A>G (p.Ile660Val) c.2074A>G (p.Ile692Val) n.493A>G c.2035A>G (p.Ile679Val) c.1867A>G (p.Ile623Val) | ClinVar dbSNP |
21 | g.25891787T>G | CA409805556 | APP | n.2113A>C n.543A>C n.812A>C c.2146A>C (p.Ile716Leu) c.1921A>C (p.Ile641Leu) c.1753A>C (p.Ile585Leu) c.2089A>C (p.Ile697Leu) c.2092A>C (p.Ile698Leu) c.1816A>C (p.Ile606Leu) c.1978A>C (p.Ile660Leu) c.2074A>C (p.Ile692Leu) n.493A>C c.2035A>C (p.Ile679Leu) c.1867A>C (p.Ile623Leu) | |
21 | g.25891787T= | CA2383551614 | APP | n.2113A= n.543A= n.812A= c.2146A= (p.Ile716=) c.1921A= (p.Ile641=) c.1753A= (p.Ile585=) c.2089A= (p.Ile697=) c.2092A= (p.Ile698=) c.1816A= (p.Ile606=) c.1978A= (p.Ile660=) c.2074A= (p.Ile692=) n.493A= c.2035A= (p.Ile679=) c.1867A= (p.Ile623=) | |
21 | g.25891787_25891788delinsCA | CA2573157339 | APP | n.2112_2113delinsTG n.542_543delinsTG n.811_812delinsTG c.2145_2146delinsTG (p.Ile716Val) c.1920_1921delinsTG (p.Ile641Val) c.1752_1753delinsTG (p.Ile585Val) c.2088_2089delinsTG (p.Ile697Val) c.2091_2092delinsTG (p.Ile698Val) c.1815_1816delinsTG (p.Ile606Val) c.1977_1978delinsTG (p.Ile660Val) c.2073_2074delinsTG (p.Ile692Val) n.492_493delinsTG c.2034_2035delinsTG (p.Ile679Val) c.1866_1867delinsTG (p.Ile623Val) | ClinVar dbSNP |
21 | g.25891788C>A | CA511685997 | APP | n.2112G>T n.542G>T n.811G>T c.2145G>T (p.Val715=) c.1920G>T (p.Val640=) c.1752G>T (p.Val584=) c.2088G>T (p.Val696=) c.2091G>T (p.Val697=) c.1815G>T (p.Val605=) c.1977G>T (p.Val659=) c.2073G>T (p.Val691=) n.492G>T c.2034G>T (p.Val678=) c.1866G>T (p.Val622=) | |
21 | g.25891788C= | CA2383551615 | APP | n.2112G= n.542G= n.811G= c.2145G= (p.Val715=) c.1920G= (p.Val640=) c.1752G= (p.Val584=) c.2088G= (p.Val696=) c.2091G= (p.Val697=) c.1815G= (p.Val605=) c.1977G= (p.Val659=) c.2073G= (p.Val691=) n.492G= c.2034G= (p.Val678=) c.1866G= (p.Val622=) | |
21 | g.25891788C>G | CA511685996 | APP | n.2112G>C n.542G>C n.811G>C c.2145G>C (p.Val715=) c.1920G>C (p.Val640=) c.1752G>C (p.Val584=) c.2088G>C (p.Val696=) c.2091G>C (p.Val697=) c.1815G>C (p.Val605=) c.1977G>C (p.Val659=) c.2073G>C (p.Val691=) n.492G>C c.2034G>C (p.Val678=) c.1866G>C (p.Val622=) |