Chr Mutation (hg38) CAid Gene Transcript Linkouts
21g.25891786A=CA2383551613APPn.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=)
21g.25891786A>CCA409805553APPn.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)
21g.25891786A>GCA225511APPn.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
21g.25891786A>TCA409805554APPn.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)
21g.25891787T>ACA409805555APPn.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
21g.25891787T>CCA127799APPn.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
21g.25891787T>GCA409805556APPn.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)
21g.25891787T=CA2383551614APPn.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=)
21g.25891787_25891788delinsCACA2573157339APPn.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
21g.25891788C>ACA511685997APPn.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=)
21g.25891788C=CA2383551615APPn.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=)
21g.25891788C>GCA511685996APPn.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=)
21g.25891788C>TCA225509APPn.2112G>A
n.542G>A
n.811G>A
c.2145G>A (p.Val715=)
c.1920G>A (p.Val640=)
c.1752G>A (p.Val584=)
c.2088G>A (p.Val696=)
c.2091G>A (p.Val697=)
c.1815G>A (p.Val605=)
c.1977G>A (p.Val659=)
c.2073G>A (p.Val691=)
n.492G>A
c.2034G>A (p.Val678=)
c.1866G>A (p.Val622=)
ClinVar dbSNP
21g.25891789A=CA2383551616APPn.2111T=
n.541T=
n.810T=
c.2144T= (p.Val715=)
c.1919T= (p.Val640=)
c.1751T= (p.Val584=)
c.2087T= (p.Val696=)
c.2090T= (p.Val697=)
c.1814T= (p.Val605=)
c.1976T= (p.Val659=)
c.2072T= (p.Val691=)
n.491T=
c.2033T= (p.Val678=)
c.1865T= (p.Val622=)
21g.25891789A>CCA409805557APPn.2111T>G
n.541T>G
n.810T>G
c.2144T>G (p.Val715Gly)
c.1919T>G (p.Val640Gly)
c.1751T>G (p.Val584Gly)
c.2087T>G (p.Val696Gly)
c.2090T>G (p.Val697Gly)
c.1814T>G (p.Val605Gly)
c.1976T>G (p.Val659Gly)
c.2072T>G (p.Val691Gly)
n.491T>G
c.2033T>G (p.Val678Gly)
c.1865T>G (p.Val622Gly)
dbSNP gnomAD v2 gnomAD v4
21g.25891789A>GCA225507APPn.2111T>C
n.541T>C
n.810T>C
c.2144T>C (p.Val715Ala)
c.1919T>C (p.Val640Ala)
c.1751T>C (p.Val584Ala)
c.2087T>C (p.Val696Ala)
c.2090T>C (p.Val697Ala)
c.1814T>C (p.Val605Ala)
c.1976T>C (p.Val659Ala)
c.2072T>C (p.Val691Ala)
n.491T>C
c.2033T>C (p.Val678Ala)
c.1865T>C (p.Val622Ala)
ClinVar dbSNP
21g.25891789A>TCA409805558APPn.2111T>A
n.541T>A
n.810T>A
c.2144T>A (p.Val715Glu)
c.1919T>A (p.Val640Glu)
c.1751T>A (p.Val584Glu)
c.2087T>A (p.Val696Glu)
c.2090T>A (p.Val697Glu)
c.1814T>A (p.Val605Glu)
c.1976T>A (p.Val659Glu)
c.2072T>A (p.Val691Glu)
n.491T>A
c.2033T>A (p.Val678Glu)
c.1865T>A (p.Val622Glu)
21g.25891790C>ACA409805559APPn.2110G>T
n.540G>T
n.809G>T
c.2143G>T (p.Val715Leu)
c.1918G>T (p.Val640Leu)
c.1750G>T (p.Val584Leu)
c.2086G>T (p.Val696Leu)
c.2089G>T (p.Val697Leu)
c.1813G>T (p.Val605Leu)
c.1975G>T (p.Val659Leu)
c.2071G>T (p.Val691Leu)
n.490G>T
c.2032G>T (p.Val678Leu)
c.1864G>T (p.Val622Leu)
21g.25891790C=CA2383551617APPn.2110G=
n.540G=
n.809G=
c.2143G= (p.Val715=)
c.1918G= (p.Val640=)
c.1750G= (p.Val584=)
c.2086G= (p.Val696=)
c.2089G= (p.Val697=)
c.1813G= (p.Val605=)
c.1975G= (p.Val659=)
c.2071G= (p.Val691=)
n.490G=
c.2032G= (p.Val678=)
c.1864G= (p.Val622=)
21g.25891790C>GCA409805560APPn.2110G>C
n.540G>C
n.809G>C
c.2143G>C (p.Val715Leu)
c.1918G>C (p.Val640Leu)
c.1750G>C (p.Val584Leu)
c.2086G>C (p.Val696Leu)
c.2089G>C (p.Val697Leu)
c.1813G>C (p.Val605Leu)
c.1975G>C (p.Val659Leu)
c.2071G>C (p.Val691Leu)
n.490G>C
c.2032G>C (p.Val678Leu)
c.1864G>C (p.Val622Leu)
21g.25891790C>TCA127800APPn.2110G>A
n.540G>A
n.809G>A
c.2143G>A (p.Val715Met)
c.1918G>A (p.Val640Met)
c.1750G>A (p.Val584Met)
c.2086G>A (p.Val696Met)
c.2089G>A (p.Val697Met)
c.1813G>A (p.Val605Met)
c.1975G>A (p.Val659Met)
c.2071G>A (p.Val691Met)
n.490G>A
c.2032G>A (p.Val678Met)
c.1864G>A (p.Val622Met)
ClinVar dbSNP
21g.25891791T>ACA511685999APPn.2109A>T
n.539A>T
n.808A>T
c.2142A>T (p.Thr714=)
c.1917A>T (p.Thr639=)
c.1749A>T (p.Thr583=)
c.2085A>T (p.Thr695=)
c.2088A>T (p.Thr696=)
c.1812A>T (p.Thr604=)
c.1974A>T (p.Thr658=)
c.2070A>T (p.Thr690=)
n.489A>T
c.2031A>T (p.Thr677=)
c.1863A>T (p.Thr621=)
21g.25891791T>CCA511686001APPn.2109A>G
n.539A>G
n.808A>G
c.2142A>G (p.Thr714=)
c.1917A>G (p.Thr639=)
c.1749A>G (p.Thr583=)
c.2085A>G (p.Thr695=)
c.2088A>G (p.Thr696=)
c.1812A>G (p.Thr604=)
c.1974A>G (p.Thr658=)
c.2070A>G (p.Thr690=)
n.489A>G
c.2031A>G (p.Thr677=)
c.1863A>G (p.Thr621=)
gnomAD v4
21g.25891791T>GCA511686000APPn.2109A>C
n.539A>C
n.808A>C
c.2142A>C (p.Thr714=)
c.1917A>C (p.Thr639=)
c.1749A>C (p.Thr583=)
c.2085A>C (p.Thr695=)
c.2088A>C (p.Thr696=)
c.1812A>C (p.Thr604=)
c.1974A>C (p.Thr658=)
c.2070A>C (p.Thr690=)
n.489A>C
c.2031A>C (p.Thr677=)
c.1863A>C (p.Thr621=)
21g.25891792G>ACA127803APPn.2108C>T
n.538C>T
n.807C>T
c.2141C>T (p.Thr714Ile)
c.1916C>T (p.Thr639Ile)
c.1748C>T (p.Thr583Ile)
c.2084C>T (p.Thr695Ile)
c.2087C>T (p.Thr696Ile)
c.1811C>T (p.Thr604Ile)
c.1973C>T (p.Thr658Ile)
c.2069C>T (p.Thr690Ile)
n.488C>T
c.2030C>T (p.Thr677Ile)
c.1862C>T (p.Thr621Ile)
ClinVar dbSNP
21g.25891792G>CCA409805561APPn.2108C>G
n.538C>G
n.807C>G
c.2141C>G (p.Thr714Arg)
c.1916C>G (p.Thr639Arg)
c.1748C>G (p.Thr583Arg)
c.2084C>G (p.Thr695Arg)
c.2087C>G (p.Thr696Arg)
c.1811C>G (p.Thr604Arg)
c.1973C>G (p.Thr658Arg)
c.2069C>G (p.Thr690Arg)
n.488C>G
c.2030C>G (p.Thr677Arg)
c.1862C>G (p.Thr621Arg)
21g.25891792G=CA2383551618APPn.2108C=
n.538C=
n.807C=
c.2141C= (p.Thr714=)
c.1916C= (p.Thr639=)
c.1748C= (p.Thr583=)
c.2084C= (p.Thr695=)
c.2087C= (p.Thr696=)
c.1811C= (p.Thr604=)
c.1973C= (p.Thr658=)
c.2069C= (p.Thr690=)
n.488C=
c.2030C= (p.Thr677=)
c.1862C= (p.Thr621=)
21g.25891792G>TCA409805562APPn.2108C>A
n.538C>A
n.807C>A
c.2141C>A (p.Thr714Lys)
c.1916C>A (p.Thr639Lys)
c.1748C>A (p.Thr583Lys)
c.2084C>A (p.Thr695Lys)
c.2087C>A (p.Thr696Lys)
c.1811C>A (p.Thr604Lys)
c.1973C>A (p.Thr658Lys)
c.2069C>A (p.Thr690Lys)
n.488C>A
c.2030C>A (p.Thr677Lys)
c.1862C>A (p.Thr621Lys)
21g.25891793T>ACA409805563APPn.2107A>T
n.537A>T
n.806A>T
c.2140A>T (p.Thr714Ser)
c.1915A>T (p.Thr639Ser)
c.1747A>T (p.Thr583Ser)
c.2083A>T (p.Thr695Ser)
c.2086A>T (p.Thr696Ser)
c.1810A>T (p.Thr604Ser)
c.1972A>T (p.Thr658Ser)
c.2068A>T (p.Thr690Ser)
n.487A>T
c.2029A>T (p.Thr677Ser)
c.1861A>T (p.Thr621Ser)
21g.25891793T>CCA127814APPn.2107A>G
n.537A>G
n.806A>G
c.2140A>G (p.Thr714Ala)
c.1915A>G (p.Thr639Ala)
c.1747A>G (p.Thr583Ala)
c.2083A>G (p.Thr695Ala)
c.2086A>G (p.Thr696Ala)
c.1810A>G (p.Thr604Ala)
c.1972A>G (p.Thr658Ala)
c.2068A>G (p.Thr690Ala)
n.487A>G
c.2029A>G (p.Thr677Ala)
c.1861A>G (p.Thr621Ala)
ClinVar dbSNP COSMIC
21g.25891793T>GCA409805564APPn.2107A>C
n.537A>C
n.806A>C
c.2140A>C (p.Thr714Pro)
c.1915A>C (p.Thr639Pro)
c.1747A>C (p.Thr583Pro)
c.2083A>C (p.Thr695Pro)
c.2086A>C (p.Thr696Pro)
c.1810A>C (p.Thr604Pro)
c.1972A>C (p.Thr658Pro)
c.2068A>C (p.Thr690Pro)
n.487A>C
c.2029A>C (p.Thr677Pro)
c.1861A>C (p.Thr621Pro)
21g.25891793T=CA2383551619APPn.2107A=
n.537A=
n.806A=
c.2140A= (p.Thr714=)
c.1915A= (p.Thr639=)
c.1747A= (p.Thr583=)
c.2083A= (p.Thr695=)
c.2086A= (p.Thr696=)
c.1810A= (p.Thr604=)
c.1972A= (p.Thr658=)
c.2068A= (p.Thr690=)
n.487A=
c.2029A= (p.Thr677=)
c.1861A= (p.Thr621=)
21g.25891794C>ACA511686003APPn.2106G>T
n.536G>T
n.805G>T
c.2139G>T (p.Ala713=)
c.1914G>T (p.Ala638=)
c.1746G>T (p.Ala582=)
c.2082G>T (p.Ala694=)
c.2085G>T (p.Ala695=)
c.1809G>T (p.Ala603=)
c.1971G>T (p.Ala657=)
c.2067G>T (p.Ala689=)
n.486G>T
c.2028G>T (p.Ala676=)
c.1860G>T (p.Ala620=)
21g.25891794C=CA2383551620APPn.2106G=
n.536G=
n.805G=
c.2139G= (p.Ala713=)
c.1914G= (p.Ala638=)
c.1746G= (p.Ala582=)
c.2082G= (p.Ala694=)
c.2085G= (p.Ala695=)
c.1809G= (p.Ala603=)
c.1971G= (p.Ala657=)
c.2067G= (p.Ala689=)
n.486G=
c.2028G= (p.Ala676=)
c.1860G= (p.Ala620=)
21g.25891794C>GCA511686002APPn.2106G>C
n.536G>C
n.805G>C
c.2139G>C (p.Ala713=)
c.1914G>C (p.Ala638=)
c.1746G>C (p.Ala582=)
c.2082G>C (p.Ala694=)
c.2085G>C (p.Ala695=)
c.1809G>C (p.Ala603=)
c.1971G>C (p.Ala657=)
c.2067G>C (p.Ala689=)
n.486G>C
c.2028G>C (p.Ala676=)
c.1860G>C (p.Ala620=)
21g.25891794C>TCA9987051APPn.2106G>A
n.536G>A
n.805G>A
c.2139G>A (p.Ala713=)
c.1914G>A (p.Ala638=)
c.1746G>A (p.Ala582=)
c.2082G>A (p.Ala694=)
c.2085G>A (p.Ala695=)
c.1809G>A (p.Ala603=)
c.1971G>A (p.Ala657=)
c.2067G>A (p.Ala689=)
n.486G>A
c.2028G>A (p.Ala676=)
c.1860G>A (p.Ala620=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
21g.25891795G>ACA225505APPn.2105C>T
n.535C>T
n.804C>T
c.2138C>T (p.Ala713Val)
c.1913C>T (p.Ala638Val)
c.1745C>T (p.Ala582Val)
c.2081C>T (p.Ala694Val)
c.2084C>T (p.Ala695Val)
c.1808C>T (p.Ala603Val)
c.1970C>T (p.Ala657Val)
c.2066C>T (p.Ala689Val)
n.485C>T
c.2027C>T (p.Ala676Val)
c.1859C>T (p.Ala620Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
21g.25891795G>CCA409805565APPn.2105C>G
n.535C>G
n.804C>G
c.2138C>G (p.Ala713Gly)
c.1913C>G (p.Ala638Gly)
c.1745C>G (p.Ala582Gly)
c.2081C>G (p.Ala694Gly)
c.2084C>G (p.Ala695Gly)
c.1808C>G (p.Ala603Gly)
c.1970C>G (p.Ala657Gly)
c.2066C>G (p.Ala689Gly)
n.485C>G
c.2027C>G (p.Ala676Gly)
c.1859C>G (p.Ala620Gly)
21g.25891795G=CA2383551621APPn.2105C=
n.535C=
n.804C=
c.2138C= (p.Ala713=)
c.1913C= (p.Ala638=)
c.1745C= (p.Ala582=)
c.2081C= (p.Ala694=)
c.2084C= (p.Ala695=)
c.1808C= (p.Ala603=)
c.1970C= (p.Ala657=)
c.2066C= (p.Ala689=)
n.485C=
c.2027C= (p.Ala676=)
c.1859C= (p.Ala620=)
21g.25891795G>TCA409805566APPn.2105C>A
n.535C>A
n.804C>A
c.2138C>A (p.Ala713Glu)
c.1913C>A (p.Ala638Glu)
c.1745C>A (p.Ala582Glu)
c.2081C>A (p.Ala694Glu)
c.2084C>A (p.Ala695Glu)
c.1808C>A (p.Ala603Glu)
c.1970C>A (p.Ala657Glu)
c.2066C>A (p.Ala689Glu)
n.485C>A
c.2027C>A (p.Ala676Glu)
c.1859C>A (p.Ala620Glu)
COSMIC
21g.25891796C>ACA409805568APPn.2104G>T
n.534G>T
n.803G>T
c.2137G>T (p.Ala713Ser)
c.1912G>T (p.Ala638Ser)
c.1744G>T (p.Ala582Ser)
c.2080G>T (p.Ala694Ser)
c.2083G>T (p.Ala695Ser)
c.1807G>T (p.Ala603Ser)
c.1969G>T (p.Ala657Ser)
c.2065G>T (p.Ala689Ser)
n.484G>T
c.2026G>T (p.Ala676Ser)
c.1858G>T (p.Ala620Ser)
21g.25891796C=CA2383551622APPn.2104G=
n.534G=
n.803G=
c.2137G= (p.Ala713=)
c.1912G= (p.Ala638=)
c.1744G= (p.Ala582=)
c.2080G= (p.Ala694=)
c.2083G= (p.Ala695=)
c.1807G= (p.Ala603=)
c.1969G= (p.Ala657=)
c.2065G= (p.Ala689=)
n.484G=
c.2026G= (p.Ala676=)
c.1858G= (p.Ala620=)
21g.25891796C>GCA409805567APPn.2104G>C
n.534G>C
n.803G>C
c.2137G>C (p.Ala713Pro)
c.1912G>C (p.Ala638Pro)
c.1744G>C (p.Ala582Pro)
c.2080G>C (p.Ala694Pro)
c.2083G>C (p.Ala695Pro)
c.1807G>C (p.Ala603Pro)
c.1969G>C (p.Ala657Pro)
c.2065G>C (p.Ala689Pro)
n.484G>C
c.2026G>C (p.Ala676Pro)
c.1858G>C (p.Ala620Pro)
21g.25891796C>TCA090906APPn.2104G>A
n.534G>A
n.803G>A
c.2137G>A (p.Ala713Thr)
c.1912G>A (p.Ala638Thr)
c.1744G>A (p.Ala582Thr)
c.2080G>A (p.Ala694Thr)
c.2083G>A (p.Ala695Thr)
c.1807G>A (p.Ala603Thr)
c.1969G>A (p.Ala657Thr)
c.2065G>A (p.Ala689Thr)
n.484G>A
c.2026G>A (p.Ala676Thr)
c.1858G>A (p.Ala620Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
21g.25891797T>ACA511686004APPn.2103A>T
n.533A>T
n.802A>T
c.2136A>T (p.Ile712=)
c.1911A>T (p.Ile637=)
c.1743A>T (p.Ile581=)
c.2079A>T (p.Ile693=)
c.2082A>T (p.Ile694=)
c.1806A>T (p.Ile602=)
c.1968A>T (p.Ile656=)
c.2064A>T (p.Ile688=)
n.483A>T
c.2025A>T (p.Ile675=)
c.1857A>T (p.Ile619=)
21g.25891797T>CCA409805569APPn.2103A>G
n.533A>G
n.802A>G
c.2136A>G (p.Ile712Met)
c.1911A>G (p.Ile637Met)
c.1743A>G (p.Ile581Met)
c.2079A>G (p.Ile693Met)
c.2082A>G (p.Ile694Met)
c.1806A>G (p.Ile602Met)
c.1968A>G (p.Ile656Met)
c.2064A>G (p.Ile688Met)
n.483A>G
c.2025A>G (p.Ile675Met)
c.1857A>G (p.Ile619Met)
21g.25891797T>GCA511686005APPn.2103A>C
n.533A>C
n.802A>C
c.2136A>C (p.Ile712=)
c.1911A>C (p.Ile637=)
c.1743A>C (p.Ile581=)
c.2079A>C (p.Ile693=)
c.2082A>C (p.Ile694=)
c.1806A>C (p.Ile602=)
c.1968A>C (p.Ile656=)
c.2064A>C (p.Ile688=)
n.483A>C
c.2025A>C (p.Ile675=)
c.1857A>C (p.Ile619=)
21g.25891798A>CCA409805570APPn.2102T>G
n.532T>G
n.801T>G
c.2135T>G (p.Ile712Arg)
c.1910T>G (p.Ile637Arg)
c.1742T>G (p.Ile581Arg)
c.2078T>G (p.Ile693Arg)
c.2081T>G (p.Ile694Arg)
c.1805T>G (p.Ile602Arg)
c.1967T>G (p.Ile656Arg)
c.2063T>G (p.Ile688Arg)
n.482T>G
c.2024T>G (p.Ile675Arg)
c.1856T>G (p.Ile619Arg)
21g.25891798A>GCA409805571APPn.2102T>C
n.532T>C
n.801T>C
c.2135T>C (p.Ile712Thr)
c.1910T>C (p.Ile637Thr)
c.1742T>C (p.Ile581Thr)
c.2078T>C (p.Ile693Thr)
c.2081T>C (p.Ile694Thr)
c.1805T>C (p.Ile602Thr)
c.1967T>C (p.Ile656Thr)
c.2063T>C (p.Ile688Thr)
n.482T>C
c.2024T>C (p.Ile675Thr)
c.1856T>C (p.Ile619Thr)
21g.25891798A>TCA409805572APPn.2102T>A
n.532T>A
n.801T>A
c.2135T>A (p.Ile712Lys)
c.1910T>A (p.Ile637Lys)
c.1742T>A (p.Ile581Lys)
c.2078T>A (p.Ile693Lys)
c.2081T>A (p.Ile694Lys)
c.1805T>A (p.Ile602Lys)
c.1967T>A (p.Ile656Lys)
c.2063T>A (p.Ile688Lys)
n.482T>A
c.2024T>A (p.Ile675Lys)
c.1856T>A (p.Ile619Lys)

Number of alleles fetched