Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.22272831G>ACA379923702ANO5n.94G>A
c.1627G>A (p.Ala543Thr)
c.2035G>A (p.Ala679Thr)
n.3071G>A
c.2032G>A (p.Ala678Thr)
c.2077G>A (p.Ala693Thr)
n.2412G>A
c.2074G>A (p.Ala692Thr)
c.1999G>A (p.Ala667Thr)
c.1996G>A (p.Ala666Thr)
c.1984G>A (p.Ala662Thr)
11g.22272831G>CCA379923706ANO5n.94G>C
c.1627G>C (p.Ala543Pro)
c.2035G>C (p.Ala679Pro)
n.3071G>C
c.2032G>C (p.Ala678Pro)
c.2077G>C (p.Ala693Pro)
n.2412G>C
c.2074G>C (p.Ala692Pro)
c.1999G>C (p.Ala667Pro)
c.1996G>C (p.Ala666Pro)
c.1984G>C (p.Ala662Pro)
dbSNP gnomAD v2
11g.22272831G=CA1957402780ANO5n.94G=
c.1627G= (p.Ala543=)
c.2035G= (p.Ala679=)
n.3071G=
c.2032G= (p.Ala678=)
c.2077G= (p.Ala693=)
n.2412G=
c.2074G= (p.Ala692=)
c.1999G= (p.Ala667=)
c.1996G= (p.Ala666=)
c.1984G= (p.Ala662=)
11g.22272831G>TCA379923704ANO5n.94G>T
c.1627G>T (p.Ala543Ser)
c.2035G>T (p.Ala679Ser)
n.3071G>T
c.2032G>T (p.Ala678Ser)
c.2077G>T (p.Ala693Ser)
n.2412G>T
c.2074G>T (p.Ala692Ser)
c.1999G>T (p.Ala667Ser)
c.1996G>T (p.Ala666Ser)
c.1984G>T (p.Ala662Ser)
11g.22272832C>ACA379923707ANO5n.95C>A
c.1628C>A (p.Ala543Asp)
c.2036C>A (p.Ala679Asp)
n.3072C>A
c.2033C>A (p.Ala678Asp)
c.2078C>A (p.Ala693Asp)
n.2413C>A
c.2075C>A (p.Ala692Asp)
c.2000C>A (p.Ala667Asp)
c.1997C>A (p.Ala666Asp)
c.1985C>A (p.Ala662Asp)
11g.22272832C>GCA379923711ANO5n.95C>G
c.1628C>G (p.Ala543Gly)
c.2036C>G (p.Ala679Gly)
n.3072C>G
c.2033C>G (p.Ala678Gly)
c.2078C>G (p.Ala693Gly)
n.2413C>G
c.2075C>G (p.Ala692Gly)
c.2000C>G (p.Ala667Gly)
c.1997C>G (p.Ala666Gly)
c.1985C>G (p.Ala662Gly)
11g.22272832C>TCA379923709ANO5n.95C>T
c.1628C>T (p.Ala543Val)
c.2036C>T (p.Ala679Val)
n.3072C>T
c.2033C>T (p.Ala678Val)
c.2078C>T (p.Ala693Val)
n.2413C>T
c.2075C>T (p.Ala692Val)
c.2000C>T (p.Ala667Val)
c.1997C>T (p.Ala666Val)
c.1985C>T (p.Ala662Val)
11g.22272833T>ACA473407500ANO5n.96T>A
c.1629T>A (p.Ala543=)
c.2037T>A (p.Ala679=)
n.3073T>A
c.2034T>A (p.Ala678=)
c.2079T>A (p.Ala693=)
n.2414T>A
c.2076T>A (p.Ala692=)
c.2001T>A (p.Ala667=)
c.1998T>A (p.Ala666=)
c.1986T>A (p.Ala662=)
11g.22272833T>CCA473407501ANO5n.96T>C
c.1629T>C (p.Ala543=)
c.2037T>C (p.Ala679=)
n.3073T>C
c.2034T>C (p.Ala678=)
c.2079T>C (p.Ala693=)
n.2414T>C
c.2076T>C (p.Ala692=)
c.2001T>C (p.Ala667=)
c.1998T>C (p.Ala666=)
c.1986T>C (p.Ala662=)
gnomAD v4
11g.22272833T>GCA473407502ANO5n.96T>G
c.1629T>G (p.Ala543=)
c.2037T>G (p.Ala679=)
n.3073T>G
c.2034T>G (p.Ala678=)
c.2079T>G (p.Ala693=)
n.2414T>G
c.2076T>G (p.Ala692=)
c.2001T>G (p.Ala667=)
c.1998T>G (p.Ala666=)
c.1986T>G (p.Ala662=)
11g.22272834C>ACA379923713ANO5n.97C>A
c.1630C>A (p.Pro544Thr)
c.2038C>A (p.Pro680Thr)
n.3074C>A
c.2035C>A (p.Pro679Thr)
c.2080C>A (p.Pro694Thr)
n.2415C>A
c.2077C>A (p.Pro693Thr)
c.2002C>A (p.Pro668Thr)
c.1999C>A (p.Pro667Thr)
c.1987C>A (p.Pro663Thr)
COSMIC
11g.22272834C=CA1957402791ANO5n.97C=
c.1630C= (p.Pro544=)
c.2038C= (p.Pro680=)
n.3074C=
c.2035C= (p.Pro679=)
c.2080C= (p.Pro694=)
n.2415C=
c.2077C= (p.Pro693=)
c.2002C= (p.Pro668=)
c.1999C= (p.Pro667=)
c.1987C= (p.Pro663=)
11g.22272834C>GCA379923714ANO5n.97C>G
c.1630C>G (p.Pro544Ala)
c.2038C>G (p.Pro680Ala)
n.3074C>G
c.2035C>G (p.Pro679Ala)
c.2080C>G (p.Pro694Ala)
n.2415C>G
c.2077C>G (p.Pro693Ala)
c.2002C>G (p.Pro668Ala)
c.1999C>G (p.Pro667Ala)
c.1987C>G (p.Pro663Ala)
11g.22272834C>TCA10604433ANO5n.97C>T
c.1630C>T (p.Pro544Ser)
c.2038C>T (p.Pro680Ser)
n.3074C>T
c.2035C>T (p.Pro679Ser)
c.2080C>T (p.Pro694Ser)
n.2415C>T
c.2077C>T (p.Pro693Ser)
c.2002C>T (p.Pro668Ser)
c.1999C>T (p.Pro667Ser)
c.1987C>T (p.Pro663Ser)
ClinVar dbSNP
11g.22272835C>ACA379923716ANO5n.98C>A
c.1631C>A (p.Pro544His)
c.2039C>A (p.Pro680His)
n.3075C>A
c.2036C>A (p.Pro679His)
c.2081C>A (p.Pro694His)
n.2416C>A
c.2078C>A (p.Pro693His)
c.2003C>A (p.Pro668His)
c.2000C>A (p.Pro667His)
c.1988C>A (p.Pro663His)
11g.22272835C>GCA379923718ANO5n.98C>G
c.1631C>G (p.Pro544Arg)
c.2039C>G (p.Pro680Arg)
n.3075C>G
c.2036C>G (p.Pro679Arg)
c.2081C>G (p.Pro694Arg)
n.2416C>G
c.2078C>G (p.Pro693Arg)
c.2003C>G (p.Pro668Arg)
c.2000C>G (p.Pro667Arg)
c.1988C>G (p.Pro663Arg)
11g.22272835C>TCA379923720ANO5n.98C>T
c.1631C>T (p.Pro544Leu)
c.2039C>T (p.Pro680Leu)
n.3075C>T
c.2036C>T (p.Pro679Leu)
c.2081C>T (p.Pro694Leu)
n.2416C>T
c.2078C>T (p.Pro693Leu)
c.2003C>T (p.Pro668Leu)
c.2000C>T (p.Pro667Leu)
c.1988C>T (p.Pro663Leu)
11g.22272836T>ACA473407503ANO5n.99T>A
c.1632T>A (p.Pro544=)
c.2040T>A (p.Pro680=)
n.3076T>A
c.2037T>A (p.Pro679=)
c.2082T>A (p.Pro694=)
n.2417T>A
c.2079T>A (p.Pro693=)
c.2004T>A (p.Pro668=)
c.2001T>A (p.Pro667=)
c.1989T>A (p.Pro663=)
11g.22272836T>CCA473407504ANO5n.99T>C
c.1632T>C (p.Pro544=)
c.2040T>C (p.Pro680=)
n.3076T>C
c.2037T>C (p.Pro679=)
c.2082T>C (p.Pro694=)
n.2417T>C
c.2079T>C (p.Pro693=)
c.2004T>C (p.Pro668=)
c.2001T>C (p.Pro667=)
c.1989T>C (p.Pro663=)
11g.22272836T>GCA473407505ANO5n.99T>G
c.1632T>G (p.Pro544=)
c.2040T>G (p.Pro680=)
n.3076T>G
c.2037T>G (p.Pro679=)
c.2082T>G (p.Pro694=)
n.2417T>G
c.2079T>G (p.Pro693=)
c.2004T>G (p.Pro668=)
c.2001T>G (p.Pro667=)
c.1989T>G (p.Pro663=)
dbSNP gnomAD v4
11g.22272836T=CA1957402801ANO5n.99T=
c.1632T= (p.Pro544=)
c.2040T= (p.Pro680=)
n.3076T=
c.2037T= (p.Pro679=)
c.2082T= (p.Pro694=)
n.2417T=
c.2079T= (p.Pro693=)
c.2004T= (p.Pro668=)
c.2001T= (p.Pro667=)
c.1989T= (p.Pro663=)
11g.22272837C>ACA379923721ANO5n.100C>A
c.1633C>A (p.Leu545Ile)
c.2041C>A (p.Leu681Ile)
n.3077C>A
c.2038C>A (p.Leu680Ile)
c.2083C>A (p.Leu695Ile)
n.2418C>A
c.2080C>A (p.Leu694Ile)
c.2005C>A (p.Leu669Ile)
c.2002C>A (p.Leu668Ile)
c.1990C>A (p.Leu664Ile)
11g.22272837C>GCA379923723ANO5n.100C>G
c.1633C>G (p.Leu545Val)
c.2041C>G (p.Leu681Val)
n.3077C>G
c.2038C>G (p.Leu680Val)
c.2083C>G (p.Leu695Val)
n.2418C>G
c.2080C>G (p.Leu694Val)
c.2005C>G (p.Leu669Val)
c.2002C>G (p.Leu668Val)
c.1990C>G (p.Leu664Val)
11g.22272837C>TCA379923724ANO5n.100C>T
c.1633C>T (p.Leu545Phe)
c.2041C>T (p.Leu681Phe)
n.3077C>T
c.2038C>T (p.Leu680Phe)
c.2083C>T (p.Leu695Phe)
n.2418C>T
c.2080C>T (p.Leu694Phe)
c.2005C>T (p.Leu669Phe)
c.2002C>T (p.Leu668Phe)
c.1990C>T (p.Leu664Phe)
gnomAD v4
11g.22272838T>ACA379923726ANO5n.101T>A
c.1634T>A (p.Leu545His)
c.2042T>A (p.Leu681His)
n.3078T>A
c.2039T>A (p.Leu680His)
c.2084T>A (p.Leu695His)
n.2419T>A
c.2081T>A (p.Leu694His)
c.2006T>A (p.Leu669His)
c.2003T>A (p.Leu668His)
c.1991T>A (p.Leu664His)
11g.22272838T>CCA379923728ANO5n.101T>C
c.1634T>C (p.Leu545Pro)
c.2042T>C (p.Leu681Pro)
n.3078T>C
c.2039T>C (p.Leu680Pro)
c.2084T>C (p.Leu695Pro)
n.2419T>C
c.2081T>C (p.Leu694Pro)
c.2006T>C (p.Leu669Pro)
c.2003T>C (p.Leu668Pro)
c.1991T>C (p.Leu664Pro)
11g.22272838T>GCA379923729ANO5n.101T>G
c.1634T>G (p.Leu545Arg)
c.2042T>G (p.Leu681Arg)
n.3078T>G
c.2039T>G (p.Leu680Arg)
c.2084T>G (p.Leu695Arg)
n.2419T>G
c.2081T>G (p.Leu694Arg)
c.2006T>G (p.Leu669Arg)
c.2003T>G (p.Leu668Arg)
c.1991T>G (p.Leu664Arg)
11g.22272839T>ACA473407506ANO5n.102T>A
c.1635T>A (p.Leu545=)
c.2043T>A (p.Leu681=)
n.3079T>A
c.2040T>A (p.Leu680=)
c.2085T>A (p.Leu695=)
n.2420T>A
c.2082T>A (p.Leu694=)
c.2007T>A (p.Leu669=)
c.2004T>A (p.Leu668=)
c.1992T>A (p.Leu664=)
COSMIC
11g.22272839T>CCA473407507ANO5n.102T>C
c.1635T>C (p.Leu545=)
c.2043T>C (p.Leu681=)
n.3079T>C
c.2040T>C (p.Leu680=)
c.2085T>C (p.Leu695=)
n.2420T>C
c.2082T>C (p.Leu694=)
c.2007T>C (p.Leu669=)
c.2004T>C (p.Leu668=)
c.1992T>C (p.Leu664=)
dbSNP gnomAD v4
11g.22272839T>GCA473407508ANO5n.102T>G
c.1635T>G (p.Leu545=)
c.2043T>G (p.Leu681=)
n.3079T>G
c.2040T>G (p.Leu680=)
c.2085T>G (p.Leu695=)
n.2420T>G
c.2082T>G (p.Leu694=)
c.2007T>G (p.Leu669=)
c.2004T>G (p.Leu668=)
c.1992T>G (p.Leu664=)
11g.22272839T=CA1957402803ANO5n.102T=
c.1635T= (p.Leu545=)
c.2043T= (p.Leu681=)
n.3079T=
c.2040T= (p.Leu680=)
c.2085T= (p.Leu695=)
n.2420T=
c.2082T= (p.Leu694=)
c.2007T= (p.Leu669=)
c.2004T= (p.Leu668=)
c.1992T= (p.Leu664=)
11g.22272840C>ACA379923730ANO5n.103C>A
c.1636C>A (p.Leu546Ile)
c.2044C>A (p.Leu682Ile)
n.3080C>A
c.2041C>A (p.Leu681Ile)
c.2086C>A (p.Leu696Ile)
n.2421C>A
c.2083C>A (p.Leu695Ile)
c.2008C>A (p.Leu670Ile)
c.2005C>A (p.Leu669Ile)
c.1993C>A (p.Leu665Ile)
11g.22272840C>GCA379923733ANO5n.103C>G
c.1636C>G (p.Leu546Val)
c.2044C>G (p.Leu682Val)
n.3080C>G
c.2041C>G (p.Leu681Val)
c.2086C>G (p.Leu696Val)
n.2421C>G
c.2083C>G (p.Leu695Val)
c.2008C>G (p.Leu670Val)
c.2005C>G (p.Leu669Val)
c.1993C>G (p.Leu665Val)
gnomAD v4
11g.22272840C>TCA379923732ANO5n.103C>T
c.1636C>T (p.Leu546Phe)
c.2044C>T (p.Leu682Phe)
n.3080C>T
c.2041C>T (p.Leu681Phe)
c.2086C>T (p.Leu696Phe)
n.2421C>T
c.2083C>T (p.Leu695Phe)
c.2008C>T (p.Leu670Phe)
c.2005C>T (p.Leu669Phe)
c.1993C>T (p.Leu665Phe)
COSMIC
11g.22272841T>ACA379923734ANO5n.104T>A
c.1637T>A (p.Leu546His)
c.2045T>A (p.Leu682His)
n.3081T>A
c.2042T>A (p.Leu681His)
c.2087T>A (p.Leu696His)
n.2422T>A
c.2084T>A (p.Leu695His)
c.2009T>A (p.Leu670His)
c.2006T>A (p.Leu669His)
c.1994T>A (p.Leu665His)
gnomAD v4
11g.22272841T>CCA218775800ANO5n.104T>C
c.1637T>C (p.Leu546Pro)
c.2045T>C (p.Leu682Pro)
n.3081T>C
c.2042T>C (p.Leu681Pro)
c.2087T>C (p.Leu696Pro)
n.2422T>C
c.2084T>C (p.Leu695Pro)
c.2009T>C (p.Leu670Pro)
c.2006T>C (p.Leu669Pro)
c.1994T>C (p.Leu665Pro)
dbSNP
11g.22272841T>GCA379923736ANO5n.104T>G
c.1637T>G (p.Leu546Arg)
c.2045T>G (p.Leu682Arg)
n.3081T>G
c.2042T>G (p.Leu681Arg)
c.2087T>G (p.Leu696Arg)
n.2422T>G
c.2084T>G (p.Leu695Arg)
c.2009T>G (p.Leu670Arg)
c.2006T>G (p.Leu669Arg)
c.1994T>G (p.Leu665Arg)
11g.22272841T=CA1957402810ANO5n.104T=
c.1637T= (p.Leu546=)
c.2045T= (p.Leu682=)
n.3081T=
c.2042T= (p.Leu681=)
c.2087T= (p.Leu696=)
n.2422T=
c.2084T= (p.Leu695=)
c.2009T= (p.Leu670=)
c.2006T= (p.Leu669=)
c.1994T= (p.Leu665=)
11g.22272842T>ACA473407509ANO5n.105T>A
c.1638T>A (p.Leu546=)
c.2046T>A (p.Leu682=)
n.3082T>A
c.2043T>A (p.Leu681=)
c.2088T>A (p.Leu696=)
n.2423T>A
c.2085T>A (p.Leu695=)
c.2010T>A (p.Leu670=)
c.2007T>A (p.Leu669=)
c.1995T>A (p.Leu665=)
11g.22272842T>CCA5923454ANO5n.105T>C
c.1638T>C (p.Leu546=)
c.2046T>C (p.Leu682=)
n.3082T>C
c.2043T>C (p.Leu681=)
c.2088T>C (p.Leu696=)
n.2423T>C
c.2085T>C (p.Leu695=)
c.2010T>C (p.Leu670=)
c.2007T>C (p.Leu669=)
c.1995T>C (p.Leu665=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.22272842T>GCA473407510ANO5n.105T>G
c.1638T>G (p.Leu546=)
c.2046T>G (p.Leu682=)
n.3082T>G
c.2043T>G (p.Leu681=)
c.2088T>G (p.Leu696=)
n.2423T>G
c.2085T>G (p.Leu695=)
c.2010T>G (p.Leu670=)
c.2007T>G (p.Leu669=)
c.1995T>G (p.Leu665=)
11g.22272842T=CA1957402818ANO5n.105T=
c.1638T= (p.Leu546=)
c.2046T= (p.Leu682=)
n.3082T=
c.2043T= (p.Leu681=)
c.2088T= (p.Leu696=)
n.2423T=
c.2085T= (p.Leu695=)
c.2010T= (p.Leu670=)
c.2007T= (p.Leu669=)
c.1995T= (p.Leu665=)
11g.22272843G>ACA379923739ANO5n.106G>A
c.1639G>A (p.Ala547Thr)
c.2047G>A (p.Ala683Thr)
n.3083G>A
c.2044G>A (p.Ala682Thr)
c.2089G>A (p.Ala697Thr)
n.2424G>A
c.2086G>A (p.Ala696Thr)
c.2011G>A (p.Ala671Thr)
c.2008G>A (p.Ala670Thr)
c.1996G>A (p.Ala666Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.22272843G>CCA379923740ANO5n.106G>C
c.1639G>C (p.Ala547Pro)
c.2047G>C (p.Ala683Pro)
n.3083G>C
c.2044G>C (p.Ala682Pro)
c.2089G>C (p.Ala697Pro)
n.2424G>C
c.2086G>C (p.Ala696Pro)
c.2011G>C (p.Ala671Pro)
c.2008G>C (p.Ala670Pro)
c.1996G>C (p.Ala666Pro)
11g.22272843G=CA1957402852ANO5n.106G=
c.1639G= (p.Ala547=)
c.2047G= (p.Ala683=)
n.3083G=
c.2044G= (p.Ala682=)
c.2089G= (p.Ala697=)
n.2424G=
c.2086G= (p.Ala696=)
c.2011G= (p.Ala671=)
c.2008G= (p.Ala670=)
c.1996G= (p.Ala666=)
11g.22272843G>TCA379923741ANO5n.106G>T
c.1639G>T (p.Ala547Ser)
c.2047G>T (p.Ala683Ser)
n.3083G>T
c.2044G>T (p.Ala682Ser)
c.2089G>T (p.Ala697Ser)
n.2424G>T
c.2086G>T (p.Ala696Ser)
c.2011G>T (p.Ala671Ser)
c.2008G>T (p.Ala670Ser)
c.1996G>T (p.Ala666Ser)
11g.22272844C>ACA379923743ANO5n.107C>A
c.1640C>A (p.Ala547Asp)
c.2048C>A (p.Ala683Asp)
n.3084C>A
c.2045C>A (p.Ala682Asp)
c.2090C>A (p.Ala697Asp)
n.2425C>A
c.2087C>A (p.Ala696Asp)
c.2012C>A (p.Ala671Asp)
c.2009C>A (p.Ala670Asp)
c.1997C>A (p.Ala666Asp)
11g.22272844C>GCA379923745ANO5n.107C>G
c.1640C>G (p.Ala547Gly)
c.2048C>G (p.Ala683Gly)
n.3084C>G
c.2045C>G (p.Ala682Gly)
c.2090C>G (p.Ala697Gly)
n.2425C>G
c.2087C>G (p.Ala696Gly)
c.2012C>G (p.Ala671Gly)
c.2009C>G (p.Ala670Gly)
c.1997C>G (p.Ala666Gly)
11g.22272844C>TCA379923746ANO5n.107C>T
c.1640C>T (p.Ala547Val)
c.2048C>T (p.Ala683Val)
n.3084C>T
c.2045C>T (p.Ala682Val)
c.2090C>T (p.Ala697Val)
n.2425C>T
c.2087C>T (p.Ala696Val)
c.2012C>T (p.Ala671Val)
c.2009C>T (p.Ala670Val)
c.1997C>T (p.Ala666Val)
11g.22272845T>ACA473407511ANO5n.108T>A
c.1641T>A (p.Ala547=)
c.2049T>A (p.Ala683=)
n.3085T>A
c.2046T>A (p.Ala682=)
c.2091T>A (p.Ala697=)
n.2426T>A
c.2088T>A (p.Ala696=)
c.2013T>A (p.Ala671=)
c.2010T>A (p.Ala670=)
c.1998T>A (p.Ala666=)

Number of alleles fetched