Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.27926139A>CCA391360898OCA2c.2067T>G (p.Phe689Leu)
c.1995T>G (p.Phe665Leu)
c.2091T>G (p.Phe697Leu)
c.2019T>G (p.Phe673Leu)
c.1953T>G (p.Phe651Leu)
c.1896T>G (p.Phe632Leu)
15g.27926139A>GCA488959254OCA2c.2067T>C (p.Phe689=)
c.1995T>C (p.Phe665=)
c.2091T>C (p.Phe697=)
c.2019T>C (p.Phe673=)
c.1953T>C (p.Phe651=)
c.1896T>C (p.Phe632=)
gnomAD v4
15g.27926139A>TCA391360901OCA2c.2067T>A (p.Phe689Leu)
c.1995T>A (p.Phe665Leu)
c.2091T>A (p.Phe697Leu)
c.2019T>A (p.Phe673Leu)
c.1953T>A (p.Phe651Leu)
c.1896T>A (p.Phe632Leu)
15g.27926140A>CCA391360904OCA2c.2066T>G (p.Phe689Cys)
c.1994T>G (p.Phe665Cys)
c.2090T>G (p.Phe697Cys)
c.2018T>G (p.Phe673Cys)
c.1952T>G (p.Phe651Cys)
c.1895T>G (p.Phe632Cys)
15g.27926140A>GCA391360907OCA2c.2066T>C (p.Phe689Ser)
c.1994T>C (p.Phe665Ser)
c.2090T>C (p.Phe697Ser)
c.2018T>C (p.Phe673Ser)
c.1952T>C (p.Phe651Ser)
c.1895T>C (p.Phe632Ser)
15g.27926140A>TCA391360909OCA2c.2066T>A (p.Phe689Tyr)
c.1994T>A (p.Phe665Tyr)
c.2090T>A (p.Phe697Tyr)
c.2018T>A (p.Phe673Tyr)
c.1952T>A (p.Phe651Tyr)
c.1895T>A (p.Phe632Tyr)
15g.27926141A>CCA391360912OCA2c.2065T>G (p.Phe689Val)
c.1993T>G (p.Phe665Val)
c.2089T>G (p.Phe697Val)
c.2017T>G (p.Phe673Val)
c.1951T>G (p.Phe651Val)
c.1894T>G (p.Phe632Val)
15g.27926141A>GCA391360915OCA2c.2065T>C (p.Phe689Leu)
c.1993T>C (p.Phe665Leu)
c.2089T>C (p.Phe697Leu)
c.2017T>C (p.Phe673Leu)
c.1951T>C (p.Phe651Leu)
c.1894T>C (p.Phe632Leu)
15g.27926141A>TCA391360917OCA2c.2065T>A (p.Phe689Ile)
c.1993T>A (p.Phe665Ile)
c.2089T>A (p.Phe697Ile)
c.2017T>A (p.Phe673Ile)
c.1951T>A (p.Phe651Ile)
c.1894T>A (p.Phe632Ile)
15g.27926142G>ACA488959255OCA2c.2064C>T (p.Leu688=)
c.1992C>T (p.Leu664=)
c.2088C>T (p.Leu696=)
c.2016C>T (p.Leu672=)
c.1950C>T (p.Leu650=)
c.1893C>T (p.Leu631=)
15g.27926142G>CCA488959256OCA2c.2064C>G (p.Leu688=)
c.1992C>G (p.Leu664=)
c.2088C>G (p.Leu696=)
c.2016C>G (p.Leu672=)
c.1950C>G (p.Leu650=)
c.1893C>G (p.Leu631=)
gnomAD v4
15g.27926142G>TCA488959257OCA2c.2064C>A (p.Leu688=)
c.1992C>A (p.Leu664=)
c.2088C>A (p.Leu696=)
c.2016C>A (p.Leu672=)
c.1950C>A (p.Leu650=)
c.1893C>A (p.Leu631=)
15g.27926143A=CA2166365054OCA2c.2063T= (p.Leu688=)
c.1991T= (p.Leu664=)
c.2087T= (p.Leu696=)
c.2015T= (p.Leu672=)
c.1949T= (p.Leu650=)
c.1892T= (p.Leu631=)
15g.27926143A>CCA391360919OCA2c.2063T>G (p.Leu688Arg)
c.1991T>G (p.Leu664Arg)
c.2087T>G (p.Leu696Arg)
c.2015T>G (p.Leu672Arg)
c.1949T>G (p.Leu650Arg)
c.1892T>G (p.Leu631Arg)
15g.27926143A>GCA7438778OCA2c.2063T>C (p.Leu688Pro)
c.1991T>C (p.Leu664Pro)
c.2087T>C (p.Leu696Pro)
c.2015T>C (p.Leu672Pro)
c.1949T>C (p.Leu650Pro)
c.1892T>C (p.Leu631Pro)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.27926143A>TCA391360926OCA2c.2063T>A (p.Leu688His)
c.1991T>A (p.Leu664His)
c.2087T>A (p.Leu696His)
c.2015T>A (p.Leu672His)
c.1949T>A (p.Leu650His)
c.1892T>A (p.Leu631His)
15g.27926144G>ACA391360936OCA2c.2062C>T (p.Leu688Phe)
c.1990C>T (p.Leu664Phe)
c.2086C>T (p.Leu696Phe)
c.2014C>T (p.Leu672Phe)
c.1948C>T (p.Leu650Phe)
c.1891C>T (p.Leu631Phe)
ClinVar
15g.27926144G>CCA391360933OCA2c.2062C>G (p.Leu688Val)
c.1990C>G (p.Leu664Val)
c.2086C>G (p.Leu696Val)
c.2014C>G (p.Leu672Val)
c.1948C>G (p.Leu650Val)
c.1891C>G (p.Leu631Val)
15g.27926144G>TCA391360929OCA2c.2062C>A (p.Leu688Ile)
c.1990C>A (p.Leu664Ile)
c.2086C>A (p.Leu696Ile)
c.2014C>A (p.Leu672Ile)
c.1948C>A (p.Leu650Ile)
c.1891C>A (p.Leu631Ile)
15g.27926145C>ACA488959258OCA2c.2061G>T (p.Ala687=)
c.1989G>T (p.Ala663=)
c.2085G>T (p.Ala695=)
c.2013G>T (p.Ala671=)
c.1947G>T (p.Ala649=)
c.1890G>T (p.Ala630=)
COSMIC
15g.27926145C=CA2166365055OCA2c.2061G= (p.Ala687=)
c.1989G= (p.Ala663=)
c.2085G= (p.Ala695=)
c.2013G= (p.Ala671=)
c.1947G= (p.Ala649=)
c.1890G= (p.Ala630=)
15g.27926145C>GCA488959259OCA2c.2061G>C (p.Ala687=)
c.1989G>C (p.Ala663=)
c.2085G>C (p.Ala695=)
c.2013G>C (p.Ala671=)
c.1947G>C (p.Ala649=)
c.1890G>C (p.Ala630=)
15g.27926145C>TCA7438779OCA2c.2061G>A (p.Ala687=)
c.1989G>A (p.Ala663=)
c.2085G>A (p.Ala695=)
c.2013G>A (p.Ala671=)
c.1947G>A (p.Ala649=)
c.1890G>A (p.Ala630=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.27926145_27926148dupCA2627379624OCA2c.2058_2061dup (p.Leu688SerfsTer?)
c.1986_1989dup (p.Leu664SerfsTer?)
c.2082_2085dup (p.Leu696SerfsTer?)
c.2010_2013dup (p.Leu672SerfsTer?)
c.1944_1947dup (p.Leu650SerfsTer?)
c.2082_2085dup (p.Leu696SerfsTer19)
c.1887_1890dup (p.Leu631SerfsTer?)
gnomAD v4
15g.27926146G>ACA7438780OCA2c.2060C>T (p.Ala687Val)
c.1988C>T (p.Ala663Val)
c.2084C>T (p.Ala695Val)
c.2012C>T (p.Ala671Val)
c.1946C>T (p.Ala649Val)
c.1889C>T (p.Ala630Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.27926146G>CCA391360943OCA2c.2060C>G (p.Ala687Gly)
c.1988C>G (p.Ala663Gly)
c.2084C>G (p.Ala695Gly)
c.2012C>G (p.Ala671Gly)
c.1946C>G (p.Ala649Gly)
c.1889C>G (p.Ala630Gly)
15g.27926146G=CA2166365056OCA2c.2060C= (p.Ala687=)
c.1988C= (p.Ala663=)
c.2084C= (p.Ala695=)
c.2012C= (p.Ala671=)
c.1946C= (p.Ala649=)
c.1889C= (p.Ala630=)
15g.27926146G>TCA391360946OCA2c.2060C>A (p.Ala687Glu)
c.1988C>A (p.Ala663Glu)
c.2084C>A (p.Ala695Glu)
c.2012C>A (p.Ala671Glu)
c.1946C>A (p.Ala649Glu)
c.1889C>A (p.Ala630Glu)
dbSNP gnomAD v4
15g.27926147C>ACA391360948OCA2c.2059G>T (p.Ala687Ser)
c.1987G>T (p.Ala663Ser)
c.2083G>T (p.Ala695Ser)
c.2011G>T (p.Ala671Ser)
c.1945G>T (p.Ala649Ser)
c.1888G>T (p.Ala630Ser)
15g.27926147C=CA2166365057OCA2c.2059G= (p.Ala687=)
c.1987G= (p.Ala663=)
c.2083G= (p.Ala695=)
c.2011G= (p.Ala671=)
c.1945G= (p.Ala649=)
c.1888G= (p.Ala630=)
15g.27926147C>GCA391360951OCA2c.2059G>C (p.Ala687Pro)
c.1987G>C (p.Ala663Pro)
c.2083G>C (p.Ala695Pro)
c.2011G>C (p.Ala671Pro)
c.1945G>C (p.Ala649Pro)
c.1888G>C (p.Ala630Pro)
15g.27926147C>TCA391360952OCA2c.2059G>A (p.Ala687Thr)
c.1987G>A (p.Ala663Thr)
c.2083G>A (p.Ala695Thr)
c.2011G>A (p.Ala671Thr)
c.1945G>A (p.Ala649Thr)
c.1888G>A (p.Ala630Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.27926148T>ACA7438782OCA2c.2058A>T (p.Ala686=)
c.1986A>T (p.Ala662=)
c.2082A>T (p.Ala694=)
c.2010A>T (p.Ala670=)
c.1944A>T (p.Ala648=)
c.1887A>T (p.Ala629=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.27926148T>CCA488959260OCA2c.2058A>G (p.Ala686=)
c.1986A>G (p.Ala662=)
c.2082A>G (p.Ala694=)
c.2010A>G (p.Ala670=)
c.1944A>G (p.Ala648=)
c.1887A>G (p.Ala629=)
15g.27926148T>GCA7438781OCA2c.2058A>C (p.Ala686=)
c.1986A>C (p.Ala662=)
c.2082A>C (p.Ala694=)
c.2010A>C (p.Ala670=)
c.1944A>C (p.Ala648=)
c.1887A>C (p.Ala629=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.27926148T=CA2166365058OCA2c.2058A= (p.Ala686=)
c.1986A= (p.Ala662=)
c.2082A= (p.Ala694=)
c.2010A= (p.Ala670=)
c.1944A= (p.Ala648=)
c.1887A= (p.Ala629=)
15g.27926149G>ACA267867140OCA2c.2057C>T (p.Ala686Val)
c.1985C>T (p.Ala662Val)
c.2081C>T (p.Ala694Val)
c.2009C>T (p.Ala670Val)
c.1943C>T (p.Ala648Val)
c.1886C>T (p.Ala629Val)
dbSNP gnomAD v3 gnomAD v4
15g.27926149G>CCA391360963OCA2c.2057C>G (p.Ala686Gly)
c.1985C>G (p.Ala662Gly)
c.2081C>G (p.Ala694Gly)
c.2009C>G (p.Ala670Gly)
c.1943C>G (p.Ala648Gly)
c.1886C>G (p.Ala629Gly)
15g.27926149G=CA2166365059OCA2c.2057C= (p.Ala686=)
c.1985C= (p.Ala662=)
c.2081C= (p.Ala694=)
c.2009C= (p.Ala670=)
c.1943C= (p.Ala648=)
c.1886C= (p.Ala629=)
15g.27926149G>TCA391360968OCA2c.2057C>A (p.Ala686Glu)
c.1985C>A (p.Ala662Glu)
c.2081C>A (p.Ala694Glu)
c.2009C>A (p.Ala670Glu)
c.1943C>A (p.Ala648Glu)
c.1886C>A (p.Ala629Glu)
dbSNP gnomAD v2 gnomAD v4
15g.27926150C>ACA391360973OCA2c.2056G>T (p.Ala686Ser)
c.1984G>T (p.Ala662Ser)
c.2080G>T (p.Ala694Ser)
c.2008G>T (p.Ala670Ser)
c.1942G>T (p.Ala648Ser)
c.1885G>T (p.Ala629Ser)
15g.27926150C>GCA391360971OCA2c.2056G>C (p.Ala686Pro)
c.1984G>C (p.Ala662Pro)
c.2080G>C (p.Ala694Pro)
c.2008G>C (p.Ala670Pro)
c.1942G>C (p.Ala648Pro)
c.1885G>C (p.Ala629Pro)
15g.27926150C>TCA391360970OCA2c.2056G>A (p.Ala686Thr)
c.1984G>A (p.Ala662Thr)
c.2080G>A (p.Ala694Thr)
c.2008G>A (p.Ala670Thr)
c.1942G>A (p.Ala648Thr)
c.1885G>A (p.Ala629Thr)
15g.27926150_27926151delinsCACA2166365060OCA2c.2055_2056delinsTG (p.Phe685=)
c.1983_1984delinsTG (p.Phe661=)
c.2079_2080delinsTG (p.Phe693=)
c.2007_2008delinsTG (p.Phe669=)
c.1941_1942delinsTG (p.Phe647=)
c.1884_1885delinsTG (p.Phe628=)
15g.27926151A>CCA391360983OCA2c.2055T>G (p.Phe685Leu)
c.1983T>G (p.Phe661Leu)
c.2079T>G (p.Phe693Leu)
c.2007T>G (p.Phe669Leu)
c.1941T>G (p.Phe647Leu)
c.1884T>G (p.Phe628Leu)
15g.27926151A>GCA488959261OCA2c.2055T>C (p.Phe685=)
c.1983T>C (p.Phe661=)
c.2079T>C (p.Phe693=)
c.2007T>C (p.Phe669=)
c.1941T>C (p.Phe647=)
c.1884T>C (p.Phe628=)
15g.27926151A>TCA391360986OCA2c.2055T>A (p.Phe685Leu)
c.1983T>A (p.Phe661Leu)
c.2079T>A (p.Phe693Leu)
c.2007T>A (p.Phe669Leu)
c.1941T>A (p.Phe647Leu)
c.1884T>A (p.Phe628Leu)
15g.27926156dupCA7438784OCA2c.2055dup (p.Ala686CysfsTer?)
c.1983dup (p.Ala662CysfsTer?)
c.2079dup (p.Ala694CysfsTer?)
c.2007dup (p.Ala670CysfsTer?)
c.1941dup (p.Ala648CysfsTer?)
c.2079dup (p.Ala694CysfsTer20)
c.1884dup (p.Ala629CysfsTer?)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.27926156delCA7438783OCA2c.2055del (p.Phe685LeufsTer7)
c.1983del (p.Phe661LeufsTer7)
c.2079del (p.Phe693LeufsTer7)
c.2007del (p.Phe669LeufsTer7)
c.1941del (p.Phe647LeufsTer7)
c.1884del (p.Phe628LeufsTer7)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.27926152A>CCA391360994OCA2c.2054T>G (p.Phe685Cys)
c.1982T>G (p.Phe661Cys)
c.2078T>G (p.Phe693Cys)
c.2006T>G (p.Phe669Cys)
c.1940T>G (p.Phe647Cys)
c.1883T>G (p.Phe628Cys)

Number of alleles fetched