Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.92718814A=CA1864360927BICD2c.1831T= (p.Ser611=)
c.1912T= (p.Ser638=)
9g.92718814A>CCA374035455BICD2c.1831T>G (p.Ser611Ala)
c.1912T>G (p.Ser638Ala)
9g.92718814A>GCA5126470BICD2c.1831T>C (p.Ser611Pro)
c.1912T>C (p.Ser638Pro)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.92718814A>TCA374035460BICD2c.1831T>A (p.Ser611Thr)
c.1912T>A (p.Ser638Thr)
9g.92718815G>ACA466342991BICD2c.1830C>T (p.Gly610=)
c.1911C>T (p.Gly637=)
9g.92718815G>CCA466342993BICD2c.1830C>G (p.Gly610=)
c.1911C>G (p.Gly637=)
9g.92718815G>TCA466342992BICD2c.1830C>A (p.Gly610=)
c.1911C>A (p.Gly637=)
9g.92718816C>ACA374035464BICD2c.1829G>T (p.Gly610Val)
c.1910G>T (p.Gly637Val)
9g.92718816C>GCA374035466BICD2c.1829G>C (p.Gly610Ala)
c.1910G>C (p.Gly637Ala)
9g.92718816C>TCA374035470BICD2c.1829G>A (p.Gly610Asp)
c.1910G>A (p.Gly637Asp)
9g.92718817C>ACA374035477BICD2c.1828G>T (p.Gly610Cys)
c.1909G>T (p.Gly637Cys)
9g.92718817C>GCA374035488BICD2c.1828G>C (p.Gly610Arg)
c.1909G>C (p.Gly637Arg)
9g.92718817C>TCA374035480BICD2c.1828G>A (p.Gly610Ser)
c.1909G>A (p.Gly637Ser)
9g.92718818A>CCA466343001BICD2c.1827T>G (p.Pro609=)
c.1908T>G (p.Pro636=)
9g.92718818A>GCA466343002BICD2c.1827T>C (p.Pro609=)
c.1908T>C (p.Pro636=)
9g.92718818A>TCA466343003BICD2c.1827T>A (p.Pro609=)
c.1908T>A (p.Pro636=)
9g.92718819G>ACA374035489BICD2c.1826C>T (p.Pro609Leu)
c.1907C>T (p.Pro636Leu)
9g.92718819G>CCA374035492BICD2c.1826C>G (p.Pro609Arg)
c.1907C>G (p.Pro636Arg)
9g.92718819G>TCA374035499BICD2c.1826C>A (p.Pro609His)
c.1907C>A (p.Pro636His)
gnomAD v4
9g.92718820G>ACA374035501BICD2c.1825C>T (p.Pro609Ser)
c.1906C>T (p.Pro636Ser)
9g.92718820G>CCA374035504BICD2c.1825C>G (p.Pro609Ala)
c.1906C>G (p.Pro636Ala)
9g.92718820G>TCA374035512BICD2c.1825C>A (p.Pro609Thr)
c.1906C>A (p.Pro636Thr)
9g.92718821C>ACA466343004BICD2c.1824G>T (p.Ser608=)
c.1905G>T (p.Ser635=)
gnomAD v4
9g.92718821C=CA1864360931BICD2c.1824G= (p.Ser608=)
c.1905G= (p.Ser635=)
9g.92718821C>GCA196340036BICD2c.1824G>C (p.Ser608=)
c.1905G>C (p.Ser635=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.92718821C>TCA5126471BICD2c.1824G>A (p.Ser608=)
c.1905G>A (p.Ser635=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.92718822G>ACA5126472BICD2c.1823C>T (p.Ser608Leu)
c.1904C>T (p.Ser635Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.92718822G>CCA374035540BICD2c.1823C>G (p.Ser608Trp)
c.1904C>G (p.Ser635Trp)
9g.92718822G=CA1864360941BICD2c.1823C= (p.Ser608=)
c.1904C= (p.Ser635=)
9g.92718822G>TCA374035544BICD2c.1823C>A (p.Ser608Ter)
c.1904C>A (p.Ser635Ter)
9g.92718823A>CCA374035547BICD2c.1822T>G (p.Ser608Ala)
c.1903T>G (p.Ser635Ala)
9g.92718823A>GCA374035559BICD2c.1822T>C (p.Ser608Pro)
c.1903T>C (p.Ser635Pro)
9g.92718823A>TCA374035562BICD2c.1822T>A (p.Ser608Thr)
c.1903T>A (p.Ser635Thr)
9g.92718824G>ACA466343009BICD2c.1821C>T (p.Pro607=)
c.1902C>T (p.Pro634=)
gnomAD v4
9g.92718824G>CCA466343010BICD2c.1821C>G (p.Pro607=)
c.1902C>G (p.Pro634=)
gnomAD v4
9g.92718824G>TCA466343011BICD2c.1821C>A (p.Pro607=)
c.1902C>A (p.Pro634=)
9g.92718825G>ACA374035573BICD2c.1820C>T (p.Pro607Leu)
c.1901C>T (p.Pro634Leu)
9g.92718825G>CCA374035571BICD2c.1820C>G (p.Pro607Arg)
c.1901C>G (p.Pro634Arg)
gnomAD v4
9g.92718825G>TCA374035568BICD2c.1820C>A (p.Pro607His)
c.1901C>A (p.Pro634His)
9g.92718826G>ACA374035576BICD2c.1819C>T (p.Pro607Ser)
c.1900C>T (p.Pro634Ser)
gnomAD v4
9g.92718826G>CCA374035577BICD2c.1819C>G (p.Pro607Ala)
c.1900C>G (p.Pro634Ala)
dbSNP gnomAD v4
9g.92718826G=CA1864360950BICD2c.1819C= (p.Pro607=)
c.1900C= (p.Pro634=)
9g.92718826G>TCA374035578BICD2c.1819C>A (p.Pro607Thr)
c.1900C>A (p.Pro634Thr)
9g.92718827G>ACA466343014BICD2c.1818C>T (p.Ser606=)
c.1899C>T (p.Ser633=)
9g.92718827G>CCA374035579BICD2c.1818C>G (p.Ser606Arg)
c.1899C>G (p.Ser633Arg)
9g.92718827G>TCA374035581BICD2c.1818C>A (p.Ser606Arg)
c.1899C>A (p.Ser633Arg)
gnomAD v4
9g.92718828C>ACA374035584BICD2c.1817G>T (p.Ser606Ile)
c.1898G>T (p.Ser633Ile)
9g.92718828C=CA1864360954BICD2c.1817G= (p.Ser606=)
c.1898G= (p.Ser633=)
9g.92718828C>GCA374035587BICD2c.1817G>C (p.Ser606Thr)
c.1898G>C (p.Ser633Thr)
9g.92718828C>TCA196340065BICD2c.1817G>A (p.Ser606Asn)
c.1898G>A (p.Ser633Asn)
ClinVar dbSNP gnomAD v4

Number of alleles fetched