Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107701928_107701929delCA4432978SLC26A4c.1905_1906del (p.Glu635AspfsTer8)
c.616_617del
n.192_193del
c.1827_1828del (p.Glu609AspfsTer8)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107701928G>ACA4432980SLC26A4c.1905G>A (p.Glu635=)
c.616G>A
n.192G>A
c.1827G>A (p.Glu609=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107701928G>CCA368843492SLC26A4c.1905G>C (p.Glu635Asp)
c.616G>C
n.192G>C
c.1827G>C (p.Glu609Asp)
 dbSNP gnomAD v3 gnomAD v4
7g.107701928G=CA1732759228SLC26A4c.1905G= (p.Glu635=)
c.616G=
n.192G=
c.1827G= (p.Glu609=)
7g.107701928G>TCA368843494SLC26A4c.1905G>T (p.Glu635Asp)
c.616G>T
n.192G>T
c.1827G>T (p.Glu609Asp)
7g.107701929A=CA1732759233SLC26A4c.1906A= (p.Ile636=)
c.617A=
n.193A=
c.1828A= (p.Ile610=)
7g.107701929A>CCA368843496SLC26A4c.1906A>C (p.Ile636Leu)
c.617A>C
n.193A>C
c.1828A>C (p.Ile610Leu)
7g.107701929A>GCA4432981SLC26A4c.1906A>G (p.Ile636Val)
c.617A>G
n.193A>G
c.1828A>G (p.Ile610Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107701929A>TCA368843498SLC26A4c.1906A>T (p.Ile636Phe)
c.617A>T
n.193A>T
c.1828A>T (p.Ile610Phe)
7g.107701930T>ACA368843500SLC26A4c.1907T>A (p.Ile636Asn)
c.618T>A
n.194T>A
c.1829T>A (p.Ile610Asn)
7g.107701930T>CCA368843502SLC26A4c.1907T>C (p.Ile636Thr)
c.618T>C
n.194T>C
c.1829T>C (p.Ile610Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.107701930T>GCA368843503SLC26A4c.1907T>G (p.Ile636Ser)
c.618T>G
n.194T>G
c.1829T>G (p.Ile610Ser)
 gnomAD v4
7g.107701930T=CA1732759239SLC26A4c.1907T= (p.Ile636=)
c.618T=
n.194T=
c.1829T= (p.Ile610=)
7g.107701931T>ACA457103252SLC26A4c.1908T>A (p.Ile636=)
c.619T>A
n.195T>A
c.1830T>A (p.Ile610=)
 gnomAD v4
7g.107701931T>CCA457103253SLC26A4c.1908T>C (p.Ile636=)
c.619T>C
n.195T>C
c.1830T>C (p.Ile610=)
7g.107701931T>GCA368843505SLC26A4c.1908T>G (p.Ile636Met)
c.619T>G
n.195T>G
c.1830T>G (p.Ile610Met)
7g.107701932C>ACA4432982SLC26A4c.1909C>A (p.Gln637Lys)
c.620C>A
n.196C>A
c.1831C>A (p.Gln611Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107701932C=CA1732759243SLC26A4c.1909C= (p.Gln637=)
c.620C=
n.196C=
c.1831C= (p.Gln611=)
7g.107701932C>GCA368843508SLC26A4c.1909C>G (p.Gln637Glu)
c.620C>G
n.196C>G
c.1831C>G (p.Gln611Glu)
7g.107701932C>TCA368843510SLC26A4c.1909C>T (p.Gln637Ter)
c.620C>T
n.196C>T
c.1831C>T (p.Gln611Ter)
7g.107701933A>CCA368843514SLC26A4c.1910A>C (p.Gln637Pro)
c.621A>C
n.197A>C
c.1832A>C (p.Gln611Pro)
7g.107701933A>GCA368843513SLC26A4c.1910A>G (p.Gln637Arg)
c.621A>G
n.197A>G
c.1832A>G (p.Gln611Arg)
7g.107701933A>TCA368843511SLC26A4c.1910A>T (p.Gln637Leu)
c.621A>T
n.197A>T
c.1832A>T (p.Gln611Leu)
7g.107701934A>CCA368843518SLC26A4c.1911A>C (p.Gln637His)
c.622A>C
n.198A>C
c.1833A>C (p.Gln611His)
7g.107701934A>GCA457103254SLC26A4c.1911A>G (p.Gln637=)
c.622A>G
n.198A>G
c.1833A>G (p.Gln611=)
7g.107701934A>TCA368843516SLC26A4c.1911A>T (p.Gln637His)
c.622A>T
n.198A>T
c.1833A>T (p.Gln611His)
7g.107701935G>ACA368843520SLC26A4c.1912G>A (p.Val638Met)
c.623G>A
n.199G>A
c.1834G>A (p.Val612Met)
7g.107701935G>CCA368843522SLC26A4c.1912G>C (p.Val638Leu)
c.623G>C
n.199G>C
c.1834G>C (p.Val612Leu)
7g.107701935G>TCA368843524SLC26A4c.1912G>T (p.Val638Leu)
c.623G>T
n.199G>T
c.1834G>T (p.Val612Leu)
7g.107701936T>ACA368843525SLC26A4c.1913T>A (p.Val638Glu)
c.624T>A
n.200T>A
c.1835T>A (p.Val612Glu)
7g.107701936T>CCA368843527SLC26A4c.1913T>C (p.Val638Ala)
c.624T>C
n.200T>C
c.1835T>C (p.Val612Ala)
7g.107701936T>GCA368843529SLC26A4c.1913T>G (p.Val638Gly)
c.624T>G
n.200T>G
c.1835T>G (p.Val612Gly)
7g.107701937G>ACA457103257SLC26A4c.1914G>A (p.Val638=)
c.625G>A
n.201G>A
c.1836G>A (p.Val612=)
7g.107701937G>CCA457103256SLC26A4c.1914G>C (p.Val638=)
c.625G>C
n.201G>C
c.1836G>C (p.Val612=)
7g.107701937G>TCA457103255SLC26A4c.1914G>T (p.Val638=)
c.625G>T
n.201G>T
c.1836G>T (p.Val612=)
7g.107701938G>ACA368843531SLC26A4c.1915G>A (p.Asp639Asn)
c.626G>A
n.202G>A
c.1837G>A (p.Asp613Asn)
7g.107701938G>CCA4432983SLC26A4c.1915G>C (p.Asp639His)
c.626G>C
n.202G>C
c.1837G>C (p.Asp613His)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107701938G=CA1732759250SLC26A4c.1915G= (p.Asp639=)
c.626G=
n.202G=
c.1837G= (p.Asp613=)
7g.107701938G>TCA4432984SLC26A4c.1915G>T (p.Asp639Tyr)
c.626G>T
n.202G>T
c.1837G>T (p.Asp613Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.107701939A>CCA368843534SLC26A4c.1916A>C (p.Asp639Ala)
c.627A>C
n.203A>C
c.1838A>C (p.Asp613Ala)
7g.107701939A>GCA368843535SLC26A4c.1916A>G (p.Asp639Gly)
c.627A>G
n.203A>G
c.1838A>G (p.Asp613Gly)
 dbSNP
7g.107701939A>TCA368843537SLC26A4c.1916A>T (p.Asp639Val)
c.627A>T
n.203A>T
c.1838A>T (p.Asp613Val)
7g.107701940T>ACA368843540SLC26A4c.1917T>A (p.Asp639Glu)
c.628T>A
n.204T>A
c.1839T>A (p.Asp613Glu)
7g.107701940T>CCA4432985SLC26A4c.1917T>C (p.Asp639=)
c.628T>C
n.204T>C
c.1839T>C (p.Asp613=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.107701940T>GCA368843539SLC26A4c.1917T>G (p.Asp639Glu)
c.628T>G
n.204T>G
c.1839T>G (p.Asp613Glu)
7g.107701940T=CA1732759255SLC26A4c.1917T= (p.Asp639=)
c.628T=
n.204T=
c.1839T= (p.Asp613=)
7g.107701941T>ACA368843542SLC26A4c.1918T>A (p.Trp640Arg)
c.629T>A
n.205T>A
c.1840T>A (p.Trp614Arg)
7g.107701941T>CCA164218559SLC26A4c.1918T>C (p.Trp640Arg)
c.629T>C
n.205T>C
c.1840T>C (p.Trp614Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.107701941T>GCA368843544SLC26A4c.1918T>G (p.Trp640Gly)
c.629T>G
n.205T>G
c.1840T>G (p.Trp614Gly)
 gnomAD v4
7g.107701941T=CA1732759259SLC26A4c.1918T= (p.Trp640=)
c.629T=
n.205T=
c.1840T= (p.Trp614=)
7g.107701942G>ACA274015SLC26A4c.1919G>A (p.Trp640Ter)
c.630G>A
n.206G>A
c.1841G>A (p.Trp614Ter)
 ClinVar dbSNP gnomAD v4
7g.107701942G>CCA368843547SLC26A4c.1919G>C (p.Trp640Ser)
c.630G>C
n.206G>C
c.1841G>C (p.Trp614Ser)
7g.107701942G=CA1732759266SLC26A4c.1919G= (p.Trp640=)
c.630G=
n.206G=
c.1841G= (p.Trp614=)
7g.107701942G>TCA368843549SLC26A4c.1919G>T (p.Trp640Leu)
c.630G>T
n.206G>T
c.1841G>T (p.Trp614Leu)
 dbSNP gnomAD v4
7g.107701943G>ACA274264SLC26A4c.1920G>A (p.Trp640Ter)
c.631G>A
n.207G>A
c.1842G>A (p.Trp614Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.107701943G>CCA4432986SLC26A4c.1920G>C (p.Trp640Cys)
c.631G>C
n.207G>C
c.1842G>C (p.Trp614Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107701943G=CA1732759280SLC26A4c.1920G= (p.Trp640=)
c.631G=
n.207G=
c.1842G= (p.Trp614=)
7g.107701943G>TCA368843552SLC26A4c.1920G>T (p.Trp640Cys)
c.631G>T
n.207G>T
c.1842G>T (p.Trp614Cys)
 dbSNP
7g.107701943_107701944delinsGACA1732759278SLC26A4c.1920_1921delinsGA (p.Trp640=)
c.631_632delinsGA
n.207_208delinsGA
c.1842_1843delinsGA (p.Trp614=)
7g.107701944A>CCA368843554SLC26A4c.1921A>C (p.Asn641His)
c.632A>C
n.208A>C
c.1843A>C (p.Asn615His)
7g.107701944A>GCA368843556SLC26A4c.1921A>G (p.Asn641Asp)
c.632A>G
n.208A>G
c.1843A>G (p.Asn615Asp)
7g.107701944A>TCA368843558SLC26A4c.1921A>T (p.Asn641Tyr)
c.632A>T
n.208A>T
c.1843A>T (p.Asn615Tyr)
7g.107701945delCA915945414SLC26A4c.1922del (p.Asn641ThrfsTer8)
c.633del
n.209del
c.1844del (p.Asn615ThrfsTer8)
 ClinVar dbSNP
7g.107701945A=CA1732759293SLC26A4c.1922A= (p.Asn641=)
c.633A=
n.209A=
c.1844A= (p.Asn615=)
7g.107701945A>CCA368843563SLC26A4c.1922A>C (p.Asn641Thr)
c.633A>C
n.209A>C
c.1844A>C (p.Asn615Thr)
7g.107701945A>GCA4432987SLC26A4c.1922A>G (p.Asn641Ser)
c.633A>G
n.209A>G
c.1844A>G (p.Asn615Ser)
 dbSNP ExAC gnomAD v2
7g.107701945A>TCA368843560SLC26A4c.1922A>T (p.Asn641Ile)
c.633A>T
n.209A>T
c.1844A>T (p.Asn615Ile)
7g.107701946C>ACA368843564SLC26A4c.1923C>A (p.Asn641Lys)
c.634C>A
n.210C>A
c.1845C>A (p.Asn615Lys)
7g.107701946C=CA1732759299SLC26A4c.1923C= (p.Asn641=)
c.634C=
n.210C=
c.1845C= (p.Asn615=)
7g.107701946C>GCA368843566SLC26A4c.1923C>G (p.Asn641Lys)
c.634C>G
n.210C>G
c.1845C>G (p.Asn615Lys)
7g.107701946C>TCA457103258SLC26A4c.1923C>T (p.Asn641=)
c.634C>T
n.210C>T
c.1845C>T (p.Asn615=)
 ClinVar dbSNP gnomAD v4
7g.107701947T>ACA368843567SLC26A4c.1924T>A (p.Ser642Thr)
c.635T>A
n.211T>A
c.1846T>A (p.Ser616Thr)
7g.107701947T>CCA132685SLC26A4c.1924T>C (p.Ser642Pro)
c.635T>C
n.211T>C
c.1846T>C (p.Ser616Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107701947T>GCA368843570SLC26A4c.1924T>G (p.Ser642Ala)
c.635T>G
n.211T>G
c.1846T>G (p.Ser616Ala)
7g.107701947T=CA1732759305SLC26A4c.1924T= (p.Ser642=)
c.635T=
n.211T=
c.1846T= (p.Ser616=)
7g.107701947_107701948insTTGAAGATCA2684467832SLC26A4c.1924_1925insTTGAAGAT (p.Ser642PhefsTer10)
c.635_636insTTGAAGAT
n.211_212insTTGAAGAT
c.1846_1847insTTGAAGAT (p.Ser616PhefsTer10)
 gnomAD v4
7g.107701948C>ACA368843571SLC26A4c.1925C>A (p.Ser642Tyr)
c.636C>A
n.212C>A
c.1847C>A (p.Ser616Tyr)
 COSMIC
7g.107701948C>GCA368843573SLC26A4c.1925C>G (p.Ser642Cys)
c.636C>G
n.212C>G
c.1847C>G (p.Ser616Cys)
7g.107701948C>TCA368843575SLC26A4c.1925C>T (p.Ser642Phe)
c.636C>T
n.212C>T
c.1847C>T (p.Ser616Phe)
7g.107701949T>ACA457103259SLC26A4c.1926T>A (p.Ser642=)
c.637T>A
n.213T>A
c.1848T>A (p.Ser616=)
7g.107701949T>CCA457103260SLC26A4c.1926T>C (p.Ser642=)
c.637T>C
n.213T>C
c.1848T>C (p.Ser616=)
7g.107701949T>GCA457103261SLC26A4c.1926T>G (p.Ser642=)
c.637T>G
n.213T>G
c.1848T>G (p.Ser616=)
 ClinVar gnomAD v4
7g.107701950G>ACA368843577SLC26A4c.1927G>A (p.Glu643Lys)
c.638G>A
n.214G>A
c.1849G>A (p.Glu617Lys)
 gnomAD v4
7g.107701950G>CCA368843578SLC26A4c.1927G>C (p.Glu643Gln)
c.638G>C
n.214G>C
c.1849G>C (p.Glu617Gln)
 COSMIC COSMIC
7g.107701950G>TCA368843580SLC26A4c.1927G>T (p.Glu643Ter)
c.638G>T
n.214G>T
c.1849G>T (p.Glu617Ter)
7g.107701950_107701951insGAGGAACTTGATATCCCAACCAAGGAAATAGAGATTCAAGTGGATTGGCA2684467833SLC26A4c.1927_1928insGAGGAACTTGATATCCCAACCAAGGAAATAGAGATTCAAGTGGATTGG (p.Glu643GlyfsTer4)
c.638_639insGAGGAACTTGATATCCCAACCAAGGAAATAGAGATTCAAGTGGATTGG
n.214_215insGAGGAACTTGATATCCCAACCAAGGAAATAGAGATTCAAGTGGATTGG
c.1849_1850insGAGGAACTTGATATCCCAACCAAGGAAATAGAGATTCAAGTGGATTGG (p.Glu617GlyfsTer4)
 gnomAD v4
7g.107701951A>CCA368843582SLC26A4c.1928A>C (p.Glu643Ala)
c.639A>C
n.215A>C
c.1850A>C (p.Glu617Ala)
 gnomAD v4
7g.107701951A>GCA368843584SLC26A4c.1928A>G (p.Glu643Gly)
c.639A>G
n.215A>G
c.1850A>G (p.Glu617Gly)
7g.107701951A>TCA368843585SLC26A4c.1928A>T (p.Glu643Val)
c.639A>T
n.215A>T
c.1850A>T (p.Glu617Val)
7g.107701952G>ACA457103262SLC26A4c.1929G>A (p.Glu643=)
c.640G>A
n.216G>A
c.1851G>A (p.Glu617=)
7g.107701952G>CCA368843587SLC26A4c.1929G>C (p.Glu643Asp)
c.640G>C
n.216G>C
c.1851G>C (p.Glu617Asp)
7g.107701952G>TCA368843586SLC26A4c.1929G>T (p.Glu643Asp)
c.640G>T
n.216G>T
c.1851G>T (p.Glu617Asp)
7g.107701953C>ACA368843590SLC26A4c.1930C>A (p.Leu644Ile)
c.641C>A
n.217C>A
c.1852C>A (p.Leu618Ile)
7g.107701953C>GCA368843592SLC26A4c.1930C>G (p.Leu644Val)
c.641C>G
n.217C>G
c.1852C>G (p.Leu618Val)
7g.107701953C>TCA368843593SLC26A4c.1930C>T (p.Leu644Phe)
c.641C>T
n.217C>T
c.1852C>T (p.Leu618Phe)
7g.107701954T>ACA368843595SLC26A4c.1931T>A (p.Leu644His)
c.642T>A
n.218T>A
c.1853T>A (p.Leu618His)
7g.107701954T>CCA368843597SLC26A4c.1931T>C (p.Leu644Pro)
c.642T>C
n.218T>C
c.1853T>C (p.Leu618Pro)
 gnomAD v4
7g.107701954T>GCA368843599SLC26A4c.1931T>G (p.Leu644Arg)
c.642T>G
n.218T>G
c.1853T>G (p.Leu618Arg)
7g.107701955T>ACA457103263SLC26A4c.1932T>A (p.Leu644=)
c.643T>A
n.219T>A
c.1854T>A (p.Leu618=)
7g.107701955T>CCA457103265SLC26A4c.1932T>C (p.Leu644=)
c.643T>C
n.219T>C
c.1854T>C (p.Leu618=)
 ClinVar
7g.107701955T>GCA457103264SLC26A4c.1932T>G (p.Leu644=)
c.643T>G
n.219T>G
c.1854T>G (p.Leu618=)
7g.107701956C>ACA368843600SLC26A4c.1933C>A (p.Pro645Thr)
c.644C>A
n.220C>A
c.1855C>A (p.Pro619Thr)
7g.107701956C>GCA368843602SLC26A4c.1933C>G (p.Pro645Ala)
c.644C>G
n.220C>G
c.1855C>G (p.Pro619Ala)
7g.107701956C>TCA368843603SLC26A4c.1933C>T (p.Pro645Ser)
c.644C>T
n.220C>T
c.1855C>T (p.Pro619Ser)
7g.107701957C>ACA368843606SLC26A4c.1934C>A (p.Pro645Gln)
c.645C>A
n.221C>A
c.1856C>A (p.Pro619Gln)
7g.107701957C>GCA368843608SLC26A4c.1934C>G (p.Pro645Arg)
c.645C>G
n.221C>G
c.1856C>G (p.Pro619Arg)
7g.107701957C>TCA368843609SLC26A4c.1934C>T (p.Pro645Leu)
c.645C>T
n.221C>T
c.1856C>T (p.Pro619Leu)
7g.107701958A=CA1732759314SLC26A4c.1935A= (p.Pro645=)
c.646A=
n.222A=
c.1857A= (p.Pro619=)
7g.107701958A>CCA164218575SLC26A4c.1935A>C (p.Pro645=)
c.646A>C
n.222A>C
c.1857A>C (p.Pro619=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.107701958A>GCA457103266SLC26A4c.1935A>G (p.Pro645=)
c.646A>G
n.222A>G
c.1857A>G (p.Pro619=)
 dbSNP gnomAD v2 gnomAD v4
7g.107701958A>TCA457103267SLC26A4c.1935A>T (p.Pro645=)
c.646A>T
n.222A>T
c.1857A>T (p.Pro619=)
 gnomAD v4
7g.107701959G>ACA368843615SLC26A4c.1936G>A (p.Val646Ile)
c.647G>A
n.223G>A
c.1858G>A (p.Val620Ile)
 dbSNP gnomAD v3 gnomAD v4
7g.107701959G>CCA368843613SLC26A4c.1936G>C (p.Val646Leu)
c.647G>C
n.223G>C
c.1858G>C (p.Val620Leu)
7g.107701959G=CA1732759320SLC26A4c.1936G= (p.Val646=)
c.647G=
n.223G=
c.1858G= (p.Val620=)
7g.107701959G>TCA368843611SLC26A4c.1936G>T (p.Val646Phe)
c.647G>T
n.223G>T
c.1858G>T (p.Val620Phe)
7g.107701960T>ACA368843620SLC26A4c.1937T>A (p.Val646Asp)
c.648T>A
n.224T>A
c.1859T>A (p.Val620Asp)
7g.107701960T>CCA368843617SLC26A4c.1937T>C (p.Val646Ala)
c.648T>C
n.224T>C
c.1859T>C (p.Val620Ala)
7g.107701960T>GCA368843619SLC26A4c.1937T>G (p.Val646Gly)
c.648T>G
n.224T>G
c.1859T>G (p.Val620Gly)
 dbSNP
7g.107701960T=CA1732759323SLC26A4c.1937T= (p.Val646=)
c.648T=
n.224T=
c.1859T= (p.Val620=)
7g.107701961C>ACA457103268SLC26A4c.1938C>A (p.Val646=)
c.649C>A
n.225C>A
c.1860C>A (p.Val620=)
7g.107701961C>GCA457103270SLC26A4c.1938C>G (p.Val646=)
c.649C>G
n.225C>G
c.1860C>G (p.Val620=)
 COSMIC
7g.107701961C>TCA457103269SLC26A4c.1938C>T (p.Val646=)
c.649C>T
n.225C>T
c.1860C>T (p.Val620=)
7g.107701962A>CCA368843622SLC26A4c.1939A>C (p.Lys647Gln)
c.650A>C
n.226A>C
c.1861A>C (p.Lys621Gln)
7g.107701962A>GCA368843624SLC26A4c.1939A>G (p.Lys647Glu)
c.650A>G
n.226A>G
c.1861A>G (p.Lys621Glu)
7g.107701962A>TCA368843625SLC26A4c.1939A>T (p.Lys647Ter)
c.650A>T
n.226A>T
c.1861A>T (p.Lys621Ter)
7g.107701963A>CCA368843626SLC26A4c.1940A>C (p.Lys647Thr)
c.651A>C
n.227A>C
c.1862A>C (p.Lys621Thr)
7g.107701963A>GCA368843628SLC26A4c.1940A>G (p.Lys647Arg)
c.651A>G
n.227A>G
c.1862A>G (p.Lys621Arg)
7g.107701963A>TCA368843629SLC26A4c.1940A>T (p.Lys647Ile)
c.651A>T
n.227A>T
c.1862A>T (p.Lys621Ile)
7g.107701964A>CCA368843630SLC26A4c.1941A>C (p.Lys647Asn)
c.652A>C
n.228A>C
c.1863A>C (p.Lys621Asn)
7g.107701964A>GCA457103273SLC26A4c.1941A>G (p.Lys647=)
c.652A>G
n.228A>G
c.1863A>G (p.Lys621=)
7g.107701964A>TCA368843632SLC26A4c.1941A>T (p.Lys647Asn)
c.652A>T
n.228A>T
c.1863A>T (p.Lys621Asn)
7g.107701965G>ACA368843634SLC26A4c.1942G>A (p.Val648Met)
c.653G>A
n.229G>A
c.1864G>A (p.Val622Met)
7g.107701965G>CCA368843636SLC26A4c.1942G>C (p.Val648Leu)
c.653G>C
n.229G>C
c.1864G>C (p.Val622Leu)
7g.107701965G>TCA368843638SLC26A4c.1942G>T (p.Val648Leu)
c.653G>T
n.229G>T
c.1864G>T (p.Val622Leu)
7g.107701966T>ACA368843643SLC26A4c.1943T>A (p.Val648Glu)
c.654T>A
n.230T>A
c.1865T>A (p.Val622Glu)
7g.107701966T>CCA368843640SLC26A4c.1943T>C (p.Val648Ala)
c.654T>C
n.230T>C
c.1865T>C (p.Val622Ala)
7g.107701966T>GCA368843641SLC26A4c.1943T>G (p.Val648Gly)
c.654T>G
n.230T>G
c.1865T>G (p.Val622Gly)
7g.107701967G>ACA457103290SLC26A4c.1944G>A (p.Val648=)
c.655G>A
n.231G>A
c.1866G>A (p.Val622=)
7g.107701967G>CCA457103293SLC26A4c.1944G>C (p.Val648=)
c.655G>C
n.231G>C
c.1866G>C (p.Val622=)
 gnomAD v4
7g.107701967G>TCA457103294SLC26A4c.1944G>T (p.Val648=)
c.655G>T
n.231G>T
c.1866G>T (p.Val622=)
7g.107701968A>CCA368843645SLC26A4c.1945A>C (p.Asn649His)
c.656A>C
n.232A>C
c.1867A>C (p.Asn623His)
7g.107701968A>GCA368843647SLC26A4c.1945A>G (p.Asn649Asp)
c.656A>G
n.232A>G
c.1867A>G (p.Asn623Asp)
 gnomAD v4
7g.107701968A>TCA368843648SLC26A4c.1945A>T (p.Asn649Tyr)
c.656A>T
n.232A>T
c.1867A>T (p.Asn623Tyr)
7g.107701969A>CCA368843650SLC26A4c.1946A>C (p.Asn649Thr)
c.657A>C
n.233A>C
c.1868A>C (p.Asn623Thr)
7g.107701969A>GCA368843652SLC26A4c.1946A>G (p.Asn649Ser)
c.657A>G
n.233A>G
c.1868A>G (p.Asn623Ser)
7g.107701969A>TCA368843654SLC26A4c.1946A>T (p.Asn649Ile)
c.657A>T
n.233A>T
c.1868A>T (p.Asn623Ile)
7g.107701970C>ACA164218579SLC26A4c.1947C>A (p.Asn649Lys)
c.658C>A
n.234C>A
c.1869C>A (p.Asn623Lys)
 dbSNP gnomAD v4
7g.107701970C=CA1732759327SLC26A4c.1947C= (p.Asn649=)
c.658C=
n.234C=
c.1869C= (p.Asn623=)
7g.107701970C>GCA368843655SLC26A4c.1947C>G (p.Asn649Lys)
c.658C>G
n.234C>G
c.1869C>G (p.Asn623Lys)
7g.107701970C>TCA4432988SLC26A4c.1947C>T (p.Asn649=)
c.658C>T
n.234C>T
c.1869C>T (p.Asn623=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107701971G>ACA4432989SLC26A4c.1948G>A (p.Val650Ile)
c.659G>A
n.235G>A
c.1870G>A (p.Val624Ile)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107701971G>CCA368843658SLC26A4c.1948G>C (p.Val650Leu)
c.659G>C
n.235G>C
c.1870G>C (p.Val624Leu)
7g.107701971G=CA1732759336SLC26A4c.1948G= (p.Val650=)
c.659G=
n.235G=
c.1870G= (p.Val624=)
7g.107701971G>TCA368843660SLC26A4c.1948G>T (p.Val650Phe)
c.659G>T
n.235G>T
c.1870G>T (p.Val624Phe)
7g.107701972T>ACA16041115SLC26A4c.1949T>A (p.Val650Asp)
c.660T>A
n.236T>A
c.1871T>A (p.Val624Asp)
 ClinVar dbSNP
7g.107701972T>CCA368843664SLC26A4c.1949T>C (p.Val650Ala)
c.660T>C
n.236T>C
c.1871T>C (p.Val624Ala)
 gnomAD v4
7g.107701972T>GCA368843662SLC26A4c.1949T>G (p.Val650Gly)
c.660T>G
n.236T>G
c.1871T>G (p.Val624Gly)
7g.107701972T=CA1732759343SLC26A4c.1949T= (p.Val650=)
c.660T=
n.236T=
c.1871T= (p.Val624=)
7g.107701973T>ACA457103325SLC26A4c.1950T>A (p.Val650=)
c.661T>A
n.237T>A
c.1872T>A (p.Val624=)
7g.107701973T>CCA457103327SLC26A4c.1950T>C (p.Val650=)
c.661T>C
n.237T>C
c.1872T>C (p.Val624=)
 ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
7g.107701973T>GCA457103330SLC26A4c.1950T>G (p.Val650=)
c.661T>G
n.237T>G
c.1872T>G (p.Val624=)
7g.107701973T=CA1732759349SLC26A4c.1950T= (p.Val650=)
c.661T=
n.237T=
c.1872T= (p.Val624=)
7g.107701974C>ACA368843665SLC26A4c.1951C>A (p.Pro651Thr)
c.662C>A
n.238C>A
c.1873C>A (p.Pro625Thr)
7g.107701974C>GCA368843667SLC26A4c.1951C>G (p.Pro651Ala)
c.662C>G
n.238C>G
c.1873C>G (p.Pro625Ala)
7g.107701974C>TCA368843666SLC26A4c.1951C>T (p.Pro651Ser)
c.662C>T
n.238C>T
c.1873C>T (p.Pro625Ser)
 gnomAD v4
7g.107701975C>ACA368843669SLC26A4c.1952C>A (p.Pro651His)
c.663C>A
n.239C>A
c.1874C>A (p.Pro625His)
7g.107701975C>GCA368843670SLC26A4c.1952C>G (p.Pro651Arg)
c.663C>G
n.239C>G
c.1874C>G (p.Pro625Arg)
7g.107701975C>TCA368843672SLC26A4c.1952C>T (p.Pro651Leu)
c.663C>T
n.239C>T
c.1874C>T (p.Pro625Leu)
 gnomAD v4
7g.107701976C>ACA457103346SLC26A4c.1953C>A (p.Pro651=)
c.664C>A
n.240C>A
c.1875C>A (p.Pro625=)
7g.107701976C=CA1732759352SLC26A4c.1953C= (p.Pro651=)
c.664C=
n.240C=
c.1875C= (p.Pro625=)
7g.107701976C>GCA457103343SLC26A4c.1953C>G (p.Pro651=)
c.664C>G
n.240C>G
c.1875C>G (p.Pro625=)
7g.107701976C>TCA457103349SLC26A4c.1953C>T (p.Pro651=)
c.664C>T
n.240C>T
c.1875C>T (p.Pro625=)
 dbSNP gnomAD v3 gnomAD v4
7g.107701977A>CCA368843674SLC26A4c.1954A>C (p.Lys652Gln)
c.665A>C
n.241A>C
c.1876A>C (p.Lys626Gln)
7g.107701977A>GCA368843675SLC26A4c.1954A>G (p.Lys652Glu)
c.665A>G
n.241A>G
c.1876A>G (p.Lys626Glu)
7g.107701977A>TCA368843677SLC26A4c.1954A>T (p.Lys652Ter)
c.665A>T
n.241A>T
c.1876A>T (p.Lys626Ter)
7g.107701979delCA2684467835SLC26A4c.1956del (p.Val653CysfsTer21)
c.667del
n.243del
c.1878del (p.Val627CysfsTer21)
 gnomAD v4
7g.107701978A=CA1732759355SLC26A4c.1955A= (p.Lys652=)
c.666A=
n.242A=
c.1877A= (p.Lys626=)
7g.107701978A>CCA368843681SLC26A4c.1955A>C (p.Lys652Thr)
c.666A>C
n.242A>C
c.1877A>C (p.Lys626Thr)
7g.107701978A>GCA4432990SLC26A4c.1955A>G (p.Lys652Arg)
c.666A>G
n.242A>G
c.1877A>G (p.Lys626Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.107701978A>TCA368843680SLC26A4c.1955A>T (p.Lys652Ile)
c.666A>T
n.242A>T
c.1877A>T (p.Lys626Ile)
7g.107701979A>CCA368843683SLC26A4c.1956A>C (p.Lys652Asn)
c.667A>C
n.243A>C
c.1878A>C (p.Lys626Asn)
7g.107701979A>GCA457103375SLC26A4c.1956A>G (p.Lys652=)
c.667A>G
n.243A>G
c.1878A>G (p.Lys626=)
 gnomAD v4
7g.107701979A>TCA368843684SLC26A4c.1956A>T (p.Lys652Asn)
c.667A>T
n.243A>T
c.1878A>T (p.Lys626Asn)
 COSMIC
7g.107701980G>ACA368843685SLC26A4c.1957G>A (p.Val653Met)
c.668G>A
n.244G>A
c.1879G>A (p.Val627Met)
7g.107701980G>CCA368843687SLC26A4c.1957G>C (p.Val653Leu)
c.668G>C
n.244G>C
c.1879G>C (p.Val627Leu)
 ClinVar dbSNP gnomAD v4
7g.107701980G=CA1732759361SLC26A4c.1957G= (p.Val653=)
c.668G=
n.244G=
c.1879G= (p.Val627=)
7g.107701980G>TCA368843689SLC26A4c.1957G>T (p.Val653Leu)
c.668G>T
n.244G>T
c.1879G>T (p.Val627Leu)
7g.107701981T>ACA368843695SLC26A4c.1958T>A (p.Val653Glu)
c.669T>A
n.245T>A
c.1880T>A (p.Val627Glu)
7g.107701981T>CCA368843691SLC26A4c.1958T>C (p.Val653Ala)
c.669T>C
n.245T>C
c.1880T>C (p.Val627Ala)
 ClinVar dbSNP gnomAD v4
7g.107701981T>GCA368843693SLC26A4c.1958T>G (p.Val653Gly)
c.669T>G
n.245T>G
c.1880T>G (p.Val627Gly)
7g.107701981T=CA1732759371SLC26A4c.1958T= (p.Val653=)
c.669T=
n.245T=
c.1880T= (p.Val627=)
7g.107701982G>ACA457103394SLC26A4c.1959G>A (p.Val653=)
c.670G>A
n.246G>A
c.1881G>A (p.Val627=)
7g.107701982G>CCA457103396SLC26A4c.1959G>C (p.Val653=)
c.670G>C
n.246G>C
c.1881G>C (p.Val627=)
7g.107701982G>TCA457103398SLC26A4c.1959G>T (p.Val653=)
c.670G>T
n.246G>T
c.1881G>T (p.Val627=)
7g.107701983C>ACA368843696SLC26A4c.1960C>A (p.Pro654Thr)
c.671C>A
n.247C>A
c.1882C>A (p.Pro628Thr)
7g.107701983C=CA1732759378SLC26A4c.1960C= (p.Pro654=)
c.671C=
n.247C=
c.1882C= (p.Pro628=)
7g.107701983C>GCA368843698SLC26A4c.1960C>G (p.Pro654Ala)
c.671C>G
n.247C>G
c.1882C>G (p.Pro628Ala)
7g.107701983C>TCA368843700SLC26A4c.1960C>T (p.Pro654Ser)
c.671C>T
n.247C>T
c.1882C>T (p.Pro628Ser)
 dbSNP gnomAD v4
7g.107701984C>ACA368843702SLC26A4c.1961C>A (p.Pro654Gln)
c.672C>A
n.248C>A
c.1883C>A (p.Pro628Gln)
7g.107701984C>GCA368843703SLC26A4c.1961C>G (p.Pro654Arg)
c.672C>G
n.248C>G
c.1883C>G (p.Pro628Arg)
7g.107701984C>TCA368843705SLC26A4c.1961C>T (p.Pro654Leu)
c.672C>T
n.248C>T
c.1883C>T (p.Pro628Leu)
 gnomAD v4 COSMIC
7g.107701985A>CCA457103415SLC26A4c.1962A>C (p.Pro654=)
c.673A>C
n.249A>C
c.1884A>C (p.Pro628=)
7g.107701985A>GCA457103418SLC26A4c.1962A>G (p.Pro654=)
c.673A>G
n.249A>G
c.1884A>G (p.Pro628=)
 ClinVar
7g.107701985A>TCA457103421SLC26A4c.1962A>T (p.Pro654=)
c.673A>T
n.249A>T
c.1884A>T (p.Pro628=)
7g.107701986A=CA1732759383SLC26A4c.1963A= (p.Ile655=)
c.674A=
n.250A=
c.1885A= (p.Ile629=)
7g.107701986A>CCA368843707SLC26A4c.1963A>C (p.Ile655Leu)
c.674A>C
n.250A>C
c.1885A>C (p.Ile629Leu)
7g.107701986A>GCA261421SLC26A4c.1963A>G (p.Ile655Val)
c.674A>G
n.250A>G
c.1885A>G (p.Ile629Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107701986A>TCA368843709SLC26A4c.1963A>T (p.Ile655Phe)
c.674A>T
n.250A>T
c.1885A>T (p.Ile629Phe)
7g.107701987T>ACA368843711SLC26A4c.1964T>A (p.Ile655Asn)
c.675T>A
n.251T>A
c.1886T>A (p.Ile629Asn)
7g.107701987T>CCA368843713SLC26A4c.1964T>C (p.Ile655Thr)
c.675T>C
n.251T>C
c.1886T>C (p.Ile629Thr)
7g.107701987T>GCA368843715SLC26A4c.1964T>G (p.Ile655Ser)
c.675T>G
n.251T>G
c.1886T>G (p.Ile629Ser)
7g.107701987_107701988delinsTCCA1732759388SLC26A4c.1964_1965delinsTC (p.Ile655=)
c.675_676delinsTC
n.251_252delinsTC
c.1886_1887delinsTC (p.Ile629=)
7g.107701988C>ACA457103439SLC26A4c.1965C>A (p.Ile655=)
c.676C>A
n.252C>A
c.1887C>A (p.Ile629=)
 dbSNP gnomAD v2 gnomAD v4
7g.107701988C=CA1732759402SLC26A4c.1965C= (p.Ile655=)
c.676C=
n.252C=
c.1887C= (p.Ile629=)
7g.107701988C>GCA368843716SLC26A4c.1965C>G (p.Ile655Met)
c.676C>G
n.252C>G
c.1887C>G (p.Ile629Met)
7g.107701988C>TCA4432991SLC26A4c.1965C>T (p.Ile655=)
c.676C>T
n.252C>T
c.1887C>T (p.Ile629=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107701989delCA16041116SLC26A4c.1966del (p.His656IlefsTer18)
c.677del
n.253del
c.1888del (p.His630IlefsTer18)
 ClinVar dbSNP
7g.107701989C>ACA368843722SLC26A4c.1966C>A (p.His656Asn)
c.677C>A
n.253C>A
c.1888C>A (p.His630Asn)
7g.107701989C=CA1732759411SLC26A4c.1966C= (p.His656=)
c.677C=
n.253C=
c.1888C= (p.His630=)
7g.107701989C>GCA164218597SLC26A4c.1966C>G (p.His656Asp)
c.677C>G
n.253C>G
c.1888C>G (p.His630Asp)
 dbSNP
7g.107701989C>TCA368843721SLC26A4c.1966C>T (p.His656Tyr)
c.677C>T
n.253C>T
c.1888C>T (p.His630Tyr)
 dbSNP
7g.107701990A>CCA368843724SLC26A4c.1967A>C (p.His656Pro)
c.678A>C
n.254A>C
c.1889A>C (p.His630Pro)
7g.107701990A>GCA368843725SLC26A4c.1967A>G (p.His656Arg)
c.678A>G
n.254A>G
c.1889A>G (p.His630Arg)
7g.107701990A>TCA368843727SLC26A4c.1967A>T (p.His656Leu)
c.678A>T
n.254A>T
c.1889A>T (p.His630Leu)
7g.107701991T>ACA368843729SLC26A4c.1968T>A (p.His656Gln)
c.679T>A
n.255T>A
c.1890T>A (p.His630Gln)
7g.107701991T>CCA457103460SLC26A4c.1968T>C (p.His656=)
c.679T>C
n.255T>C
c.1890T>C (p.His630=)
 gnomAD v4
7g.107701991T>GCA368843733SLC26A4c.1968T>G (p.His656Gln)
c.679T>G
n.255T>G
c.1890T>G (p.His630Gln)
7g.107701992A=CA1732759417SLC26A4c.1969A= (p.Ser657=)
c.680A=
n.256A=
c.1891A= (p.Ser631=)
7g.107701992A>CCA368843735SLC26A4c.1969A>C (p.Ser657Arg)
c.680A>C
n.256A>C
c.1891A>C (p.Ser631Arg)
7g.107701992A>GCA368843737SLC26A4c.1969A>G (p.Ser657Gly)
c.680A>G
n.256A>G
c.1891A>G (p.Ser631Gly)
7g.107701992A>TCA10576714SLC26A4c.1969A>T (p.Ser657Cys)
c.680A>T
n.256A>T
c.1891A>T (p.Ser631Cys)
 ClinVar dbSNP gnomAD v4
7g.107701993G>ACA368843741SLC26A4c.1970G>A (p.Ser657Asn)
c.681G>A
n.257G>A
c.1892G>A (p.Ser631Asn)
 ClinVar dbSNP
7g.107701993G>CCA368843740SLC26A4c.1970G>C (p.Ser657Thr)
c.681G>C
n.257G>C
c.1892G>C (p.Ser631Thr)
7g.107701993G=CA1732759424SLC26A4c.1970G= (p.Ser657=)
c.681G=
n.257G=
c.1892G= (p.Ser631=)
7g.107701993G>TCA368843739SLC26A4c.1970G>T (p.Ser657Ile)
c.681G>T
n.257G>T
c.1892G>T (p.Ser631Ile)
7g.107701994C>ACA368843742SLC26A4c.1971C>A (p.Ser657Arg)
c.682C>A
n.258C>A
c.1893C>A (p.Ser631Arg)
 ClinVar dbSNP
7g.107701994C=CA1732759432SLC26A4c.1971C= (p.Ser657=)
c.682C=
n.258C=
c.1893C= (p.Ser631=)
7g.107701994C>GCA368843743SLC26A4c.1971C>G (p.Ser657Arg)
c.682C>G
n.258C>G
c.1893C>G (p.Ser631Arg)
7g.107701994C>TCA457103480SLC26A4c.1971C>T (p.Ser657=)
c.682C>T
n.258C>T
c.1893C>T (p.Ser631=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107701994_107702000delinsCCTTGTGCA1732759430SLC26A4c.1971_1977delinsCCTTGTG (p.Ser657=)
c.682_688delinsCCTTGTG
n.258_264delinsCCTTGTG
c.1893_1899delinsCCTTGTG (p.Ser631=)
7g.107701995C>ACA368843744SLC26A4c.1972C>A (p.Leu658Ile)
c.683C>A
n.259C>A
c.1894C>A (p.Leu632Ile)
 dbSNP COSMIC
7g.107701995C=CA1732759436SLC26A4c.1972C= (p.Leu658=)
c.683C=
n.259C=
c.1894C= (p.Leu632=)
7g.107701995C>GCA368843745SLC26A4c.1972C>G (p.Leu658Val)
c.683C>G
n.259C>G
c.1894C>G (p.Leu632Val)
7g.107701995C>TCA368843746SLC26A4c.1972C>T (p.Leu658Phe)
c.683C>T
n.259C>T
c.1894C>T (p.Leu632Phe)
 dbSNP gnomAD v2 gnomAD v4
7g.107701999_107702004delCA1105621052SLC26A4c.1976_1981del (p.Val659_Leu660del)
c.687_692del
n.263_268del
c.1898_1903del (p.Val633_Leu634del)
 dbSNP gnomAD v3 gnomAD v4
7g.107701996T>ACA368843747SLC26A4c.1973T>A (p.Leu658His)
c.684T>A
n.260T>A
c.1895T>A (p.Leu632His)
7g.107701996T>CCA368843748SLC26A4c.1973T>C (p.Leu658Pro)
c.684T>C
n.260T>C
c.1895T>C (p.Leu632Pro)
 dbSNP
7g.107701996T>GCA368843749SLC26A4c.1973T>G (p.Leu658Arg)
c.684T>G
n.260T>G
c.1895T>G (p.Leu632Arg)
7g.107701997T>ACA457103497SLC26A4c.1974T>A (p.Leu658=)
c.685T>A
n.261T>A
c.1896T>A (p.Leu632=)
7g.107701997T>CCA457103499SLC26A4c.1974T>C (p.Leu658=)
c.685T>C
n.261T>C
c.1896T>C (p.Leu632=)
7g.107701997T>GCA457103501SLC26A4c.1974T>G (p.Leu658=)
c.685T>G
n.261T>G
c.1896T>G (p.Leu632=)
7g.107701998G>ACA368843750SLC26A4c.1975G>A (p.Val659Met)
c.686G>A
n.262G>A
c.1897G>A (p.Val633Met)
7g.107701998G>CCA274086SLC26A4c.1975G>C (p.Val659Leu)
c.686G>C
n.262G>C
c.1897G>C (p.Val633Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107701998G=CA1732759446SLC26A4c.1975G= (p.Val659=)
c.686G=
n.262G=
c.1897G= (p.Val633=)
7g.107701998G>TCA368843751SLC26A4c.1975G>T (p.Val659Leu)
c.686G>T
n.262G>T
c.1897G>T (p.Val633Leu)
7g.107701999delCA2777355836SLC26A4c.1976del (p.Val659GlyfsTer15)
c.687del
n.263del
c.1898del (p.Val633GlyfsTer15)
7g.107701999T>ACA368843755SLC26A4c.1976T>A (p.Val659Glu)
c.687T>A
n.263T>A
c.1898T>A (p.Val633Glu)
7g.107701999T>CCA368843754SLC26A4c.1976T>C (p.Val659Ala)
c.687T>C
n.263T>C
c.1898T>C (p.Val633Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.107701999T>GCA368843753SLC26A4c.1976T>G (p.Val659Gly)
c.687T>G
n.263T>G
c.1898T>G (p.Val633Gly)
7g.107701999T=CA1732759452SLC26A4c.1976T= (p.Val659=)
c.687T=
n.263T=
c.1898T= (p.Val633=)
7g.107702000G>ACA457103516SLC26A4c.1977G>A (p.Val659=)
c.688G>A
n.264G>A
c.1899G>A (p.Val633=)
7g.107702000G>CCA457103518SLC26A4c.1977G>C (p.Val659=)
c.688G>C
n.264G>C
c.1899G>C (p.Val633=)
7g.107702000G>TCA457103520SLC26A4c.1977G>T (p.Val659=)
c.688G>T
n.264G>T
c.1899G>T (p.Val633=)
 gnomAD v4
7g.107702001C>ACA368843756SLC26A4c.1978C>A (p.Leu660Ile)
c.689C>A
n.265C>A
c.1900C>A (p.Leu634Ile)
7g.107702001C>GCA368843758SLC26A4c.1978C>G (p.Leu660Val)
c.689C>G
n.265C>G
c.1900C>G (p.Leu634Val)
7g.107702001C>TCA368843757SLC26A4c.1978C>T (p.Leu660Phe)
c.689C>T
n.265C>T
c.1900C>T (p.Leu634Phe)
 gnomAD v4
7g.107702002T>ACA368843759SLC26A4c.1979T>A (p.Leu660His)
c.690T>A
n.266T>A
c.1901T>A (p.Leu634His)
7g.107702002T>CCA368843760SLC26A4c.1979T>C (p.Leu660Pro)
c.690T>C
n.266T>C
c.1901T>C (p.Leu634Pro)
 ClinVar dbSNP
7g.107702002T>GCA368843761SLC26A4c.1979T>G (p.Leu660Arg)
c.690T>G
n.266T>G
c.1901T>G (p.Leu634Arg)
7g.107702003T>ACA457103853SLC26A4c.1980T>A (p.Leu660=)
c.691T>A
n.267T>A
c.1902T>A (p.Leu634=)
7g.107702003T>CCA457103854SLC26A4c.1980T>C (p.Leu660=)
c.691T>C
n.267T>C
c.1902T>C (p.Leu634=)
 ClinVar dbSNP gnomAD v4
7g.107702003T>GCA457103855SLC26A4c.1980T>G (p.Leu660=)
c.691T>G
n.267T>G
c.1902T>G (p.Leu634=)
7g.107702004G>ACA368843762SLC26A4c.1981G>A (p.Asp661Asn)
c.692G>A
n.268G>A
c.1903G>A (p.Asp635Asn)
7g.107702004G>CCA368843763SLC26A4c.1981G>C (p.Asp661His)
c.692G>C
n.268G>C
c.1903G>C (p.Asp635His)
7g.107702004G>TCA368843764SLC26A4c.1981G>T (p.Asp661Tyr)
c.692G>T
n.268G>T
c.1903G>T (p.Asp635Tyr)
7g.107702005A=CA1732759456SLC26A4c.1982A= (p.Asp661=)
c.693A=
n.269A=
c.1904A= (p.Asp635=)
7g.107702005A>CCA368843765SLC26A4c.1982A>C (p.Asp661Ala)
c.693A>C
n.269A>C
c.1904A>C (p.Asp635Ala)
7g.107702005A>GCA368843766SLC26A4c.1982A>G (p.Asp661Gly)
c.693A>G
n.269A>G
c.1904A>G (p.Asp635Gly)
7g.107702005A>TCA368843767SLC26A4c.1982A>T (p.Asp661Val)
c.693A>T
n.269A>T
c.1904A>T (p.Asp635Val)
 dbSNP
7g.107702006C>ACA132687SLC26A4c.1983C>A (p.Asp661Glu)
c.694C>A
n.270C>A
c.1905C>A (p.Asp635Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107702006C=CA1732759462SLC26A4c.1983C= (p.Asp661=)
c.694C=
n.270C=
c.1905C= (p.Asp635=)
7g.107702006C>GCA368843768SLC26A4c.1983C>G (p.Asp661Glu)
c.694C>G
n.270C>G
c.1905C>G (p.Asp635Glu)
7g.107702006C>TCA457103856SLC26A4c.1983C>T (p.Asp661=)
c.694C>T
n.270C>T
c.1905C>T (p.Asp635=)
 gnomAD v4
7g.107702008_107702021delCA2580076173SLC26A4c.1985_1998del (p.Cys662PhefsTer21)
c.696_709del
n.272_285del
c.1907_1920del (p.Cys636PhefsTer21)
 ClinVar
7g.107702007T>ACA368843771SLC26A4c.1984T>A (p.Cys662Ser)
c.695T>A
n.271T>A
c.1906T>A (p.Cys636Ser)
7g.107702007T>CCA368843770SLC26A4c.1984T>C (p.Cys662Arg)
c.695T>C
n.271T>C
c.1906T>C (p.Cys636Arg)
7g.107702007T>GCA368843769SLC26A4c.1984T>G (p.Cys662Gly)
c.695T>G
n.271T>G
c.1906T>G (p.Cys636Gly)
 gnomAD v4
7g.107702007dupCA831169597SLC26A4c.1984dup (p.Cys662LeufsTer26)
c.695dup
n.271dup
c.1906dup (p.Cys636LeufsTer26)
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.107702008G>ACA368843772SLC26A4c.1985G>A (p.Cys662Tyr)
c.696G>A
n.272G>A
c.1907G>A (p.Cys636Tyr)
 ClinVar dbSNP
7g.107702008G>CCA368843773SLC26A4c.1985G>C (p.Cys662Ser)
c.696G>C
n.272G>C
c.1907G>C (p.Cys636Ser)
7g.107702008G>TCA368843774SLC26A4c.1985G>T (p.Cys662Phe)
c.696G>T
n.272G>T
c.1907G>T (p.Cys636Phe)
7g.107702009T>ACA368843775SLC26A4c.1986T>A (p.Cys662Ter)
c.697T>A
n.273T>A
c.1908T>A (p.Cys636Ter)
7g.107702009T>CCA457103857SLC26A4c.1986T>C (p.Cys662=)
c.697T>C
n.273T>C
c.1908T>C (p.Cys636=)
 ClinVar
7g.107702009T>GCA368843776SLC26A4c.1986T>G (p.Cys662Trp)
c.697T>G
n.273T>G
c.1908T>G (p.Cys636Trp)
 gnomAD v4
7g.107702010G>ACA368843777SLC26A4c.1987G>A (p.Gly663Arg)
c.698G>A
n.274G>A
c.1909G>A (p.Gly637Arg)
 ClinVar dbSNP gnomAD v4
7g.107702010G>CCA368843778SLC26A4c.1987G>C (p.Gly663Arg)
c.698G>C
n.274G>C
c.1909G>C (p.Gly637Arg)
7g.107702010G=CA1732759473SLC26A4c.1987G= (p.Gly663=)
c.698G=
n.274G=
c.1909G= (p.Gly637=)
7g.107702010G>TCA368843779SLC26A4c.1987G>T (p.Gly663Ter)
c.698G>T
n.274G>T
c.1909G>T (p.Gly637Ter)
7g.107702011G>ACA368843780SLC26A4c.1988G>A (p.Gly663Glu)
c.699G>A
n.275G>A
c.1910G>A (p.Gly637Glu)
 dbSNP gnomAD v4
7g.107702011G>CCA368843781SLC26A4c.1988G>C (p.Gly663Ala)
c.699G>C
n.275G>C
c.1910G>C (p.Gly637Ala)
7g.107702011G=CA1732759476SLC26A4c.1988G= (p.Gly663=)
c.699G=
n.275G=
c.1910G= (p.Gly637=)
7g.107702011G>TCA368843782SLC26A4c.1988G>T (p.Gly663Val)
c.699G>T
n.275G>T
c.1910G>T (p.Gly637Val)
7g.107702012A>CCA457103860SLC26A4c.1989A>C (p.Gly663=)
c.700A>C
n.276A>C
c.1911A>C (p.Gly637=)
7g.107702012A>GCA457103859SLC26A4c.1989A>G (p.Gly663=)
c.700A>G
n.276A>G
c.1911A>G (p.Gly637=)
7g.107702012A>TCA457103858SLC26A4c.1989A>T (p.Gly663=)
c.700A>T
n.276A>T
c.1911A>T (p.Gly637=)
7g.107702013G>ACA368843785SLC26A4c.1990G>A (p.Ala664Thr)
c.701G>A
n.277G>A
c.1912G>A (p.Ala638Thr)
 dbSNP
7g.107702013G>CCA368843784SLC26A4c.1990G>C (p.Ala664Pro)
c.701G>C
n.277G>C
c.1912G>C (p.Ala638Pro)
7g.107702013G=CA1732759478SLC26A4c.1990G= (p.Ala664=)
c.701G=
n.277G=
c.1912G= (p.Ala638=)
7g.107702013G>TCA368843783SLC26A4c.1990G>T (p.Ala664Ser)
c.701G>T
n.277G>T
c.1912G>T (p.Ala638Ser)
7g.107702014C>ACA368843786SLC26A4c.1991C>A (p.Ala664Asp)
c.702C>A
n.278C>A
c.1913C>A (p.Ala638Asp)
 gnomAD v4
7g.107702014C>GCA368843787SLC26A4c.1991C>G (p.Ala664Gly)
c.702C>G
n.278C>G
c.1913C>G (p.Ala638Gly)
7g.107702014C>TCA368843788SLC26A4c.1991C>T (p.Ala664Val)
c.702C>T
n.278C>T
c.1913C>T (p.Ala638Val)
 ClinVar dbSNP gnomAD v4
7g.107702015T>ACA457103861SLC26A4c.1992T>A (p.Ala664=)
c.703T>A
n.279T>A
c.1914T>A (p.Ala638=)
7g.107702015T>CCA457103862SLC26A4c.1992T>C (p.Ala664=)
c.703T>C
n.279T>C
c.1914T>C (p.Ala638=)
7g.107702015T>GCA457103863SLC26A4c.1992T>G (p.Ala664=)
c.703T>G
n.279T>G
c.1914T>G (p.Ala638=)
7g.107702016A=CA1732759482SLC26A4c.1993A= (p.Ile665=)
c.704A=
n.280A=
c.1915A= (p.Ile639=)
7g.107702016A>CCA368843789SLC26A4c.1993A>C (p.Ile665Leu)
c.704A>C
n.280A>C
c.1915A>C (p.Ile639Leu)
7g.107702016A>GCA4432992SLC26A4c.1993A>G (p.Ile665Val)
c.704A>G
n.280A>G
c.1915A>G (p.Ile639Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107702016A>TCA368843790SLC26A4c.1993A>T (p.Ile665Leu)
c.704A>T
n.280A>T
c.1915A>T (p.Ile639Leu)
7g.107702017T>ACA368843793SLC26A4c.1994T>A (p.Ile665Lys)
c.705T>A
n.281T>A
c.1916T>A (p.Ile639Lys)
7g.107702017T>CCA368843791SLC26A4c.1994T>C (p.Ile665Thr)
c.705T>C
n.281T>C
c.1916T>C (p.Ile639Thr)
 dbSNP
7g.107702017T>GCA368843792SLC26A4c.1994T>G (p.Ile665Arg)
c.705T>G
n.281T>G
c.1916T>G (p.Ile639Arg)
7g.107702017T=CA1732759491SLC26A4c.1994T= (p.Ile665=)
c.705T=
n.281T=
c.1916T= (p.Ile639=)
7g.107702018A=CA1732759497SLC26A4c.1995A= (p.Ile665=)
c.706A=
n.282A=
c.1917A= (p.Ile639=)
7g.107702018A>CCA4432993SLC26A4c.1995A>C (p.Ile665=)
c.706A>C
n.282A>C
c.1917A>C (p.Ile639=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107702018A>GCA368843794SLC26A4c.1995A>G (p.Ile665Met)
c.706A>G
n.282A>G
c.1917A>G (p.Ile639Met)
 dbSNP gnomAD v4
7g.107702018A>TCA457103864SLC26A4c.1995A>T (p.Ile665=)
c.706A>T
n.282A>T
c.1917A>T (p.Ile639=)
7g.107702019T>ACA132689SLC26A4c.1996T>A (p.Ser666Thr)
c.707T>A
n.283T>A
c.1918T>A (p.Ser640Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107702019T>CCA4432994SLC26A4c.1996T>C (p.Ser666Pro)
c.707T>C
n.283T>C
c.1918T>C (p.Ser640Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.107702019T>GCA368843795SLC26A4c.1996T>G (p.Ser666Ala)
c.707T>G
n.283T>G
c.1918T>G (p.Ser640Ala)
7g.107702019T=CA1732759504SLC26A4c.1996T= (p.Ser666=)
c.707T=
n.283T=
c.1918T= (p.Ser640=)
7g.107702020C>ACA368843796SLC26A4c.1997C>A (p.Ser666Tyr)
c.708C>A
n.284C>A
c.1919C>A (p.Ser640Tyr)
 gnomAD v4
7g.107702020C=CA1732759511SLC26A4c.1997C= (p.Ser666=)
c.708C=
n.284C=
c.1919C= (p.Ser640=)
7g.107702020C>GCA368843798SLC26A4c.1997C>G (p.Ser666Cys)
c.708C>G
n.284C>G
c.1919C>G (p.Ser640Cys)
7g.107702020C>TCA368843797SLC26A4c.1997C>T (p.Ser666Phe)
c.708C>T
n.284C>T
c.1919C>T (p.Ser640Phe)
 ClinVar dbSNP
7g.107702021T>ACA457103865SLC26A4c.1998T>A (p.Ser666=)
c.709T>A
n.285T>A
c.1920T>A (p.Ser640=)
 ClinVar
7g.107702021T>CCA4432995SLC26A4c.1998T>C (p.Ser666=)
c.709T>C
n.285T>C
c.1920T>C (p.Ser640=)
 dbSNP ExAC gnomAD v2
7g.107702021T>GCA457103866SLC26A4c.1998T>G (p.Ser666=)
c.709T>G
n.285T>G
c.1920T>G (p.Ser640=)
7g.107702021T=CA1732759515SLC26A4c.1998T= (p.Ser666=)
c.709T=
n.285T=
c.1920T= (p.Ser640=)
7g.107702022T>ACA368843799SLC26A4c.1999T>A (p.Phe667Ile)
c.710T>A
n.286T>A
c.1921T>A (p.Phe641Ile)
7g.107702022T>CCA368843800SLC26A4c.1999T>C (p.Phe667Leu)
c.710T>C
n.286T>C
c.1921T>C (p.Phe641Leu)
 ClinVar
7g.107702022T>GCA368843801SLC26A4c.1999T>G (p.Phe667Val)
c.710T>G
n.286T>G
c.1921T>G (p.Phe641Val)
7g.107702023T>ACA368843802SLC26A4c.2000T>A (p.Phe667Tyr)
c.711T>A
n.287T>A
c.1922T>A (p.Phe641Tyr)
7g.107702023T>CCA368843803SLC26A4c.2000T>C (p.Phe667Ser)
c.711T>C
n.287T>C
c.1922T>C (p.Phe641Ser)
 ClinVar dbSNP gnomAD v4
7g.107702023T>GCA253303SLC26A4c.2000T>G (p.Phe667Cys)
c.711T>G
n.287T>G
c.1922T>G (p.Phe641Cys)
 ClinVar dbSNP
7g.107702023T=CA1732759521SLC26A4c.2000T= (p.Phe667=)
c.711T=
n.287T=
c.1922T= (p.Phe641=)
7g.107702024C>ACA368843804SLC26A4c.2001C>A (p.Phe667Leu)
c.712C>A
n.288C>A
c.1923C>A (p.Phe641Leu)
7g.107702024C>GCA368843805SLC26A4c.2001C>G (p.Phe667Leu)
c.712C>G
n.288C>G
c.1923C>G (p.Phe641Leu)
7g.107702024C>TCA457103867SLC26A4c.2001C>T (p.Phe667=)
c.712C>T
n.288C>T
c.1923C>T (p.Phe641=)
7g.107702025C>ACA368843806SLC26A4c.2002C>A (p.Leu668Met)
c.713C>A
n.289C>A
c.1924C>A (p.Leu642Met)
7g.107702025C>GCA368843807SLC26A4c.2002C>G (p.Leu668Val)
c.713C>G
n.289C>G
c.1924C>G (p.Leu642Val)
7g.107702025C>TCA457103868SLC26A4c.2002C>T (p.Leu668=)
c.713C>T
n.289C>T
c.1924C>T (p.Leu642=)
7g.107702026T>ACA368843809SLC26A4c.2003T>A (p.Leu668Gln)
c.714T>A
n.290T>A
c.1925T>A (p.Leu642Gln)
7g.107702026T>CCA180675SLC26A4c.2003T>C (p.Leu668Pro)
c.714T>C
n.290T>C
c.1925T>C (p.Leu642Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107702026T>GCA368843808SLC26A4c.2003T>G (p.Leu668Arg)
c.714T>G
n.290T>G
c.1925T>G (p.Leu642Arg)
7g.107702026T=CA1732759527SLC26A4c.2003T= (p.Leu668=)
c.714T=
n.290T=
c.1925T= (p.Leu642=)
7g.107702027G>ACA457103869SLC26A4c.2004G>A (p.Leu668=)
c.715G>A
n.291G>A
c.1926G>A (p.Leu642=)
 gnomAD v4
7g.107702027G>CCA457103870SLC26A4c.2004G>C (p.Leu668=)
c.715G>C
n.291G>C
c.1926G>C (p.Leu642=)
7g.107702027G=CA1732759532SLC26A4c.2004G= (p.Leu668=)
c.715G=
n.291G=
c.1926G= (p.Leu642=)
7g.107702027G>TCA457103871SLC26A4c.2004G>T (p.Leu668=)
c.715G>T
n.291G>T
c.1926G>T (p.Leu642=)
7g.107702028G>ACA4432996SLC26A4c.2005G>A (p.Asp669Asn)
c.716G>A
n.292G>A
c.1927G>A (p.Asp643Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107702028G>CCA368843810SLC26A4c.2005G>C (p.Asp669His)
c.716G>C
n.292G>C
c.1927G>C (p.Asp643His)
 dbSNP
7g.107702028G=CA1732759539SLC26A4c.2005G= (p.Asp669=)
c.716G=
n.292G=
c.1927G= (p.Asp643=)
7g.107702028G>TCA368843811SLC26A4c.2005G>T (p.Asp669Tyr)
c.716G>T
n.292G>T
c.1927G>T (p.Asp643Tyr)
7g.107702028_107702029dupCA831169634SLC26A4c.2005_2006dup (p.Asp669GlufsTer6)
c.716_717dup
n.292_293dup
c.1927_1928dup (p.Asp643GlufsTer6)
 ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched