Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.149981484A>CCA361709244SLC26A2c.1891A>C (p.Ile631Leu)
c.372+3133A>C (n.372+3133A>C)
5g.149981484A>GCA361709245SLC26A2c.1891A>G (p.Ile631Val)
c.372+3133A>G (n.372+3133A>G)
5g.149981484A>TCA361709242SLC26A2c.1891A>T (p.Ile631Phe)
c.372+3133A>T (n.372+3133A>T)
5g.149981485T>ACA361709248SLC26A2c.1892T>A (p.Ile631Asn)
c.372+3134T>A (n.372+3134T>A)
5g.149981485T>CCA361709250SLC26A2c.1892T>C (p.Ile631Thr)
c.372+3134T>C (n.372+3134T>C)
5g.149981485T>GCA361709252SLC26A2c.1892T>G (p.Ile631Ser)
c.372+3134T>G (n.372+3134T>G)
5g.149981486C>ACA447402879SLC26A2c.1893C>A (p.Ile631=)
c.372+3135C>A (n.372+3135C>A)
5g.149981486C>GCA361709253SLC26A2c.1893C>G (p.Ile631Met)
c.372+3135C>G (n.372+3135C>G)
5g.149981486C>TCA447402881SLC26A2c.1893C>T (p.Ile631=)
c.372+3135C>T (n.372+3135C>T)
5g.149981487C>ACA361709255SLC26A2c.1894C>A (p.Gln632Lys)
c.372+3136C>A (n.372+3136C>A)
5g.149981487C>GCA361709257SLC26A2c.1894C>G (p.Gln632Glu)
c.372+3136C>G (n.372+3136C>G)
5g.149981487C>TCA361709259SLC26A2c.1894C>T (p.Gln632Ter)
c.372+3136C>T (n.372+3136C>T)
5g.149981488A>CCA361709261SLC26A2c.1895A>C (p.Gln632Pro)
c.372+3137A>C (n.372+3137A>C)
5g.149981488A>GCA361709262SLC26A2c.1895A>G (p.Gln632Arg)
c.372+3137A>G (n.372+3137A>G)
gnomAD v4
5g.149981488A>TCA361709264SLC26A2c.1895A>T (p.Gln632Leu)
c.372+3137A>T (n.372+3137A>T)
5g.149981489G>ACA447402922SLC26A2c.1896G>A (p.Gln632=)
c.372+3138G>A (n.372+3138G>A)
5g.149981489G>CCA361709267SLC26A2c.1896G>C (p.Gln632His)
c.372+3138G>C (n.372+3138G>C)
5g.149981489G>TCA361709268SLC26A2c.1896G>T (p.Gln632His)
c.372+3138G>T (n.372+3138G>T)
5g.149981490G>ACA3505513SLC26A2c.1897G>A (p.Asp633Asn)
c.372+3139G>A (n.372+3139G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149981490G>CCA361709273SLC26A2c.1897G>C (p.Asp633His)
c.372+3139G>C (n.372+3139G>C)
dbSNP gnomAD v3 gnomAD v4
5g.149981490G=CA1590738798SLC26A2c.1897G= (p.Asp633=)
c.372+3139G= (n.372+3139G=)
5g.149981490G>TCA361709271SLC26A2c.1897G>T (p.Asp633Tyr)
c.372+3139G>T (n.372+3139G>T)
5g.149981491A=CA1590738799SLC26A2c.1898A= (p.Asp633=)
c.372+3140A= (n.372+3140A=)
5g.149981491A>CCA361709275SLC26A2c.1898A>C (p.Asp633Ala)
c.372+3140A>C (n.372+3140A>C)
5g.149981491A>GCA361709277SLC26A2c.1898A>G (p.Asp633Gly)
c.372+3140A>G (n.372+3140A>G)
5g.149981491A>TCA361709278SLC26A2c.1898A>T (p.Asp633Val)
c.372+3140A>T (n.372+3140A>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.149981492T>ACA361709279SLC26A2c.1899T>A (p.Asp633Glu)
c.372+3141T>A (n.372+3141T>A)
5g.149981492T>CCA447402923SLC26A2c.1899T>C (p.Asp633=)
c.372+3141T>C (n.372+3141T>C)
5g.149981492T>GCA361709281SLC26A2c.1899T>G (p.Asp633Glu)
c.372+3141T>G (n.372+3141T>G)
5g.149981493G>ACA361709286SLC26A2c.1900G>A (p.Glu634Lys)
c.372+3142G>A (n.372+3142G>A)
dbSNP gnomAD v4
5g.149981493G>CCA361709282SLC26A2c.1900G>C (p.Glu634Gln)
c.372+3142G>C (n.372+3142G>C)
5g.149981493G=CA1590738800SLC26A2c.1900G= (p.Glu634=)
c.372+3142G= (n.372+3142G=)
5g.149981493G>TCA361709284SLC26A2c.1900G>T (p.Glu634Ter)
c.372+3142G>T (n.372+3142G>T)
5g.149981494A>CCA361709288SLC26A2c.1901A>C (p.Glu634Ala)
c.372+3143A>C (n.372+3143A>C)
5g.149981494A>GCA361709289SLC26A2c.1901A>G (p.Glu634Gly)
c.372+3143A>G (n.372+3143A>G)
5g.149981494A>TCA361709291SLC26A2c.1901A>T (p.Glu634Val)
c.372+3143A>T (n.372+3143A>T)
5g.149981495A=CA1590738801SLC26A2c.1902A= (p.Glu634=)
c.372+3144A= (n.372+3144A=)
5g.149981495A>CCA361709293SLC26A2c.1902A>C (p.Glu634Asp)
c.372+3144A>C (n.372+3144A>C)
5g.149981495A>GCA447402924SLC26A2c.1902A>G (p.Glu634=)
c.372+3144A>G (n.372+3144A>G)
dbSNP
5g.149981495A>TCA361709294SLC26A2c.1902A>T (p.Glu634Asp)
c.372+3144A>T (n.372+3144A>T)
5g.149981495_149981496insGGTTCTTGTCA917607705SLC26A2c.1902_1903insGGTTCTTGT (p.Glu634_Met635insGlySerCys)
c.372+3144_372+3145insGGTTCTTGT (n.372+3144_372+3145insGGTTCTTGT)
dbSNP
5g.149981496A>CCA361709301SLC26A2c.1903A>C (p.Met635Leu)
c.372+3145A>C (n.372+3145A>C)
5g.149981496A>GCA361709299SLC26A2c.1903A>G (p.Met635Val)
c.372+3145A>G (n.372+3145A>G)
gnomAD v4
5g.149981496A>TCA361709297SLC26A2c.1903A>T (p.Met635Leu)
c.372+3145A>T (n.372+3145A>T)
5g.149981497T>ACA361709303SLC26A2c.1904T>A (p.Met635Lys)
c.372+3146T>A (n.372+3146T>A)
5g.149981497T>CCA361709307SLC26A2c.1904T>C (p.Met635Thr)
c.372+3146T>C (n.372+3146T>C)
5g.149981497T>GCA361709305SLC26A2c.1904T>G (p.Met635Arg)
c.372+3146T>G (n.372+3146T>G)
5g.149981498G>ACA129084710SLC26A2c.1905G>A (p.Met635Ile)
c.372+3147G>A (n.372+3147G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.149981498G>CCA361709312SLC26A2c.1905G>C (p.Met635Ile)
c.372+3147G>C (n.372+3147G>C)
dbSNP
5g.149981498G=CA1590738802SLC26A2c.1905G= (p.Met635=)
c.372+3147G= (n.372+3147G=)
5g.149981498G>TCA361709310SLC26A2c.1905G>T (p.Met635Ile)
c.372+3147G>T (n.372+3147G>T)
5g.149981499T>ACA361709315SLC26A2c.1906T>A (p.Ser636Thr)
c.372+3148T>A (n.372+3148T>A)
5g.149981499T>CCA361709318SLC26A2c.1906T>C (p.Ser636Pro)
c.372+3148T>C (n.372+3148T>C)
5g.149981499T>GCA361709317SLC26A2c.1906T>G (p.Ser636Ala)
c.372+3148T>G (n.372+3148T>G)
5g.149981500C>ACA361709321SLC26A2c.1907C>A (p.Ser636Ter)
c.372+3149C>A (n.372+3149C>A)
gnomAD v4
5g.149981500C=CA1590738803SLC26A2c.1907C= (p.Ser636=)
c.372+3149C= (n.372+3149C=)
5g.149981500C>GCA361709322SLC26A2c.1907C>G (p.Ser636Ter)
c.372+3149C>G (n.372+3149C>G)
5g.149981500C>TCA129084715SLC26A2c.1907C>T (p.Ser636Leu)
c.372+3149C>T (n.372+3149C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.149981501A=CA1590738804SLC26A2c.1908A= (p.Ser636=)
c.372+3150A= (n.372+3150A=)
5g.149981501A>CCA447402925SLC26A2c.1908A>C (p.Ser636=)
c.372+3150A>C (n.372+3150A>C)
5g.149981501A>GCA3505514SLC26A2c.1908A>G (p.Ser636=)
c.372+3150A>G (n.372+3150A>G)
ClinVar dbSNP ExAC gnomAD v2
5g.149981501A>TCA447402926SLC26A2c.1908A>T (p.Ser636=)
c.372+3150A>T (n.372+3150A>T)
5g.149981502G>ACA3505515SLC26A2c.1909G>A (p.Val637Met)
c.372+3151G>A (n.372+3151G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.149981502G>CCA361709328SLC26A2c.1909G>C (p.Val637Leu)
c.372+3151G>C (n.372+3151G>C)
5g.149981502G=CA1590738805SLC26A2c.1909G= (p.Val637=)
c.372+3151G= (n.372+3151G=)
5g.149981502G>TCA361709330SLC26A2c.1909G>T (p.Val637Leu)
c.372+3151G>T (n.372+3151G>T)
5g.149981503T>ACA361709333SLC26A2c.1910T>A (p.Val637Glu)
c.372+3152T>A (n.372+3152T>A)
gnomAD v4
5g.149981503T>CCA361709334SLC26A2c.1910T>C (p.Val637Ala)
c.372+3152T>C (n.372+3152T>C)
gnomAD v4
5g.149981503T>GCA361709336SLC26A2c.1910T>G (p.Val637Gly)
c.372+3152T>G (n.372+3152T>G)
5g.149981504G>ACA447402929SLC26A2c.1911G>A (p.Val637=)
c.372+3153G>A (n.372+3153G>A)
dbSNP
5g.149981504G>CCA447402927SLC26A2c.1911G>C (p.Val637=)
c.372+3153G>C (n.372+3153G>C)
5g.149981504G=CA1590738806SLC26A2c.1911G= (p.Val637=)
c.372+3153G= (n.372+3153G=)
5g.149981504G>TCA447402928SLC26A2c.1911G>T (p.Val637=)
c.372+3153G>T (n.372+3153G>T)
gnomAD v4
5g.149981505C>ACA361709342SLC26A2c.1912C>A (p.Gln638Lys)
c.372+3154C>A (n.372+3154C>A)
5g.149981505C=CA1590738807SLC26A2c.1912C= (p.Gln638=)
c.372+3154C= (n.372+3154C=)
5g.149981505C>GCA361709340SLC26A2c.1912C>G (p.Gln638Glu)
c.372+3154C>G (n.372+3154C>G)
5g.149981505C>TCA361709339SLC26A2c.1912C>T (p.Gln638Ter)
c.372+3154C>T (n.372+3154C>T)
dbSNP
5g.149981506A>CCA361709344SLC26A2c.1913A>C (p.Gln638Pro)
c.372+3155A>C (n.372+3155A>C)
5g.149981506A>GCA361709346SLC26A2c.1913A>G (p.Gln638Arg)
c.372+3155A>G (n.372+3155A>G)
5g.149981506A>TCA361709348SLC26A2c.1913A>T (p.Gln638Leu)
c.372+3155A>T (n.372+3155A>T)
5g.149981507A>CCA361709350SLC26A2c.1914A>C (p.Gln638His)
c.372+3156A>C (n.372+3156A>C)
5g.149981507A>GCA447402930SLC26A2c.1914A>G (p.Gln638=)
c.372+3156A>G (n.372+3156A>G)
gnomAD v4
5g.149981507A>TCA361709352SLC26A2c.1914A>T (p.Gln638His)
c.372+3156A>T (n.372+3156A>T)
5g.149981508C>ACA361709354SLC26A2c.1915C>A (p.Leu639Ile)
c.372+3157C>A (n.372+3157C>A)
gnomAD v4
5g.149981508C>GCA361709356SLC26A2c.1915C>G (p.Leu639Val)
c.372+3157C>G (n.372+3157C>G)
5g.149981508C>TCA361709358SLC26A2c.1915C>T (p.Leu639Phe)
c.372+3157C>T (n.372+3157C>T)
5g.149981509T>ACA361709359SLC26A2c.1916T>A (p.Leu639His)
c.372+3158T>A (n.372+3158T>A)
5g.149981509T>CCA361709361SLC26A2c.1916T>C (p.Leu639Pro)
c.372+3158T>C (n.372+3158T>C)
5g.149981509T>GCA361709363SLC26A2c.1916T>G (p.Leu639Arg)
c.372+3158T>G (n.372+3158T>G)
5g.149981510T>ACA447402933SLC26A2c.1917T>A (p.Leu639=)
c.372+3159T>A (n.372+3159T>A)
5g.149981510T>CCA447402931SLC26A2c.1917T>C (p.Leu639=)
c.372+3159T>C (n.372+3159T>C)
5g.149981510T>GCA447402932SLC26A2c.1917T>G (p.Leu639=)
c.372+3159T>G (n.372+3159T>G)
5g.149981511T>ACA361709367SLC26A2c.1918T>A (p.Ser640Thr)
c.372+3160T>A (n.372+3160T>A)
5g.149981511T>CCA361709369SLC26A2c.1918T>C (p.Ser640Pro)
c.372+3160T>C (n.372+3160T>C)
5g.149981511T>GCA361709365SLC26A2c.1918T>G (p.Ser640Ala)
c.372+3160T>G (n.372+3160T>G)
5g.149981512C>ACA361709372SLC26A2c.1919C>A (p.Ser640Tyr)
c.372+3161C>A (n.372+3161C>A)
5g.149981512C>GCA361709374SLC26A2c.1919C>G (p.Ser640Cys)
c.372+3161C>G (n.372+3161C>G)
5g.149981512C>TCA361709376SLC26A2c.1919C>T (p.Ser640Phe)
c.372+3161C>T (n.372+3161C>T)
COSMIC
5g.149981513C>ACA447402934SLC26A2c.1920C>A (p.Ser640=)
c.372+3162C>A (n.372+3162C>A)
5g.149981513C>GCA447402935SLC26A2c.1920C>G (p.Ser640=)
c.372+3162C>G (n.372+3162C>G)
5g.149981513C>TCA447402936SLC26A2c.1920C>T (p.Ser640=)
c.372+3162C>T (n.372+3162C>T)
5g.149981514C>ACA361709378SLC26A2c.1921C>A (p.His641Asn)
c.372+3163C>A (n.372+3163C>A)
5g.149981514C>GCA361709379SLC26A2c.1921C>G (p.His641Asp)
c.372+3163C>G (n.372+3163C>G)
5g.149981514C>TCA361709381SLC26A2c.1921C>T (p.His641Tyr)
c.372+3163C>T (n.372+3163C>T)
gnomAD v4
5g.149981515A=CA1590738808SLC26A2c.1922A= (p.His641=)
c.372+3164A= (n.372+3164A=)
5g.149981515A>CCA361709383SLC26A2c.1922A>C (p.His641Pro)
c.372+3164A>C (n.372+3164A>C)
5g.149981515A>GCA361709384SLC26A2c.1922A>G (p.His641Arg)
c.372+3164A>G (n.372+3164A>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
5g.149981515A>TCA361709385SLC26A2c.1922A>T (p.His641Leu)
c.372+3164A>T (n.372+3164A>T)
5g.149981516T>ACA361709387SLC26A2c.1923T>A (p.His641Gln)
c.372+3165T>A (n.372+3165T>A)
5g.149981516T>CCA447402937SLC26A2c.1923T>C (p.His641=)
c.372+3165T>C (n.372+3165T>C)
5g.149981516T>GCA361709388SLC26A2c.1923T>G (p.His641Gln)
c.372+3165T>G (n.372+3165T>G)
5g.149981517G>ACA361709392SLC26A2c.1924G>A (p.Asp642Asn)
c.372+3166G>A (n.372+3166G>A)
5g.149981517G>CCA361709394SLC26A2c.1924G>C (p.Asp642His)
c.372+3166G>C (n.372+3166G>C)
5g.149981517G>TCA361709390SLC26A2c.1924G>T (p.Asp642Tyr)
c.372+3166G>T (n.372+3166G>T)
5g.149981518A>CCA361709396SLC26A2c.1925A>C (p.Asp642Ala)
c.372+3167A>C (n.372+3167A>C)
5g.149981518A>GCA361709398SLC26A2c.1925A>G (p.Asp642Gly)
c.372+3167A>G (n.372+3167A>G)
5g.149981518A>TCA361709400SLC26A2c.1925A>T (p.Asp642Val)
c.372+3167A>T (n.372+3167A>T)
gnomAD v4
5g.149981518_149981519delCA913108432SLC26A2c.1925_1926del (p.Asp642AlafsTer10)
c.372+3167_372+3168del (n.372+3167_372+3168del)
5g.149981518_149981519delinsATCA1590738809SLC26A2c.1925_1926delinsAT (p.Asp642=)
c.372+3167_372+3168delinsAT (n.372+3167_372+3168delinsAT)
5g.149981519delCA563955709SLC26A2c.1926del (p.Leu644TrpfsTer6)
c.372+3168del (n.372+3168del)
ClinVar dbSNP gnomAD v2 gnomAD v4
5g.149981519T>ACA361709402SLC26A2c.1926T>A (p.Asp642Glu)
c.372+3168T>A (n.372+3168T>A)
dbSNP
5g.149981519T>CCA447402938SLC26A2c.1926T>C (p.Asp642=)
c.372+3168T>C (n.372+3168T>C)
5g.149981519T>GCA361709404SLC26A2c.1926T>G (p.Asp642Glu)
c.372+3168T>G (n.372+3168T>G)
5g.149981520C>ACA361709410SLC26A2c.1927C>A (p.Pro643Thr)
c.372+3169C>A (n.372+3169C>A)
5g.149981520C=CA1590738810SLC26A2c.1927C= (p.Pro643=)
c.372+3169C= (n.372+3169C=)
5g.149981520C>GCA361709407SLC26A2c.1927C>G (p.Pro643Ala)
c.372+3169C>G (n.372+3169C>G)
5g.149981520C>TCA129084726SLC26A2c.1927C>T (p.Pro643Ser)
c.372+3169C>T (n.372+3169C>T)
dbSNP gnomAD v3 gnomAD v4
5g.149981521C>ACA361709412SLC26A2c.1928C>A (p.Pro643His)
c.372+3170C>A (n.372+3170C>A)
5g.149981521C>GCA361709414SLC26A2c.1928C>G (p.Pro643Arg)
c.372+3170C>G (n.372+3170C>G)
gnomAD v4
5g.149981521C>TCA361709416SLC26A2c.1928C>T (p.Pro643Leu)
c.372+3170C>T (n.372+3170C>T)
5g.149981522C>ACA447402939SLC26A2c.1929C>A (p.Pro643=)
c.372+3171C>A (n.372+3171C>A)
5g.149981522C>GCA447402940SLC26A2c.1929C>G (p.Pro643=)
c.372+3171C>G (n.372+3171C>G)
5g.149981522C>TCA447402941SLC26A2c.1929C>T (p.Pro643=)
c.372+3171C>T (n.372+3171C>T)
5g.149981523T>ACA361709417SLC26A2c.1930T>A (p.Leu644Met)
c.372+3172T>A (n.372+3172T>A)
5g.149981523T>CCA447402942SLC26A2c.1930T>C (p.Leu644=)
c.372+3172T>C (n.372+3172T>C)
5g.149981523T>GCA361709419SLC26A2c.1930T>G (p.Leu644Val)
c.372+3172T>G (n.372+3172T>G)
5g.149981524T>ACA361709424SLC26A2c.1931T>A (p.Leu644Ter)
c.372+3173T>A (n.372+3173T>A)
5g.149981524T>CCA361709422SLC26A2c.1931T>C (p.Leu644Ser)
c.372+3173T>C (n.372+3173T>C)
5g.149981524T>GCA361709420SLC26A2c.1931T>G (p.Leu644Trp)
c.372+3173T>G (n.372+3173T>G)
5g.149981525G>ACA447402943SLC26A2c.1932G>A (p.Leu644=)
c.372+3174G>A (n.372+3174G>A)
dbSNP
5g.149981525G>CCA361709426SLC26A2c.1932G>C (p.Leu644Phe)
c.372+3174G>C (n.372+3174G>C)
5g.149981525G>TCA361709428SLC26A2c.1932G>T (p.Leu644Phe)
c.372+3174G>T (n.372+3174G>T)
5g.149981526G>ACA361709430SLC26A2c.1933G>A (p.Glu645Lys)
c.372+3175G>A (n.372+3175G>A)
5g.149981526G>CCA361709432SLC26A2c.1933G>C (p.Glu645Gln)
c.372+3175G>C (n.372+3175G>C)
5g.149981526G>TCA361709434SLC26A2c.1933G>T (p.Glu645Ter)
c.372+3175G>T (n.372+3175G>T)
gnomAD v4
5g.149981527A>CCA361709436SLC26A2c.1934A>C (p.Glu645Ala)
c.372+3176A>C (n.372+3176A>C)
5g.149981527A>GCA361709438SLC26A2c.1934A>G (p.Glu645Gly)
c.372+3176A>G (n.372+3176A>G)
5g.149981527A>TCA361709440SLC26A2c.1934A>T (p.Glu645Val)
c.372+3176A>T (n.372+3176A>T)
5g.149981528G>ACA447402944SLC26A2c.1935G>A (p.Glu645=)
c.372+3177G>A (n.372+3177G>A)
5g.149981528G>CCA361709442SLC26A2c.1935G>C (p.Glu645Asp)
c.372+3177G>C (n.372+3177G>C)
gnomAD v4
5g.149981528G>TCA361709444SLC26A2c.1935G>T (p.Glu645Asp)
c.372+3177G>T (n.372+3177G>T)
5g.149981529C>ACA361709446SLC26A2c.1936C>A (p.Leu646Met)
c.372+3178C>A (n.372+3178C>A)
5g.149981529C>GCA361709448SLC26A2c.1936C>G (p.Leu646Val)
c.372+3178C>G (n.372+3178C>G)
5g.149981529C>TCA447402945SLC26A2c.1936C>T (p.Leu646=)
c.372+3178C>T (n.372+3178C>T)
ClinVar
5g.149981530T>ACA361709454SLC26A2c.1937T>A (p.Leu646Gln)
c.372+3179T>A (n.372+3179T>A)
5g.149981530T>CCA361709452SLC26A2c.1937T>C (p.Leu646Pro)
c.372+3179T>C (n.372+3179T>C)
5g.149981530T>GCA361709450SLC26A2c.1937T>G (p.Leu646Arg)
c.372+3179T>G (n.372+3179T>G)
5g.149981531G>ACA3505516SLC26A2c.1938G>A (p.Leu646=)
c.372+3180G>A (n.372+3180G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149981531G>CCA447402947SLC26A2c.1938G>C (p.Leu646=)
c.372+3180G>C (n.372+3180G>C)
5g.149981531G=CA1590738811SLC26A2c.1938G= (p.Leu646=)
c.372+3180G= (n.372+3180G=)
5g.149981531G>TCA447402946SLC26A2c.1938G>T (p.Leu646=)
c.372+3180G>T (n.372+3180G>T)
5g.149981532C>ACA361709458SLC26A2c.1939C>A (p.His647Asn)
c.372+3181C>A (n.372+3181C>A)
5g.149981532C=CA1590738812SLC26A2c.1939C= (p.His647=)
c.372+3181C= (n.372+3181C=)
5g.149981532C>GCA361709459SLC26A2c.1939C>G (p.His647Asp)
c.372+3181C>G (n.372+3181C>G)
5g.149981532C>TCA361709462SLC26A2c.1939C>T (p.His647Tyr)
c.372+3181C>T (n.372+3181C>T)
ClinVar dbSNP
5g.149981533A>CCA361709464SLC26A2c.1940A>C (p.His647Pro)
c.372+3182A>C (n.372+3182A>C)
5g.149981533A>GCA361709466SLC26A2c.1940A>G (p.His647Arg)
c.372+3182A>G (n.372+3182A>G)
5g.149981533A>TCA361709468SLC26A2c.1940A>T (p.His647Leu)
c.372+3182A>T (n.372+3182A>T)
gnomAD v4
5g.149981534T>ACA361709470SLC26A2c.1941T>A (p.His647Gln)
c.372+3183T>A (n.372+3183T>A)
5g.149981534T>CCA447402948SLC26A2c.1941T>C (p.His647=)
c.372+3183T>C (n.372+3183T>C)
dbSNP
5g.149981534T>GCA361709471SLC26A2c.1941T>G (p.His647Gln)
c.372+3183T>G (n.372+3183T>G)
5g.149981534T=CA1590738813SLC26A2c.1941T= (p.His647=)
c.372+3183T= (n.372+3183T=)
5g.149981535A=CA1590738814SLC26A2c.1942A= (p.Thr648=)
c.372+3184A= (n.372+3184A=)
5g.149981535A>CCA361709475SLC26A2c.1942A>C (p.Thr648Pro)
c.372+3184A>C (n.372+3184A>C)
5g.149981535A>GCA361709476SLC26A2c.1942A>G (p.Thr648Ala)
c.372+3184A>G (n.372+3184A>G)
5g.149981535A>TCA361709477SLC26A2c.1942A>T (p.Thr648Ser)
c.372+3184A>T (n.372+3184A>T)
dbSNP
5g.149981536C>ACA361709479SLC26A2c.1943C>A (p.Thr648Asn)
c.372+3185C>A (n.372+3185C>A)
5g.149981536C=CA1590738815SLC26A2c.1943C= (p.Thr648=)
c.372+3185C= (n.372+3185C=)
5g.149981536C>GCA361709480SLC26A2c.1943C>G (p.Thr648Ser)
c.372+3185C>G (n.372+3185C>G)
5g.149981536C>TCA361709478SLC26A2c.1943C>T (p.Thr648Ile)
c.372+3185C>T (n.372+3185C>T)
dbSNP gnomAD v2 gnomAD v4
5g.149981537T>ACA447402949SLC26A2c.1944T>A (p.Thr648=)
c.372+3186T>A (n.372+3186T>A)
5g.149981537T>CCA3505517SLC26A2c.1944T>C (p.Thr648=)
c.372+3186T>C (n.372+3186T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149981537T>GCA447402950SLC26A2c.1944T>G (p.Thr648=)
c.372+3186T>G (n.372+3186T>G)
COSMIC
5g.149981537T=CA1590738816SLC26A2c.1944T= (p.Thr648=)
c.372+3186T= (n.372+3186T=)
5g.149981539_149981540delCA2675943657SLC26A2c.1946_1947del (p.Ile649SerfsTer3)
c.372+3188_372+3189del (n.372+3188_372+3189del)
gnomAD v4
5g.149981538A=CA1590738817SLC26A2c.1945A= (p.Ile649=)
c.372+3187A= (n.372+3187A=)
5g.149981538A>CCA361709481SLC26A2c.1945A>C (p.Ile649Leu)
c.372+3187A>C (n.372+3187A>C)
5g.149981538A>GCA3505518SLC26A2c.1945A>G (p.Ile649Val)
c.372+3187A>G (n.372+3187A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149981538A>TCA361709482SLC26A2c.1945A>T (p.Ile649Leu)
c.372+3187A>T (n.372+3187A>T)
5g.149981539T>ACA361709483SLC26A2c.1946T>A (p.Ile649Lys)
c.372+3188T>A (n.372+3188T>A)
5g.149981539T>CCA361709484SLC26A2c.1946T>C (p.Ile649Thr)
c.372+3188T>C (n.372+3188T>C)
gnomAD v4
5g.149981539T>GCA361709485SLC26A2c.1946T>G (p.Ile649Arg)
c.372+3188T>G (n.372+3188T>G)
5g.149981540A=CA1590738818SLC26A2c.1947A= (p.Ile649=)
c.372+3189A= (n.372+3189A=)
5g.149981540A>CCA447402951SLC26A2c.1947A>C (p.Ile649=)
c.372+3189A>C (n.372+3189A>C)
ClinVar gnomAD v4
5g.149981540A>GCA3505519SLC26A2c.1947A>G (p.Ile649Met)
c.372+3189A>G (n.372+3189A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.149981540A>TCA447402952SLC26A2c.1947A>T (p.Ile649=)
c.372+3189A>T (n.372+3189A>T)
5g.149981541G>ACA361709486SLC26A2c.1948G>A (p.Val650Met)
c.372+3190G>A (n.372+3190G>A)
5g.149981541G>CCA361709487SLC26A2c.1948G>C (p.Val650Leu)
c.372+3190G>C (n.372+3190G>C)
5g.149981541G>TCA361709488SLC26A2c.1948G>T (p.Val650Leu)
c.372+3190G>T (n.372+3190G>T)
5g.149981542T>ACA361709489SLC26A2c.1949T>A (p.Val650Glu)
c.372+3191T>A (n.372+3191T>A)
5g.149981542T>CCA361709490SLC26A2c.1949T>C (p.Val650Ala)
c.372+3191T>C (n.372+3191T>C)
5g.149981542T>GCA361709491SLC26A2c.1949T>G (p.Val650Gly)
c.372+3191T>G (n.372+3191T>G)
5g.149981542_149981543delinsTGCA1590738819SLC26A2c.1949_1950delinsTG (p.Val650=)
c.372+3191_372+3192delinsTG (n.372+3191_372+3192delinsTG)
5g.149981543delCA3505520SLC26A2c.1950del (p.Ile651LeufsTer9)
c.372+3192del (n.372+3192del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149981543G>ACA447402953SLC26A2c.1950G>A (p.Val650=)
c.372+3192G>A (n.372+3192G>A)
ClinVar gnomAD v4
5g.149981543G>CCA447402954SLC26A2c.1950G>C (p.Val650=)
c.372+3192G>C (n.372+3192G>C)
5g.149981543G>TCA447402955SLC26A2c.1950G>T (p.Val650=)
c.372+3192G>T (n.372+3192G>T)
gnomAD v4
5g.149981544A>CCA361709492SLC26A2c.1951A>C (p.Ile651Leu)
c.372+3193A>C (n.372+3193A>C)
5g.149981544A>GCA361709493SLC26A2c.1951A>G (p.Ile651Val)
c.372+3193A>G (n.372+3193A>G)
5g.149981544A>TCA361709494SLC26A2c.1951A>T (p.Ile651Phe)
c.372+3193A>T (n.372+3193A>T)
5g.149981545T>ACA361709495SLC26A2c.1952T>A (p.Ile651Asn)
c.372+3194T>A (n.372+3194T>A)
5g.149981545T>CCA3505521SLC26A2c.1952T>C (p.Ile651Thr)
c.372+3194T>C (n.372+3194T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
5g.149981545T>GCA361709496SLC26A2c.1952T>G (p.Ile651Ser)
c.372+3194T>G (n.372+3194T>G)
5g.149981545T=CA1590738820SLC26A2c.1952T= (p.Ile651=)
c.372+3194T= (n.372+3194T=)
5g.149981545_149981549delinsTTGACCA1590738821SLC26A2c.1952_1956delinsTTGAC (p.Ile651=)
c.372+3194_372+3198delinsTTGAC (n.372+3194_372+3198delinsTTGAC)
5g.149981546T>ACA447402956SLC26A2c.1953T>A (p.Ile651=)
c.372+3195T>A (n.372+3195T>A)
5g.149981546T>CCA447402957SLC26A2c.1953T>C (p.Ile651=)
c.372+3195T>C (n.372+3195T>C)
5g.149981546T>GCA361709497SLC26A2c.1953T>G (p.Ile651Met)
c.372+3195T>G (n.372+3195T>G)
5g.149981548_149981551delCA16041000SLC26A2c.1955_1958del (p.Asp652AlafsTer7)
c.372+3197_372+3200del (n.372+3197_372+3200del)
ClinVar dbSNP gnomAD v4
5g.149981547G>ACA361709498SLC26A2c.1954G>A (p.Asp652Asn)
c.372+3196G>A (n.372+3196G>A)
dbSNP
5g.149981547G>CCA361709499SLC26A2c.1954G>C (p.Asp652His)
c.372+3196G>C (n.372+3196G>C)
5g.149981547G=CA1590738822SLC26A2c.1954G= (p.Asp652=)
c.372+3196G= (n.372+3196G=)
5g.149981547G>TCA361709500SLC26A2c.1954G>T (p.Asp652Tyr)
c.372+3196G>T (n.372+3196G>T)
5g.149981548A=CA1590738823SLC26A2c.1955A= (p.Asp652=)
c.372+3197A= (n.372+3197A=)
5g.149981548A>CCA361709501SLC26A2c.1955A>C (p.Asp652Ala)
c.372+3197A>C (n.372+3197A>C)
5g.149981548A>GCA361709502SLC26A2c.1955A>G (p.Asp652Gly)
c.372+3197A>G (n.372+3197A>G)
dbSNP
5g.149981548A>TCA361709503SLC26A2c.1955A>T (p.Asp652Val)
c.372+3197A>T (n.372+3197A>T)
5g.149981548dupCA913108433SLC26A2c.1955dup (p.Asp652GlufsTer24)
c.372+3197dup (n.372+3197dup)
5g.149981549C>ACA361709505SLC26A2c.1956C>A (p.Asp652Glu)
c.372+3198C>A (n.372+3198C>A)
5g.149981549C>GCA361709504SLC26A2c.1956C>G (p.Asp652Glu)
c.372+3198C>G (n.372+3198C>G)
5g.149981549C>TCA447402958SLC26A2c.1956C>T (p.Asp652=)
c.372+3198C>T (n.372+3198C>T)
5g.149981549_149981550dupCA658823316SLC26A2c.1956_1957dup (p.Cys653SerfsTer8)
c.372+3198_372+3199dup (n.372+3198_372+3199dup)
ClinVar dbSNP
5g.149981550T>ACA252996SLC26A2c.1957T>A (p.Cys653Ser)
c.372+3199T>A (n.372+3199T>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149981550T>CCA361709506SLC26A2c.1957T>C (p.Cys653Arg)
c.372+3199T>C (n.372+3199T>C)
gnomAD v4
5g.149981550T>GCA361709507SLC26A2c.1957T>G (p.Cys653Gly)
c.372+3199T>G (n.372+3199T>G)
ClinVar gnomAD v4
5g.149981550T=CA1590738824SLC26A2c.1957T= (p.Cys653=)
c.372+3199T= (n.372+3199T=)
5g.149981551G>ACA361709508SLC26A2c.1958G>A (p.Cys653Tyr)
c.372+3200G>A (n.372+3200G>A)
ClinVar dbSNP
5g.149981551G>CCA361709509SLC26A2c.1958G>C (p.Cys653Ser)
c.372+3200G>C (n.372+3200G>C)
5g.149981551G=CA1590738825SLC26A2c.1958G= (p.Cys653=)
c.372+3200G= (n.372+3200G=)
5g.149981551G>TCA361709510SLC26A2c.1958G>T (p.Cys653Phe)
c.372+3200G>T (n.372+3200G>T)
gnomAD v4
5g.149981552C>ACA361709512SLC26A2c.1959C>A (p.Cys653Ter)
c.372+3201C>A (n.372+3201C>A)
5g.149981552C=CA1590738826SLC26A2c.1959C= (p.Cys653=)
c.372+3201C= (n.372+3201C=)
5g.149981552C>GCA361709511SLC26A2c.1959C>G (p.Cys653Trp)
c.372+3201C>G (n.372+3201C>G)
5g.149981552C>TCA447402959SLC26A2c.1959C>T (p.Cys653=)
c.372+3201C>T (n.372+3201C>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
5g.149981553A=CA1590738827SLC26A2c.1960A= (p.Ser654=)
c.372+3202A= (n.372+3202A=)
5g.149981553A>CCA361709513SLC26A2c.1960A>C (p.Ser654Arg)
c.372+3202A>C (n.372+3202A>C)
5g.149981553A>GCA361709514SLC26A2c.1960A>G (p.Ser654Gly)
c.372+3202A>G (n.372+3202A>G)
dbSNP
5g.149981553A>TCA361709515SLC26A2c.1960A>T (p.Ser654Cys)
c.372+3202A>T (n.372+3202A>T)
5g.149981554G>ACA361709516SLC26A2c.1961G>A (p.Ser654Asn)
c.372+3203G>A (n.372+3203G>A)
5g.149981554G>CCA361709517SLC26A2c.1961G>C (p.Ser654Thr)
c.372+3203G>C (n.372+3203G>C)
5g.149981554G>TCA361709518SLC26A2c.1961G>T (p.Ser654Ile)
c.372+3203G>T (n.372+3203G>T)
5g.149981555T>ACA361709520SLC26A2c.1962T>A (p.Ser654Arg)
c.372+3204T>A (n.372+3204T>A)
5g.149981555T>CCA3505522SLC26A2c.1962T>C (p.Ser654=)
c.372+3204T>C (n.372+3204T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
5g.149981555T>GCA361709519SLC26A2c.1962T>G (p.Ser654Arg)
c.372+3204T>G (n.372+3204T>G)
5g.149981555T=CA1590738828SLC26A2c.1962T= (p.Ser654=)
c.372+3204T= (n.372+3204T=)
5g.149981556G>ACA361709521SLC26A2c.1963G>A (p.Ala655Thr)
c.372+3205G>A (n.372+3205G>A)
gnomAD v4
5g.149981556G>CCA361709522SLC26A2c.1963G>C (p.Ala655Pro)
c.372+3205G>C (n.372+3205G>C)
5g.149981556G>TCA361709523SLC26A2c.1963G>T (p.Ala655Ser)
c.372+3205G>T (n.372+3205G>T)
5g.149981557C>ACA361709524SLC26A2c.1964C>A (p.Ala655Glu)
c.372+3206C>A (n.372+3206C>A)
5g.149981557C>GCA361709525SLC26A2c.1964C>G (p.Ala655Gly)
c.372+3206C>G (n.372+3206C>G)
5g.149981557C>TCA361709526SLC26A2c.1964C>T (p.Ala655Val)
c.372+3206C>T (n.372+3206C>T)
gnomAD v4
5g.149981558A>CCA447402960SLC26A2c.1965A>C (p.Ala655=)
c.372+3207A>C (n.372+3207A>C)
5g.149981558A>GCA447402961SLC26A2c.1965A>G (p.Ala655=)
c.372+3207A>G (n.372+3207A>G)
5g.149981558A>TCA447402962SLC26A2c.1965A>T (p.Ala655=)
c.372+3207A>T (n.372+3207A>T)
5g.149981559A=CA1590738829SLC26A2c.1966A= (p.Ile656=)
c.372+3208A= (n.372+3208A=)
5g.149981559A>CCA361709527SLC26A2c.1966A>C (p.Ile656Leu)
c.372+3208A>C (n.372+3208A>C)
dbSNP gnomAD v4
5g.149981559A>GCA3505523SLC26A2c.1966A>G (p.Ile656Val)
c.372+3208A>G (n.372+3208A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149981559A>TCA361709528SLC26A2c.1966A>T (p.Ile656Phe)
c.372+3208A>T (n.372+3208A>T)
5g.149981560T>ACA361709529SLC26A2c.1967T>A (p.Ile656Asn)
c.372+3209T>A (n.372+3209T>A)
5g.149981560T>CCA361709530SLC26A2c.1967T>C (p.Ile656Thr)
c.372+3209T>C (n.372+3209T>C)
5g.149981560T>GCA361709531SLC26A2c.1967T>G (p.Ile656Ser)
c.372+3209T>G (n.372+3209T>G)
5g.149981561delCA2740094150SLC26A2c.1968del (p.Gln657AsnfsTer3)
c.372+3210del (n.372+3210del)
ClinVar
5g.149981561T>ACA447402963SLC26A2c.1968T>A (p.Ile656=)
c.372+3210T>A (n.372+3210T>A)
5g.149981561T>CCA447402964SLC26A2c.1968T>C (p.Ile656=)
c.372+3210T>C (n.372+3210T>C)
5g.149981561T>GCA361709532SLC26A2c.1968T>G (p.Ile656Met)
c.372+3210T>G (n.372+3210T>G)
5g.149981562C>ACA361709535SLC26A2c.1969C>A (p.Gln657Lys)
c.372+3211C>A (n.372+3211C>A)
5g.149981562C>GCA361709533SLC26A2c.1969C>G (p.Gln657Glu)
c.372+3211C>G (n.372+3211C>G)
5g.149981562C>TCA361709534SLC26A2c.1969C>T (p.Gln657Ter)
c.372+3211C>T (n.372+3211C>T)
5g.149981563A>CCA361709536SLC26A2c.1970A>C (p.Gln657Pro)
c.372+3212A>C (n.372+3212A>C)
COSMIC
5g.149981563A>GCA361709537SLC26A2c.1970A>G (p.Gln657Arg)
c.372+3212A>G (n.372+3212A>G)
5g.149981563A>TCA361709538SLC26A2c.1970A>T (p.Gln657Leu)
c.372+3212A>T (n.372+3212A>T)
5g.149981564A=CA1590738831SLC26A2c.1971A= (p.Gln657=)
c.372+3213A= (n.372+3213A=)
5g.149981564A>CCA361709539SLC26A2c.1971A>C (p.Gln657His)
c.372+3213A>C (n.372+3213A>C)
5g.149981564A>GCA129084756SLC26A2c.1971A>G (p.Gln657=)
c.372+3213A>G (n.372+3213A>G)
ClinVar dbSNP gnomAD v3 gnomAD v4
5g.149981564A>TCA361709540SLC26A2c.1971A>T (p.Gln657His)
c.372+3213A>T (n.372+3213A>T)
5g.149981564_149981565delinsATCA1590738830SLC26A2c.1971_1972delinsAT (p.Gln657=)
c.372+3213_372+3214delinsAT (n.372+3213_372+3214delinsAT)
5g.149981565T>ACA361709543SLC26A2c.1972T>A (p.Phe658Ile)
c.372+3214T>A (n.372+3214T>A)
5g.149981565T>CCA361709542SLC26A2c.1972T>C (p.Phe658Leu)
c.372+3214T>C (n.372+3214T>C)
5g.149981565T>GCA361709541SLC26A2c.1972T>G (p.Phe658Val)
c.372+3214T>G (n.372+3214T>G)
5g.149981569delCA263256SLC26A2c.1976del (p.Leu659Ter)
c.372+3218del (n.372+3218del)
ClinVar dbSNP
5g.149981566T>ACA361709544SLC26A2c.1973T>A (p.Phe658Tyr)
c.372+3215T>A (n.372+3215T>A)
5g.149981566T>CCA361709545SLC26A2c.1973T>C (p.Phe658Ser)
c.372+3215T>C (n.372+3215T>C)
5g.149981566T>GCA361709546SLC26A2c.1973T>G (p.Phe658Cys)
c.372+3215T>G (n.372+3215T>G)
5g.149981567T>ACA361709547SLC26A2c.1974T>A (p.Phe658Leu)
c.372+3216T>A (n.372+3216T>A)
5g.149981567T>CCA447402965SLC26A2c.1974T>C (p.Phe658=)
c.372+3216T>C (n.372+3216T>C)
5g.149981567T>GCA361709548SLC26A2c.1974T>G (p.Phe658Leu)
c.372+3216T>G (n.372+3216T>G)
5g.149981568T>ACA361709549SLC26A2c.1975T>A (p.Leu659Ile)
c.372+3217T>A (n.372+3217T>A)
5g.149981568T>CCA447402966SLC26A2c.1975T>C (p.Leu659=)
c.372+3217T>C (n.372+3217T>C)
5g.149981568T>GCA361709550SLC26A2c.1975T>G (p.Leu659Val)
c.372+3217T>G (n.372+3217T>G)
5g.149981569T>ACA361709551SLC26A2c.1976T>A (p.Leu659Ter)
c.372+3218T>A (n.372+3218T>A)
5g.149981569T>CCA361709553SLC26A2c.1976T>C (p.Leu659Ser)
c.372+3218T>C (n.372+3218T>C)
5g.149981569T>GCA361709552SLC26A2c.1976T>G (p.Leu659Ter)
c.372+3218T>G (n.372+3218T>G)
5g.149981570A>CCA361709554SLC26A2c.1977A>C (p.Leu659Phe)
c.372+3219A>C (n.372+3219A>C)
5g.149981570A>GCA447402967SLC26A2c.1977A>G (p.Leu659=)
c.372+3219A>G (n.372+3219A>G)
5g.149981570A>TCA361709555SLC26A2c.1977A>T (p.Leu659Phe)
c.372+3219A>T (n.372+3219A>T)
5g.149981570_149981571insATCA2531784885SLC26A2c.1977_1978insAT (p.Asp660MetfsTer9)
c.372+3219_372+3220insAT (n.372+3219_372+3220insAT)
5g.149981571G>ACA361709556SLC26A2c.1978G>A (p.Asp660Asn)
c.372+3220G>A (n.372+3220G>A)
5g.149981571G>CCA361709557SLC26A2c.1978G>C (p.Asp660His)
c.372+3220G>C (n.372+3220G>C)
5g.149981571G>TCA361709558SLC26A2c.1978G>T (p.Asp660Tyr)
c.372+3220G>T (n.372+3220G>T)
5g.149981572A=CA1590738832SLC26A2c.1979A= (p.Asp660=)
c.372+3221A= (n.372+3221A=)
5g.149981572A>CCA361709559SLC26A2c.1979A>C (p.Asp660Ala)
c.372+3221A>C (n.372+3221A>C)
5g.149981572A>GCA3505524SLC26A2c.1979A>G (p.Asp660Gly)
c.372+3221A>G (n.372+3221A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.149981572A>TCA361709560SLC26A2c.1979A>T (p.Asp660Val)
c.372+3221A>T (n.372+3221A>T)
5g.149981573T>ACA361709561SLC26A2c.1980T>A (p.Asp660Glu)
c.372+3222T>A (n.372+3222T>A)
5g.149981573T>CCA447402968SLC26A2c.1980T>C (p.Asp660=)
c.372+3222T>C (n.372+3222T>C)
ClinVar dbSNP
5g.149981573T>GCA361709562SLC26A2c.1980T>G (p.Asp660Glu)
c.372+3222T>G (n.372+3222T>G)
5g.149981574A>CCA361709563SLC26A2c.1981A>C (p.Thr661Pro)
c.372+3223A>C (n.372+3223A>C)
5g.149981574A>GCA361709565SLC26A2c.1981A>G (p.Thr661Ala)
c.372+3223A>G (n.372+3223A>G)
gnomAD v4
5g.149981574A>TCA361709564SLC26A2c.1981A>T (p.Thr661Ser)
c.372+3223A>T (n.372+3223A>T)
5g.149981574_149981575delinsACCA1590738833SLC26A2c.1981_1982delinsAC (p.Thr661=)
c.372+3223_372+3224delinsAC (n.372+3223_372+3224delinsAC)
5g.149981575delCA3505525SLC26A2c.1982del (p.Thr661LysfsTer7)
c.372+3224del (n.372+3224del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
5g.149981575C>ACA361709566SLC26A2c.1982C>A (p.Thr661Lys)
c.372+3224C>A (n.372+3224C>A)
5g.149981575C>GCA361709567SLC26A2c.1982C>G (p.Thr661Arg)
c.372+3224C>G (n.372+3224C>G)
5g.149981575C>TCA361709568SLC26A2c.1982C>T (p.Thr661Ile)
c.372+3224C>T (n.372+3224C>T)
dbSNP gnomAD v3 gnomAD v4
5g.149981575_149981576delinsCACA1590738834SLC26A2c.1982_1983delinsCA (p.Thr661=)
c.372+3224_372+3225delinsCA (n.372+3224_372+3225delinsCA)
5g.149981576delCA263257SLC26A2c.1983del (p.Ala662GlnfsTer6)
c.372+3225del (n.372+3225del)
ClinVar dbSNP
5g.149981576A>CCA447402969SLC26A2c.1983A>C (p.Thr661=)
c.372+3225A>C (n.372+3225A>C)
5g.149981576A>GCA447402970SLC26A2c.1983A>G (p.Thr661=)
c.372+3225A>G (n.372+3225A>G)
5g.149981576A>TCA447402971SLC26A2c.1983A>T (p.Thr661=)
c.372+3225A>T (n.372+3225A>T)
5g.149981577G>ACA361709571SLC26A2c.1984G>A (p.Ala662Thr)
c.372+3226G>A (n.372+3226G>A)
5g.149981577G>CCA361709570SLC26A2c.1984G>C (p.Ala662Pro)
c.372+3226G>C (n.372+3226G>C)
5g.149981577G>TCA361709569SLC26A2c.1984G>T (p.Ala662Ser)
c.372+3226G>T (n.372+3226G>T)
5g.149981578C>ACA361709572SLC26A2c.1985C>A (p.Ala662Glu)
c.372+3227C>A (n.372+3227C>A)
5g.149981578C=CA1590738835SLC26A2c.1985C= (p.Ala662=)
c.372+3227C= (n.372+3227C=)
5g.149981578C>GCA129084776SLC26A2c.1985C>G (p.Ala662Gly)
c.372+3227C>G (n.372+3227C>G)
dbSNP
5g.149981578C>TCA361709573SLC26A2c.1985C>T (p.Ala662Val)
c.372+3227C>T (n.372+3227C>T)
dbSNP gnomAD v2 gnomAD v4
5g.149981579A>CCA447402972SLC26A2c.1986A>C (p.Ala662=)
c.372+3228A>C (n.372+3228A>C)
gnomAD v4
5g.149981579A>GCA447402973SLC26A2c.1986A>G (p.Ala662=)
c.372+3228A>G (n.372+3228A>G)
dbSNP
5g.149981579A>TCA447402974SLC26A2c.1986A>T (p.Ala662=)
c.372+3228A>T (n.372+3228A>T)
5g.149981580G>ACA361709574SLC26A2c.1987G>A (p.Gly663Arg)
c.372+3229G>A (n.372+3229G>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
5g.149981580G>CCA361709575SLC26A2c.1987G>C (p.Gly663Arg)
c.372+3229G>C (n.372+3229G>C)
5g.149981580G=CA1590738836SLC26A2c.1987G= (p.Gly663=)
c.372+3229G= (n.372+3229G=)
5g.149981580G>TCA361709576SLC26A2c.1987G>T (p.Gly663Trp)
c.372+3229G>T (n.372+3229G>T)
5g.149981581G>ACA361709579SLC26A2c.1988G>A (p.Gly663Glu)
c.372+3230G>A (n.372+3230G>A)
5g.149981581G>CCA361709577SLC26A2c.1988G>C (p.Gly663Ala)
c.372+3230G>C (n.372+3230G>C)
5g.149981581G>TCA361709578SLC26A2c.1988G>T (p.Gly663Val)
c.372+3230G>T (n.372+3230G>T)
5g.149981582G>ACA447402977SLC26A2c.1989G>A (p.Gly663=)
c.372+3231G>A (n.372+3231G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
5g.149981582G>CCA447402976SLC26A2c.1989G>C (p.Gly663=)
c.372+3231G>C (n.372+3231G>C)
5g.149981582G=CA1590738837SLC26A2c.1989G= (p.Gly663=)
c.372+3231G= (n.372+3231G=)
5g.149981582G>TCA447402975SLC26A2c.1989G>T (p.Gly663=)
c.372+3231G>T (n.372+3231G>T)
5g.149981583A>CCA361709580SLC26A2c.1990A>C (p.Ile664Leu)
c.372+3232A>C (n.372+3232A>C)
5g.149981583A>GCA361709581SLC26A2c.1990A>G (p.Ile664Val)
c.372+3232A>G (n.372+3232A>G)
5g.149981583A>TCA361709582SLC26A2c.1990A>T (p.Ile664Phe)
c.372+3232A>T (n.372+3232A>T)
5g.149981584T>ACA361709583SLC26A2c.1991T>A (p.Ile664Asn)
c.372+3233T>A (n.372+3233T>A)
5g.149981584T>CCA361709584SLC26A2c.1991T>C (p.Ile664Thr)
c.372+3233T>C (n.372+3233T>C)
dbSNP gnomAD v2 gnomAD v4
5g.149981584T>GCA361709585SLC26A2c.1991T>G (p.Ile664Ser)
c.372+3233T>G (n.372+3233T>G)
5g.149981584T=CA1590738838SLC26A2c.1991T= (p.Ile664=)
c.372+3233T= (n.372+3233T=)

Number of alleles fetched