Chr Mutation (hg38) CAid Gene Transcript Linkouts
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)

Number of alleles fetched