Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107767771_107767772delCA2777358104SLC26A3c.2199_2200del (p.Gln735GlyfsTer7)
c.*1756_*1757del (n.*1756_*1757del)
7g.107767772G>ACA457205853SLC26A3c.2199C>T (p.Pro733=)
c.*1756C>T (n.*1756C>T)
7g.107767772G>CCA457205855SLC26A3c.2199C>G (p.Pro733=)
c.*1756C>G (n.*1756C>G)
7g.107767772G>TCA457205856SLC26A3c.2199C>A (p.Pro733=)
c.*1756C>A (n.*1756C>A)
7g.107767773G>ACA4433557SLC26A3c.2198C>T (p.Pro733Leu)
c.*1755C>T (n.*1755C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.107767773G>CCA368849511SLC26A3c.2198C>G (p.Pro733Arg)
c.*1755C>G (n.*1755C>G)
7g.107767773G=CA1732790143SLC26A3c.2198C= (p.Pro733=)
c.*1755C= (n.*1755C=)
7g.107767773G>TCA368849512SLC26A3c.2198C>A (p.Pro733His)
c.*1755C>A (n.*1755C>A)
7g.107767774G>ACA368849513SLC26A3c.2197C>T (p.Pro733Ser)
c.*1754C>T (n.*1754C>T)
7g.107767774G>CCA368849514SLC26A3c.2197C>G (p.Pro733Ala)
c.*1754C>G (n.*1754C>G)
7g.107767774G>TCA368849515SLC26A3c.2197C>A (p.Pro733Thr)
c.*1754C>A (n.*1754C>A)
dbSNP
7g.107767775A>CCA368849516SLC26A3c.2196T>G (p.Asn732Lys)
c.*1753T>G (n.*1753T>G)
7g.107767775A>GCA457205861SLC26A3c.2196T>C (p.Asn732=)
c.*1753T>C (n.*1753T>C)
7g.107767775A>TCA368849517SLC26A3c.2196T>A (p.Asn732Lys)
c.*1753T>A (n.*1753T>A)
7g.107767776T>ACA368849519SLC26A3c.2195A>T (p.Asn732Ile)
c.*1752A>T (n.*1752A>T)
7g.107767776T>CCA368849520SLC26A3c.2195A>G (p.Asn732Ser)
c.*1752A>G (n.*1752A>G)
7g.107767776T>GCA368849518SLC26A3c.2195A>C (p.Asn732Thr)
c.*1752A>C (n.*1752A>C)
7g.107767777T>ACA368849523SLC26A3c.2194A>T (p.Asn732Tyr)
c.*1751A>T (n.*1751A>T)
7g.107767777T>CCA368849521SLC26A3c.2194A>G (p.Asn732Asp)
c.*1751A>G (n.*1751A>G)
7g.107767777T>GCA368849522SLC26A3c.2194A>C (p.Asn732His)
c.*1751A>C (n.*1751A>C)
7g.107767778A=CA1732790147SLC26A3c.2193T= (p.Phe731=)
c.*1750T= (n.*1750T=)
7g.107767778A>CCA368849524SLC26A3c.2193T>G (p.Phe731Leu)
c.*1750T>G (n.*1750T>G)
dbSNP gnomAD v4
7g.107767778A>GCA4433558SLC26A3c.2193T>C (p.Phe731=)
c.*1750T>C (n.*1750T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107767778A>TCA368849525SLC26A3c.2193T>A (p.Phe731Leu)
c.*1750T>A (n.*1750T>A)
7g.107767779A>CCA368849526SLC26A3c.2192T>G (p.Phe731Cys)
c.*1749T>G (n.*1749T>G)
7g.107767779A>GCA368849527SLC26A3c.2192T>C (p.Phe731Ser)
c.*1749T>C (n.*1749T>C)
7g.107767779A>TCA368849528SLC26A3c.2192T>A (p.Phe731Tyr)
c.*1749T>A (n.*1749T>A)
7g.107767780A>CCA368849529SLC26A3c.2191T>G (p.Phe731Val)
c.*1748T>G (n.*1748T>G)
7g.107767780A>GCA368849530SLC26A3c.2191T>C (p.Phe731Leu)
c.*1748T>C (n.*1748T>C)
7g.107767780A>TCA368849531SLC26A3c.2191T>A (p.Phe731Ile)
c.*1748T>A (n.*1748T>A)
7g.107767781C>ACA368849532SLC26A3c.2190G>T (p.Lys730Asn)
c.*1747G>T (n.*1747G>T)
7g.107767781C>GCA368849533SLC26A3c.2190G>C (p.Lys730Asn)
c.*1747G>C (n.*1747G>C)
ClinVar gnomAD v4
7g.107767781C>TCA457205869SLC26A3c.2190G>A (p.Lys730=)
c.*1747G>A (n.*1747G>A)
gnomAD v4
7g.107767782T>ACA368849534SLC26A3c.2189A>T (p.Lys730Met)
c.*1746A>T (n.*1746A>T)
7g.107767782T>CCA368849536SLC26A3c.2189A>G (p.Lys730Arg)
c.*1746A>G (n.*1746A>G)
7g.107767782T>GCA368849535SLC26A3c.2189A>C (p.Lys730Thr)
c.*1746A>C (n.*1746A>C)
7g.107767783T>ACA368849537SLC26A3c.2188A>T (p.Lys730Ter)
c.*1745A>T (n.*1745A>T)
7g.107767783T>CCA368849538SLC26A3c.2188A>G (p.Lys730Glu)
c.*1745A>G (n.*1745A>G)
dbSNP gnomAD v2 gnomAD v4
7g.107767783T>GCA368849539SLC26A3c.2188A>C (p.Lys730Gln)
c.*1745A>C (n.*1745A>C)
7g.107767783T=CA1732790150SLC26A3c.2188A= (p.Lys730=)
c.*1745A= (n.*1745A=)
7g.107767784T>ACA457205875SLC26A3c.2187A>T (p.Ser729=)
c.*1744A>T (n.*1744A>T)
7g.107767784T>CCA457205873SLC26A3c.2187A>G (p.Ser729=)
c.*1744A>G (n.*1744A>G)
dbSNP gnomAD v2 gnomAD v4
7g.107767784T>GCA457205874SLC26A3c.2187A>C (p.Ser729=)
c.*1744A>C (n.*1744A>C)
7g.107767784T=CA1732790151SLC26A3c.2187A= (p.Ser729=)
c.*1744A= (n.*1744A=)
7g.107767785G>ACA368849540SLC26A3c.2186C>T (p.Ser729Leu)
c.*1743C>T (n.*1743C>T)
7g.107767785G>CCA368849541SLC26A3c.2186C>G (p.Ser729Ter)
c.*1743C>G (n.*1743C>G)
7g.107767785G>TCA368849542SLC26A3c.2186C>A (p.Ser729Ter)
c.*1743C>A (n.*1743C>A)
7g.107767786A=CA1732790153SLC26A3c.2185T= (p.Ser729=)
c.*1742T= (n.*1742T=)
7g.107767786A>CCA368849543SLC26A3c.2185T>G (p.Ser729Ala)
c.*1742T>G (n.*1742T>G)
dbSNP gnomAD v2 gnomAD v4
7g.107767786A>GCA368849544SLC26A3c.2185T>C (p.Ser729Pro)
c.*1742T>C (n.*1742T>C)

Number of alleles fetched