Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.107674269C>ACA368848175SLC26A4c.521C>A (p.Thr174Asn)
7g.107674269C=CA1732746071SLC26A4c.521C= (p.Thr174=)
7g.107674269C>GCA10576711SLC26A4c.521C>G (p.Thr174Ser)
ClinVar dbSNP gnomAD v4
7g.107674269C>TCA368848177SLC26A4c.521C>T (p.Thr174Ile)
dbSNP gnomAD v2 gnomAD v4
7g.107674270T>ACA457105402SLC26A4c.522T>A (p.Thr174=)
gnomAD v4
7g.107674270T>CCA457105403SLC26A4c.522T>C (p.Thr174=)
ClinVar dbSNP gnomAD v2
7g.107674270T>GCA4432500SLC26A4c.522T>G (p.Thr174=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.107674270T=CA1732746074SLC26A4c.522T= (p.Thr174=)
7g.107674271A=CA1732746079SLC26A4c.523A= (p.Met175=)
7g.107674271A>CCA368848184SLC26A4c.523A>C (p.Met175Leu)
7g.107674271A>GCA4432501SLC26A4c.523A>G (p.Met175Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107674271A>TCA368848182SLC26A4c.523A>T (p.Met175Leu)
7g.107674272T>ACA368848185SLC26A4c.524T>A (p.Met175Lys)
7g.107674272T>CCA368848186SLC26A4c.524T>C (p.Met175Thr)
dbSNP gnomAD v4
7g.107674272T>GCA368848187SLC26A4c.524T>G (p.Met175Arg)
7g.107674272T=CA1732746083SLC26A4c.524T= (p.Met175=)
7g.107674273G>ACA164216355SLC26A4c.525G>A (p.Met175Ile)
dbSNP COSMIC
7g.107674273G>CCA368848190SLC26A4c.525G>C (p.Met175Ile)
COSMIC
7g.107674273G=CA1732746084SLC26A4c.525G= (p.Met175=)
7g.107674273G>TCA368848191SLC26A4c.525G>T (p.Met175Ile)
gnomAD v4
7g.107674274A>CCA368848192SLC26A4c.526A>C (p.Ile176Leu)
7g.107674274A>GCA368848193SLC26A4c.526A>G (p.Ile176Val)
7g.107674274A>TCA368848194SLC26A4c.526A>T (p.Ile176Leu)
7g.107674275T>ACA368848197SLC26A4c.527T>A (p.Ile176Lys)
7g.107674275T>CCA4432502SLC26A4c.527T>C (p.Ile176Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107674275T>GCA368848198SLC26A4c.527T>G (p.Ile176Arg)
7g.107674275T=CA1732746092SLC26A4c.527T= (p.Ile176=)
7g.107674276A>CCA457105404SLC26A4c.528A>C (p.Ile176=)
7g.107674276A>GCA368848201SLC26A4c.528A>G (p.Ile176Met)
7g.107674276A>TCA457105405SLC26A4c.528A>T (p.Ile176=)
7g.107674277G>ACA368848206SLC26A4c.529G>A (p.Asp177Asn)
7g.107674277G>CCA368848204SLC26A4c.529G>C (p.Asp177His)
7g.107674277G>TCA368848203SLC26A4c.529G>T (p.Asp177Tyr)
7g.107674278A=CA1732746095SLC26A4c.530A= (p.Asp177=)
7g.107674278A>CCA368848208SLC26A4c.530A>C (p.Asp177Ala)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.107674278A>GCA368848210SLC26A4c.530A>G (p.Asp177Gly)
7g.107674278A>TCA368848211SLC26A4c.530A>T (p.Asp177Val)
7g.107674279C>ACA368848212SLC26A4c.531C>A (p.Asp177Glu)
7g.107674279C=CA1732746099SLC26A4c.531C= (p.Asp177=)
7g.107674279C>GCA368848214SLC26A4c.531C>G (p.Asp177Glu)
7g.107674279C>TCA457105406SLC26A4c.531C>T (p.Asp177=)
ClinVar dbSNP
7g.107674280A=CA1732746102SLC26A4c.532A= (p.Thr178=)
7g.107674280A>CCA4432503SLC26A4c.532A>C (p.Thr178Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.107674280A>GCA368848215SLC26A4c.532A>G (p.Thr178Ala)
7g.107674280A>TCA368848216SLC26A4c.532A>T (p.Thr178Ser)
7g.107674281C>ACA368848217SLC26A4c.533C>A (p.Thr178Asn)
dbSNP
7g.107674281C=CA1732746105SLC26A4c.533C= (p.Thr178=)
7g.107674281C>GCA368848219SLC26A4c.533C>G (p.Thr178Ser)
7g.107674281C>TCA368848220SLC26A4c.533C>T (p.Thr178Ile)
COSMIC
7g.107674282T>ACA457105407SLC26A4c.534T>A (p.Thr178=)

Number of alleles fetched