Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.107674269C>A | CA368848175 | SLC26A4 | c.521C>A (p.Thr174Asn) | |
7 | g.107674269C= | CA1732746071 | SLC26A4 | c.521C= (p.Thr174=) | |
7 | g.107674269C>G | CA10576711 | SLC26A4 | c.521C>G (p.Thr174Ser) | ClinVar dbSNP gnomAD v4 |
7 | g.107674269C>T | CA368848177 | SLC26A4 | c.521C>T (p.Thr174Ile) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.107674270T>A | CA457105402 | SLC26A4 | c.522T>A (p.Thr174=) | gnomAD v4 |
7 | g.107674270T>C | CA457105403 | SLC26A4 | c.522T>C (p.Thr174=) | ClinVar dbSNP gnomAD v2 |
7 | g.107674270T>G | CA4432500 | SLC26A4 | c.522T>G (p.Thr174=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.107674270T= | CA1732746074 | SLC26A4 | c.522T= (p.Thr174=) | |
7 | g.107674271A= | CA1732746079 | SLC26A4 | c.523A= (p.Met175=) | |
7 | g.107674271A>C | CA368848184 | SLC26A4 | c.523A>C (p.Met175Leu) | |
7 | g.107674271A>G | CA4432501 | SLC26A4 | c.523A>G (p.Met175Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107674271A>T | CA368848182 | SLC26A4 | c.523A>T (p.Met175Leu) | |
7 | g.107674272T>A | CA368848185 | SLC26A4 | c.524T>A (p.Met175Lys) | |
7 | g.107674272T>C | CA368848186 | SLC26A4 | c.524T>C (p.Met175Thr) | dbSNP gnomAD v4 |
7 | g.107674272T>G | CA368848187 | SLC26A4 | c.524T>G (p.Met175Arg) | |
7 | g.107674272T= | CA1732746083 | SLC26A4 | c.524T= (p.Met175=) | |
7 | g.107674273G>A | CA164216355 | SLC26A4 | c.525G>A (p.Met175Ile) | dbSNP COSMIC |
7 | g.107674273G>C | CA368848190 | SLC26A4 | c.525G>C (p.Met175Ile) | COSMIC |
7 | g.107674273G= | CA1732746084 | SLC26A4 | c.525G= (p.Met175=) | |
7 | g.107674273G>T | CA368848191 | SLC26A4 | c.525G>T (p.Met175Ile) | gnomAD v4 |
7 | g.107674274A>C | CA368848192 | SLC26A4 | c.526A>C (p.Ile176Leu) | |
7 | g.107674274A>G | CA368848193 | SLC26A4 | c.526A>G (p.Ile176Val) | |
7 | g.107674274A>T | CA368848194 | SLC26A4 | c.526A>T (p.Ile176Leu) | |
7 | g.107674275T>A | CA368848197 | SLC26A4 | c.527T>A (p.Ile176Lys) | |
7 | g.107674275T>C | CA4432502 | SLC26A4 | c.527T>C (p.Ile176Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107674275T>G | CA368848198 | SLC26A4 | c.527T>G (p.Ile176Arg) | |
7 | g.107674275T= | CA1732746092 | SLC26A4 | c.527T= (p.Ile176=) | |
7 | g.107674276A>C | CA457105404 | SLC26A4 | c.528A>C (p.Ile176=) | |
7 | g.107674276A>G | CA368848201 | SLC26A4 | c.528A>G (p.Ile176Met) | |
7 | g.107674276A>T | CA457105405 | SLC26A4 | c.528A>T (p.Ile176=) | |
7 | g.107674277G>A | CA368848206 | SLC26A4 | c.529G>A (p.Asp177Asn) | |
7 | g.107674277G>C | CA368848204 | SLC26A4 | c.529G>C (p.Asp177His) | |
7 | g.107674277G>T | CA368848203 | SLC26A4 | c.529G>T (p.Asp177Tyr) | |
7 | g.107674278A= | CA1732746095 | SLC26A4 | c.530A= (p.Asp177=) | |
7 | g.107674278A>C | CA368848208 | SLC26A4 | c.530A>C (p.Asp177Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107674278A>G | CA368848210 | SLC26A4 | c.530A>G (p.Asp177Gly) | |
7 | g.107674278A>T | CA368848211 | SLC26A4 | c.530A>T (p.Asp177Val) | |
7 | g.107674279C>A | CA368848212 | SLC26A4 | c.531C>A (p.Asp177Glu) | |
7 | g.107674279C= | CA1732746099 | SLC26A4 | c.531C= (p.Asp177=) | |
7 | g.107674279C>G | CA368848214 | SLC26A4 | c.531C>G (p.Asp177Glu) | |
7 | g.107674279C>T | CA457105406 | SLC26A4 | c.531C>T (p.Asp177=) | ClinVar dbSNP |
7 | g.107674280A= | CA1732746102 | SLC26A4 | c.532A= (p.Thr178=) | |
7 | g.107674280A>C | CA4432503 | SLC26A4 | c.532A>C (p.Thr178Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107674280A>G | CA368848215 | SLC26A4 | c.532A>G (p.Thr178Ala) | |
7 | g.107674280A>T | CA368848216 | SLC26A4 | c.532A>T (p.Thr178Ser) | |
7 | g.107674281C>A | CA368848217 | SLC26A4 | c.533C>A (p.Thr178Asn) | dbSNP |
7 | g.107674281C= | CA1732746105 | SLC26A4 | c.533C= (p.Thr178=) | |
7 | g.107674281C>G | CA368848219 | SLC26A4 | c.533C>G (p.Thr178Ser) | |
7 | g.107674281C>T | CA368848220 | SLC26A4 | c.533C>T (p.Thr178Ile) | COSMIC |
7 | g.107674282T>A | CA457105407 | SLC26A4 | c.534T>A (p.Thr178=) |