| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.107663427C>T | CA4432413 | SLC26A4 | c.296C>T (p.Thr99Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 7 | g.107663427C>A | CA164209206 | SLC26A4 | c.296C>A (p.Thr99Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.107663427C>G | CA16616708 | SLC26A4 | c.296C>G (p.Thr99Arg) | ClinVar dbSNP |
| 7 | g.107663427C= | CA1732736234 | SLC26A4 | c.296C= (p.Thr99=) | dbSNP |