| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.107674963C>T | CA16041104 | SLC26A4 | c.619C>T (p.Gln207Ter) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 7 | g.107674963C>G | CA368831026 | SLC26A4 | c.619C>G (p.Gln207Glu) | dbSNP |
| 7 | g.107674963C= | CA1732746894 | SLC26A4 | c.619C= (p.Gln207=) | dbSNP |