| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.107674350T>A | CA16041103 | SLC26A4 | c.600+2T>A (n.600+2T>A) | ClinVar dbSNP |
| 7 | g.107674350T>C | CA368848470 | SLC26A4 | c.600+2T>C (n.600+2T>C) | ClinVar dbSNP |
| 7 | g.107674350T= | CA1732746321 | SLC26A4 | c.600+2T= (n.600+2T=) | dbSNP |