| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.107690238G>A | CA16041109 | SLC26A4 | c.1263+1G>A (n.1263+1G>A) | ClinVar dbSNP gnomAD v4 |
| 7 | g.107690238G>T | CA16041110 | SLC26A4 | c.1263+1G>T (n.1263+1G>T) | ClinVar dbSNP |
| 7 | g.107690238G= | CA1732748510 | SLC26A4 | c.1263+1G= (n.1263+1G=) | dbSNP |