| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.2172367C>T | CA13370133 | TH | c.-581G>A (n.-581G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.2172367C>A | CA1948012874 | TH | c.-581G>T (n.-581G>T) | dbSNP |
| 11 | g.2172367C>G | CA1948012875 | TH | c.-581G>C (n.-581G>C) | dbSNP |