| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.101427574C>G | CA339810 | ALDOB | c.448G>C (p.Ala150Pro) n.68-936G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.101427574C>T | CA374265342 | ALDOB | c.448G>A (p.Ala150Thr) n.68-936G>A | dbSNP gnomAD v4 |
| 9 | g.101427574C= | CA1868280104 | ALDOB | c.448G= (p.Ala150=) n.68-936G= | dbSNP |