| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.186620636A>C | CA2745044 | AHSG | c.810A>C (p.Thr270=) c.813A>C (p.Thr271=) c.807A>C (p.Thr269=) c.726A>C (p.Thr242=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.186620636A>G | CA437358351 | AHSG | c.810A>G (p.Thr270=) c.813A>G (p.Thr271=) c.807A>G (p.Thr269=) c.726A>G (p.Thr242=) | dbSNP |