| 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 |
| 3 | g.186620636A= | CA1427019577 | AHSG | c.810A= (p.Thr270=) c.813A= (p.Thr271=) c.807A= (p.Thr269=) c.726A= (p.Thr242=) | dbSNP dbSNP |
| 3 | g.186620636A>T | CA437358352 | AHSG | c.810A>T (p.Thr270=) c.813A>T (p.Thr271=) c.807A>T (p.Thr269=) c.726A>T (p.Thr242=) | dbSNP gnomAD v4 |