| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.177362A>T | CA125933 | HBA1 | c.380A>T (p.Asp127Val) c.284A>T (p.Asp95Val) n.516A>T | ClinVar dbSNP |
| 16 | g.177362A>G | CA276417209 | HBA1 | c.380A>G (p.Asp127Gly) c.284A>G (p.Asp95Gly) n.516A>G | dbSNP |
| 16 | g.177362A>C | CA276417205 | HBA1 | c.380A>C (p.Asp127Ala) c.284A>C (p.Asp95Ala) n.516A>C | dbSNP |
| 16 | g.177362A= | CA2200883287 | HBA1 | c.380A= (p.Asp127=) c.284A= (p.Asp95=) n.516A= | dbSNP |