| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.5226996T>G | CA130022 | HBB | c.26A>C (p.Lys9Thr) n.77A>C | ClinVar dbSNP |
| 11 | g.5226996T>C | CA125468 | HBB | c.26A>G (p.Lys9Arg) n.77A>G | ClinVar dbSNP |
| 11 | g.5226996T>A | CA125428 | HBB | c.26A>T (p.Lys9Met) n.77A>T | ClinVar dbSNP |
| 11 | g.5226996T= | CA1949570971 | HBB | c.26A= (p.Lys9=) n.77A= | dbSNP |