| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.5226976A>C | CA125124 | HBB | c.46T>G (p.Trp16Gly) n.97T>G | ClinVar dbSNP |
| 11 | g.5226976A>G | CA217115404 | HBB | c.46T>C (p.Trp16Arg) n.97T>C | dbSNP |
| 11 | g.5226976A>T | CA124742 | HBB | c.46T>A (p.Trp16Arg) n.97T>A | ClinVar dbSNP |
| 11 | g.5226976A= | CA1949570728 | HBB | c.46T= (p.Trp16=) n.97T= | dbSNP dbSNP |