| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.5225633C>G | CA125500 | HBB | c.409G>C (p.Gly137Arg) c.*225G>C (n.*225G>C) | ClinVar dbSNP |
| 11 | g.5225633C>T | CA217112357 | HBB | c.409G>A (p.Gly137Ser) c.*225G>A (n.*225G>A) | dbSNP |
| 11 | g.5225633C>A | CA217112360 | HBB | c.409G>T (p.Gly137Cys) c.*225G>T (n.*225G>T) | dbSNP |