| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.5227019C>T | CA125383 | HBB | c.3G>A (p.Met1Ile) n.54G>A | ClinVar dbSNP |
| 11 | g.5227019C>G | CA217115643 | HBB | c.3G>C (p.Met1Ile) n.54G>C | ClinVar dbSNP |
| 11 | g.5227019C>A | CA217115639 | HBB | c.3G>T (p.Met1Ile) n.54G>T | ClinVar dbSNP |