| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.55269449T>C | CA12388350 | HCRTR2 | c.762+5627T>C (n.762+5627T>C) c.567+5627T>C (n.567+5627T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.55269449T>G | CA2581586458 | HCRTR2 | c.762+5627T>G (n.762+5627T>G) c.567+5627T>G (n.567+5627T>G) | dbSNP |