| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.41568689C>T | CA12323515 | FOXP4 | c.204+2725C>T (n.204+2725C>T) n.545+2725C>T n.546+2725C>T n.543+2725C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.41568689C>G | CA1623676416 | FOXP4 | c.204+2725C>G (n.204+2725C>G) n.545+2725C>G n.546+2725C>G n.543+2725C>G | dbSNP |