| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28767924C>A | CA389475558 | FOXG1 | c.645C>A (p.Phe215Leu) | ClinVar dbSNP |
| 14 | g.28767924C>T | CA486098527 | FOXG1 | c.645C>T (p.Phe215=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28767924C>G | CA16042954 | FOXG1 | c.645C>G (p.Phe215Leu) | ClinVar dbSNP |