| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28767922T>C | CA123554 | FOXG1 | c.643T>C (p.Phe215Leu) | ClinVar dbSNP |
| 14 | g.28767922T>A | CA389475554 | FOXG1 | c.643T>A (p.Phe215Ile) | ClinVar dbSNP |
| 14 | g.28767922T= | CA2125999890 | FOXG1 | c.643T= (p.Phe215=) | dbSNP |