| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28767685G>T | CA16606550 | FOXG1 | c.406G>T (p.Glu136Ter) | ClinVar dbSNP |
| 14 | g.28767685G>A | CA389475028 | FOXG1 | c.406G>A (p.Glu136Lys) | dbSNP gnomAD v4 |
| 14 | g.28767685G= | CA2125999349 | FOXG1 | c.406G= (p.Glu136=) | dbSNP |