| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28767840C>A | CA204685 | FOXG1 | c.561C>A (p.Asn187Lys) | ClinVar dbSNP |
| 14 | g.28767840C>G | CA10588574 | FOXG1 | c.561C>G (p.Asn187Lys) | ClinVar dbSNP |
| 14 | g.28767840C= | CA2125999767 | FOXG1 | c.561C= (p.Asn187=) | dbSNP |