| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28767903C>G | CA123552 | FOXG1 | c.624C>G (p.Tyr208Ter) | ClinVar dbSNP |
| 14 | g.28767903C>A | CA389475504 | FOXG1 | c.624C>A (p.Tyr208Ter) | ClinVar dbSNP |
| 14 | g.28767903C>T | CA7140622 | FOXG1 | c.624C>T (p.Tyr208=) | ClinVar dbSNP ExAC gnomAD v2 |
| 14 | g.28767903C= | CA2125999869 | FOXG1 | c.624C= (p.Tyr208=) | dbSNP |