| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28768479C>A | CA235611 | FOXG1 | c.1200C>A (p.Tyr400Ter) | ClinVar dbSNP |
| 14 | g.28768479C>G | CA123557 | FOXG1 | c.1200C>G (p.Tyr400Ter) | ClinVar dbSNP |
| 14 | g.28768479C>T | CA7140671 | FOXG1 | c.1200C>T (p.Tyr400=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768479C= | CA2126000435 | FOXG1 | c.1200C= (p.Tyr400=) | dbSNP |