Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28767833G>T | CA10654909 | FOXG1 | c.554G>T (p.Ser185Ile) | ClinVar dbSNP |
14 | g.28767833G>C | CA389475349 | FOXG1 | c.554G>C (p.Ser185Thr) | ClinVar dbSNP |
14 | g.28767833G= | CA2125999756 | FOXG1 | c.554G= (p.Ser185=) | dbSNP |