Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28768044G>A | CA123550 | FOXG1 | c.765G>A (p.Trp255Ter) | ClinVar dbSNP |
14 | g.28768044G>T | CA172197 | FOXG1 | c.765G>T (p.Trp255Cys) | ClinVar dbSNP |
14 | g.28768044G>C | CA389475821 | FOXG1 | c.765G>C (p.Trp255Cys) | ClinVar dbSNP |
14 | g.28768044G= | CA2126000188 | FOXG1 | c.765G= (p.Trp255=) | dbSNP |