| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.133777112A>G | CA122565 | TF | c.1936A>G (p.Lys646Glu) c.667A>G n.2930A>G c.1804A>G (p.Lys602Glu) c.1555A>G (p.Lys519Glu) | ClinVar dbSNP |
| 3 | g.133777112A= | CA1403124845 | TF | c.1936A= (p.Lys646=) c.667A= n.2930A= c.1804A= (p.Lys602=) c.1555A= (p.Lys519=) | dbSNP |