| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.1220694C>G | CA16608016 | STK11 | c.711C>G (p.Asp237Glu) c.339C>G (p.Asp113Glu) c.537C>G (p.Asp179Glu) n.609C>G n.801C>G n.682C>G c.489C>G (p.Asp163Glu) n.1336C>G | ClinVar dbSNP |
| 19 | g.1220694C>A | CA402949910 | STK11 | c.711C>A (p.Asp237Glu) c.339C>A (p.Asp113Glu) c.537C>A (p.Asp179Glu) n.609C>A n.801C>A n.682C>A c.489C>A (p.Asp163Glu) n.1336C>A | ClinVar dbSNP |
| 19 | g.1220694C>T | CA504892287 | STK11 | c.711C>T (p.Asp237=) c.339C>T (p.Asp113=) c.537C>T (p.Asp179=) n.609C>T n.801C>T n.682C>T c.489C>T (p.Asp163=) n.1336C>T | dbSNP |