| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.1220489A>C | CA402949263 | STK11 | c.581A>C (p.Asp194Ala) c.209A>C (p.Asp70Ala) c.407A>C (p.Asp136Ala) n.404A>C n.671A>C n.477A>C c.359A>C (p.Asp120Ala) n.1206A>C | dbSNP |
| 19 | g.1220489A>T | CA16602778 | STK11 | c.581A>T (p.Asp194Val) c.209A>T (p.Asp70Val) c.407A>T (p.Asp136Val) n.404A>T n.671A>T n.477A>T c.359A>T (p.Asp120Val) n.1206A>T | ClinVar dbSNP COSMIC |
| 19 | g.1220489A>G | CA402949265 | STK11 | c.581A>G (p.Asp194Gly) c.209A>G (p.Asp70Gly) c.407A>G (p.Asp136Gly) n.404A>G n.671A>G n.477A>G c.359A>G (p.Asp120Gly) n.1206A>G | dbSNP |