| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.1220435A>C | CA402949012 | STK11 | c.527A>C (p.Asp176Ala) c.155A>C (p.Asp52Ala) c.353A>C (p.Asp118Ala) n.350A>C n.617A>C n.423A>C c.305A>C (p.Asp102Ala) n.1152A>C | ClinVar dbSNP COSMIC COSMIC |
| 19 | g.1220435A>T | CA402949014 | STK11 | c.527A>T (p.Asp176Val) c.155A>T (p.Asp52Val) c.353A>T (p.Asp118Val) n.350A>T n.617A>T n.423A>T c.305A>T (p.Asp102Val) n.1152A>T | dbSNP |
| 19 | g.1220435A>G | CA16620748 | STK11 | c.527A>G (p.Asp176Gly) c.155A>G (p.Asp52Gly) c.353A>G (p.Asp118Gly) n.350A>G n.617A>G n.423A>G c.305A>G (p.Asp102Gly) n.1152A>G | ClinVar dbSNP |