| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.1221216C>G | CA023261 | STK11 | c.738C>G (p.Tyr246Ter) c.366C>G (p.Tyr122Ter) c.564C>G (p.Tyr188Ter) n.636C>G n.828C>G n.709C>G c.516C>G (p.Tyr172Ter) n.1363C>G | ClinVar dbSNP |
| 19 | g.1221216C>T | CA16608829 | STK11 | c.738C>T (p.Tyr246=) c.366C>T (p.Tyr122=) c.564C>T (p.Tyr188=) n.636C>T n.828C>T n.709C>T c.516C>T (p.Tyr172=) n.1363C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |