| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.1220396G>A | CA023051 | STK11 | c.488G>A (p.Gly163Asp) c.116G>A (p.Gly39Asp) c.314G>A (p.Gly105Asp) n.311G>A n.578G>A n.384G>A c.266G>A (p.Gly89Asp) n.1113G>A | ClinVar dbSNP gnomAD v4 COSMIC |
| 19 | g.1220396G>C | CA402948852 | STK11 | c.488G>C (p.Gly163Ala) c.116G>C (p.Gly39Ala) c.314G>C (p.Gly105Ala) n.311G>C n.578G>C n.384G>C c.266G>C (p.Gly89Ala) n.1113G>C | dbSNP |