| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.1220700G>C | CA023239 | STK11 | c.717G>C (p.Trp239Cys) c.345G>C (p.Trp115Cys) c.543G>C (p.Trp181Cys) n.615G>C n.807G>C n.688G>C c.495G>C (p.Trp165Cys) n.1342G>C | ClinVar dbSNP |
| 19 | g.1220700G>T | CA402949935 | STK11 | c.717G>T (p.Trp239Cys) c.345G>T (p.Trp115Cys) c.543G>T (p.Trp181Cys) n.615G>T n.807G>T n.688G>T c.495G>T (p.Trp165Cys) n.1342G>T | ClinVar dbSNP COSMIC COSMIC |
| 19 | g.1220700G>A | CA10603426 | STK11 | c.717G>A (p.Trp239Ter) c.345G>A (p.Trp115Ter) c.543G>A (p.Trp181Ter) n.615G>A n.807G>A n.688G>A c.495G>A (p.Trp165Ter) n.1342G>A | ClinVar dbSNP |