| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.1220495G>T | CA16602779 | STK11 | c.587G>T (p.Gly196Val) c.215G>T (p.Gly72Val) c.413G>T (p.Gly138Val) n.410G>T n.677G>T n.483G>T c.365G>T (p.Gly122Val) n.1212G>T | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
| 19 | g.1220495G>C | CA402949289 | STK11 | c.587G>C (p.Gly196Ala) c.215G>C (p.Gly72Ala) c.413G>C (p.Gly138Ala) n.410G>C n.677G>C n.483G>C c.365G>C (p.Gly122Ala) n.1212G>C | ClinVar dbSNP |
| 19 | g.1220495G>A | CA402949286 | STK11 | c.587G>A (p.Gly196Asp) c.215G>A (p.Gly72Asp) c.413G>A (p.Gly138Asp) n.410G>A n.677G>A n.483G>A c.365G>A (p.Gly122Asp) n.1212G>A | ClinVar dbSNP gnomAD v4 |