| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.1220395G>C | CA023047 | STK11 | c.487G>C (p.Gly163Arg) c.115G>C (p.Gly39Arg) c.313G>C (p.Gly105Arg) n.310G>C n.577G>C n.383G>C c.265G>C (p.Gly89Arg) n.1112G>C | ClinVar dbSNP |
| 19 | g.1220395G>A | CA089408 | STK11 | c.487G>A (p.Gly163Ser) c.115G>A (p.Gly39Ser) c.313G>A (p.Gly105Ser) n.310G>A n.577G>A n.383G>A c.265G>A (p.Gly89Ser) n.1112G>A | dbSNP gnomAD v4 |
| 19 | g.1220395G>T | CA16603120 | STK11 | c.487G>T (p.Gly163Cys) c.115G>T (p.Gly39Cys) c.313G>T (p.Gly105Cys) n.310G>T n.577G>T n.383G>T c.265G>T (p.Gly89Cys) n.1112G>T | ClinVar dbSNP gnomAD v4 COSMIC |