| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.1806476T>C | CA16617026 | GNB1 | c.227A>G (p.Lys76Arg) c.-35A>G (n.-35A>G) c.266A>G (p.Lys89Arg) c.134A>G (p.Lys45Arg) n.870A>G | ClinVar dbSNP gnomAD v4 |
| 1 | g.1806476T>A | CA337916155 | GNB1 | c.227A>T (p.Lys76Met) c.-35A>T (n.-35A>T) c.266A>T (p.Lys89Met) c.134A>T (p.Lys45Met) n.870A>T | ClinVar dbSNP |