| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 18 | g.11881049G>A | CA16620660 | GNAL | c.1291G>A (p.Val431Met) c.1060G>A (p.Val354Met) c.439G>A (p.Val147Met) | ClinVar dbSNP COSMIC |
| 18 | g.11881049G= | CA2284983272 | GNAL | c.1291G= (p.Val431=) c.1060G= (p.Val354=) c.439G= (p.Val147=) | dbSNP |