| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.77794572T>A | CA16602434 | GNAQ | c.626A>T (p.Gln209Leu) c.452A>T (p.Gln151Leu) | ClinVar dbSNP COSMIC |
| 9 | g.77794572T>G | CA16602436 | GNAQ | c.626A>C (p.Gln209Pro) c.452A>C (p.Gln151Pro) | ClinVar dbSNP COSMIC |
| 9 | g.77794572T>C | CA16602435 | GNAQ | c.626A>G (p.Gln209Arg) c.452A>G (p.Gln151Arg) | ClinVar dbSNP COSMIC |