| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 8 | g.11748963G>A | CA210836 | GATA4 | c.661G>A (p.Gly221Arg) c.664G>A (p.Gly222Arg) c.43G>A (p.Gly15Arg) c.658G>A (p.Gly220Arg) | ClinVar dbSNP |
| 8 | g.11748963G= | CA1764079660 | GATA4 | c.661G= (p.Gly221=) c.664G= (p.Gly222=) c.43G= (p.Gly15=) c.658G= (p.Gly220=) | dbSNP |