Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.128481901G>A | CA128580 | GATA2 | c.1061C>T (p.Thr354Met) c.1343C>T (p.Thr448Met) c.44C>T (p.Thr15Met) c.1019C>T (p.Thr340Met) n.178C>T | ClinVar dbSNP gnomAD v4 COSMIC |
3 | g.128481901G>C | CA354413617 | GATA2 | c.1061C>G (p.Thr354Arg) c.1343C>G (p.Thr448Arg) c.44C>G (p.Thr15Arg) c.1019C>G (p.Thr340Arg) n.178C>G | ClinVar dbSNP gnomAD v4 COSMIC |