Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.128481270G>A | CA128572 | GATA2 | c.1192C>T (p.Arg398Trp) c.1474C>T (p.Arg492Trp) c.167C>T (p.Pro56Leu) c.1150C>T (p.Arg384Trp) n.309C>T | ClinVar dbSNP gnomAD v4 COSMIC |
3 | g.128481270G>C | CA354413214 | GATA2 | c.1192C>G (p.Arg398Gly) c.1474C>G (p.Arg492Gly) c.167C>G (p.Pro56Arg) c.1150C>G (p.Arg384Gly) n.309C>G | ClinVar dbSNP |
3 | g.128481270G= | CA1400714294 | GATA2 | c.1192C= (p.Arg398=) c.1474C= (p.Arg492=) c.167C= (p.Pro56=) c.1150C= (p.Arg384=) n.309C= | dbSNP |