Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.128485741G>C | CA354405115 | GATA2 | c.857C>G (p.Ala286Gly) c.1139C>G (p.Ala380Gly) | ClinVar dbSNP |
3 | g.128485741G>A | CA207231 | GATA2 | c.857C>T (p.Ala286Val) c.1139C>T (p.Ala380Val) | ClinVar dbSNP |
3 | g.128485741G= | CA1400718892 | GATA2 | c.857C= (p.Ala286=) c.1139C= (p.Ala380=) | dbSNP |
3 | g.128485741G>T | CA354405116 | GATA2 | c.857C>A (p.Ala286Asp) c.1139C>A (p.Ala380Asp) | dbSNP gnomAD v4 |