Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
21 | g.34880598G>T | CA248628 | RUNX1 | c.467C>A (p.Ala156Glu) c.386C>A (p.Ala129Glu) c.431C>A (p.Ala144Glu) c.*57C>A (n.*57C>A) c.428C>A (p.Ala143Glu) n.646C>A c.314C>A (p.Ala105Glu) n.693C>A | ClinVar dbSNP |
21 | g.34880598G>A | CA410202550 | RUNX1 | c.467C>T (p.Ala156Val) c.386C>T (p.Ala129Val) c.431C>T (p.Ala144Val) c.*57C>T (n.*57C>T) c.428C>T (p.Ala143Val) n.646C>T c.314C>T (p.Ala105Val) n.693C>T | dbSNP |
21 | g.34880598G>C | CA410202551 | RUNX1 | c.467C>G (p.Ala156Gly) c.386C>G (p.Ala129Gly) c.431C>G (p.Ala144Gly) c.*57C>G (n.*57C>G) c.428C>G (p.Ala143Gly) n.646C>G c.314C>G (p.Ala105Gly) n.693C>G | dbSNP |