| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28027236T>A | CA16602566 | FLT3 | c.2059A>T (p.Ile687Phe) n.2141A>T c.2002A>T (p.Ile668Phe) c.1534A>T (p.Ile512Phe) c.1843A>T (p.Ile615Phe) c.1180A>T (p.Ile394Phe) c.1162A>T (p.Ile388Phe) n.2125A>T | ClinVar dbSNP |
| 13 | g.28027236T>C | CA387652061 | FLT3 | c.2059A>G (p.Ile687Val) n.2141A>G c.2002A>G (p.Ile668Val) c.1534A>G (p.Ile512Val) c.1843A>G (p.Ile615Val) c.1180A>G (p.Ile394Val) c.1162A>G (p.Ile388Val) n.2125A>G | dbSNP gnomAD v2 gnomAD v4 |