| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28018503A>T | CA16602449 | FLT3 | c.2505T>A (p.Asp835Glu) c.*417T>A (n.*417T>A) n.2719T>A c.2448T>A (p.Asp816Glu) c.1980T>A (p.Asp660Glu) c.2289T>A (p.Asp763Glu) c.1626T>A (p.Asp542Glu) c.1608T>A (p.Asp536Glu) n.2703T>A | ClinVar dbSNP |
| 13 | g.28018503A>C | CA16602448 | FLT3 | c.2505T>G (p.Asp835Glu) c.*417T>G (n.*417T>G) n.2719T>G c.2448T>G (p.Asp816Glu) c.1980T>G (p.Asp660Glu) c.2289T>G (p.Asp763Glu) c.1626T>G (p.Asp542Glu) c.1608T>G (p.Asp536Glu) n.2703T>G | ClinVar dbSNP |