| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28018504T>G | CA16602450 | FLT3 | c.2504A>C (p.Asp835Ala) c.*416A>C (n.*416A>C) n.2718A>C c.2447A>C (p.Asp816Ala) c.1979A>C (p.Asp660Ala) c.2288A>C (p.Asp763Ala) c.1625A>C (p.Asp542Ala) c.1607A>C (p.Asp536Ala) n.2702A>C | ClinVar dbSNP COSMIC |
| 13 | g.28018504T>A | CA126344 | FLT3 | c.2504A>T (p.Asp835Val) c.*416A>T (n.*416A>T) n.2718A>T c.2447A>T (p.Asp816Val) c.1979A>T (p.Asp660Val) c.2288A>T (p.Asp763Val) c.1625A>T (p.Asp542Val) c.1607A>T (p.Asp536Val) n.2702A>T | ClinVar dbSNP COSMIC |
| 13 | g.28018504T>C | CA387650200 | FLT3 | c.2504A>G (p.Asp835Gly) c.*416A>G (n.*416A>G) n.2718A>G c.2447A>G (p.Asp816Gly) c.1979A>G (p.Asp660Gly) c.2288A>G (p.Asp763Gly) c.1625A>G (p.Asp542Gly) c.1607A>G (p.Asp536Gly) n.2702A>G | dbSNP |