| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28028279T>A | CA387652299 | FLT3 | c.1952A>T (p.Asp651Val) n.2034A>T c.1895A>T (p.Asp632Val) c.1427A>T (p.Asp476Val) c.1736A>T (p.Asp579Val) c.1073A>T (p.Asp358Val) c.1055A>T (p.Asp352Val) n.2018A>T | dbSNP |
| 13 | g.28028279T>G | CA387652298 | FLT3 | c.1952A>C (p.Asp651Ala) n.2034A>C c.1895A>C (p.Asp632Ala) c.1427A>C (p.Asp476Ala) c.1736A>C (p.Asp579Ala) c.1073A>C (p.Asp358Ala) c.1055A>C (p.Asp352Ala) n.2018A>C | dbSNP |
| 13 | g.28028279T>C | CA16602570 | FLT3 | c.1952A>G (p.Asp651Gly) n.2034A>G c.1895A>G (p.Asp632Gly) c.1427A>G (p.Asp476Gly) c.1736A>G (p.Asp579Gly) c.1073A>G (p.Asp358Gly) c.1055A>G (p.Asp352Gly) n.2018A>G | ClinVar dbSNP gnomAD v4 |