| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28034204T>A | CA387641123 | FLT3 | c.1715A>T (p.Tyr572Phe) n.1797A>T c.1658A>T (p.Tyr553Phe) c.1190A>T (p.Tyr397Phe) c.1499A>T (p.Tyr500Phe) c.836A>T (p.Tyr279Phe) c.818A>T (p.Tyr273Phe) n.1781A>T | dbSNP |
| 13 | g.28034204T>C | CA6928567 | FLT3 | c.1715A>G (p.Tyr572Cys) n.1797A>G c.1658A>G (p.Tyr553Cys) c.1190A>G (p.Tyr397Cys) c.1499A>G (p.Tyr500Cys) c.836A>G (p.Tyr279Cys) c.818A>G (p.Tyr273Cys) n.1781A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |