| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28034183A>G | CA16603126 | FLT3 | c.1736T>C (p.Val579Ala) n.1818T>C c.1679T>C (p.Val560Ala) c.1211T>C (p.Val404Ala) c.1520T>C (p.Val507Ala) c.857T>C (p.Val286Ala) c.839T>C (p.Val280Ala) n.1802T>C | ClinVar dbSNP gnomAD v2 COSMIC |
| 13 | g.28034183A>C | CA387640999 | FLT3 | c.1736T>G (p.Val579Gly) n.1818T>G c.1679T>G (p.Val560Gly) c.1211T>G (p.Val404Gly) c.1520T>G (p.Val507Gly) c.857T>G (p.Val286Gly) c.839T>G (p.Val280Gly) n.1802T>G | dbSNP |