| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28018484A>T | CA387650162 | FLT3 | c.2524T>A (p.Tyr842Asn) c.*436T>A (n.*436T>A) n.2738T>A c.2467T>A (p.Tyr823Asn) c.1999T>A (p.Tyr667Asn) c.2308T>A (p.Tyr770Asn) c.1645T>A (p.Tyr549Asn) c.1627T>A (p.Tyr543Asn) n.2722T>A | dbSNP |
| 13 | g.28018484A>G | CA16602562 | FLT3 | c.2524T>C (p.Tyr842His) c.*436T>C (n.*436T>C) n.2738T>C c.2467T>C (p.Tyr823His) c.1999T>C (p.Tyr667His) c.2308T>C (p.Tyr770His) c.1645T>C (p.Tyr549His) c.1627T>C (p.Tyr543His) n.2722T>C | ClinVar dbSNP COSMIC |
| 13 | g.28018484A= | CA2080781370 | FLT3 | c.2524T= (p.Tyr842=) c.*436T= (n.*436T=) n.2738T= c.2467T= (p.Tyr823=) c.1999T= (p.Tyr667=) c.2308T= (p.Tyr770=) c.1645T= (p.Tyr549=) c.1627T= (p.Tyr543=) n.2722T= | dbSNP |