| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28018505C>G | CA280208 | FLT3 | c.2503G>C (p.Asp835His) c.*415G>C (n.*415G>C) n.2717G>C c.2446G>C (p.Asp816His) c.1978G>C (p.Asp660His) c.2287G>C (p.Asp763His) c.1624G>C (p.Asp542His) c.1606G>C (p.Asp536His) n.2701G>C | ClinVar dbSNP COSMIC |
| 13 | g.28018505C>T | CA280211 | FLT3 | c.2503G>A (p.Asp835Asn) c.*415G>A (n.*415G>A) n.2717G>A c.2446G>A (p.Asp816Asn) c.1978G>A (p.Asp660Asn) c.2287G>A (p.Asp763Asn) c.1624G>A (p.Asp542Asn) c.1606G>A (p.Asp536Asn) n.2701G>A | ClinVar dbSNP COSMIC |
| 13 | g.28018505C>A | CA126347 | FLT3 | c.2503G>T (p.Asp835Tyr) c.*415G>T (n.*415G>T) n.2717G>T c.2446G>T (p.Asp816Tyr) c.1978G>T (p.Asp660Tyr) c.2287G>T (p.Asp763Tyr) c.1624G>T (p.Asp542Tyr) c.1606G>T (p.Asp536Tyr) n.2701G>T | ClinVar dbSNP COSMIC |