| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28027222A>C | CA16602564 | FLT3 | c.2073T>G (p.Phe691Leu) n.2155T>G c.2016T>G (p.Phe672Leu) c.1548T>G (p.Phe516Leu) c.1857T>G (p.Phe619Leu) c.1194T>G (p.Phe398Leu) c.1176T>G (p.Phe392Leu) n.2139T>G | ClinVar dbSNP gnomAD v4 COSMIC |
| 13 | g.28027222A>T | CA16602565 | FLT3 | c.2073T>A (p.Phe691Leu) n.2155T>A c.2016T>A (p.Phe672Leu) c.1548T>A (p.Phe516Leu) c.1857T>A (p.Phe619Leu) c.1194T>A (p.Phe398Leu) c.1176T>A (p.Phe392Leu) n.2139T>A | ClinVar dbSNP |
| 13 | g.28027222A= | CA2080790188 | FLT3 | c.2073T= (p.Phe691=) n.2155T= c.2016T= (p.Phe672=) c.1548T= (p.Phe516=) c.1857T= (p.Phe619=) c.1194T= (p.Phe398=) c.1176T= (p.Phe392=) n.2139T= | dbSNP |