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 |