| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28034139A>T | CA387640767 | FLT3 | c.1780T>A (p.Phe594Ile) n.1862T>A c.1723T>A (p.Phe575Ile) c.1255T>A (p.Phe419Ile) c.1564T>A (p.Phe522Ile) c.901T>A (p.Phe301Ile) c.883T>A (p.Phe295Ile) n.1846T>A | dbSNP COSMIC |
| 13 | g.28034139A>C | CA387640763 | FLT3 | c.1780T>G (p.Phe594Val) n.1862T>G c.1723T>G (p.Phe575Val) c.1255T>G (p.Phe419Val) c.1564T>G (p.Phe522Val) c.901T>G (p.Phe301Val) c.883T>G (p.Phe295Val) n.1846T>G | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 13 | g.28034139A>G | CA16603125 | FLT3 | c.1780T>C (p.Phe594Leu) n.1862T>C c.1723T>C (p.Phe575Leu) c.1255T>C (p.Phe419Leu) c.1564T>C (p.Phe522Leu) c.901T>C (p.Phe301Leu) c.883T>C (p.Phe295Leu) n.1846T>C | ClinVar dbSNP COSMIC |