| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.28034144A>G | CA16603130 | FLT3 | c.1775T>C (p.Val592Ala) n.1857T>C c.1718T>C (p.Val573Ala) c.1250T>C (p.Val417Ala) c.1559T>C (p.Val520Ala) c.896T>C (p.Val299Ala) c.878T>C (p.Val293Ala) n.1841T>C | ClinVar dbSNP gnomAD v4 COSMIC |
| 13 | g.28034144A>T | CA387640795 | FLT3 | c.1775T>A (p.Val592Asp) n.1857T>A c.1718T>A (p.Val573Asp) c.1250T>A (p.Val417Asp) c.1559T>A (p.Val520Asp) c.896T>A (p.Val299Asp) c.878T>A (p.Val293Asp) n.1841T>A | dbSNP COSMIC |
| 13 | g.28034144A>C | CA387640792 | FLT3 | c.1775T>G (p.Val592Gly) n.1857T>G c.1718T>G (p.Val573Gly) c.1250T>G (p.Val417Gly) c.1559T>G (p.Val520Gly) c.896T>G (p.Val299Gly) c.878T>G (p.Val293Gly) n.1841T>G | dbSNP COSMIC |