| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 21 | g.34859530A>T | CA248819 | RUNX1 | c.557T>A (p.Val186Asp) c.476T>A (p.Val159Asp) c.521T>A (p.Val174Asp) n.49T>A c.*147T>A (n.*147T>A) c.518T>A (p.Val173Asp) n.736T>A c.404T>A (p.Val135Asp) n.783T>A | ClinVar dbSNP |
| 21 | g.34859530A>C | CA410208053 | RUNX1 | c.557T>G (p.Val186Gly) c.476T>G (p.Val159Gly) c.521T>G (p.Val174Gly) n.49T>G c.*147T>G (n.*147T>G) c.518T>G (p.Val173Gly) n.736T>G c.404T>G (p.Val135Gly) n.783T>G | ClinVar dbSNP |
| 21 | g.34859530A>G | CA410208054 | RUNX1 | c.557T>C (p.Val186Ala) c.476T>C (p.Val159Ala) c.521T>C (p.Val174Ala) n.49T>C c.*147T>C (n.*147T>C) c.518T>C (p.Val173Ala) n.736T>C c.404T>C (p.Val135Ala) n.783T>C | ClinVar dbSNP |