| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.130862955C>G | CA16602546 | ABL1 | c.799C>G (p.Leu267Val) c.742C>G (p.Leu248Val) | ClinVar dbSNP COSMIC |
| 9 | g.130862955C>A | CA375263219 | ABL1 | c.799C>A (p.Leu267Met) c.742C>A (p.Leu248Met) | dbSNP |
| 9 | g.130862955C= | CA1881463407 | ABL1 | c.799C= (p.Leu267=) c.742C= (p.Leu248=) | dbSNP |