| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.130872901T>A | CA16602577 | ABL1 | c.1006T>A (p.Phe336Ile) c.949T>A (p.Phe317Ile) | ClinVar dbSNP |
| 9 | g.130872901T>C | CA16602794 | ABL1 | c.1006T>C (p.Phe336Leu) c.949T>C (p.Phe317Leu) | ClinVar dbSNP COSMIC |
| 9 | g.130872901T>G | CA16602578 | ABL1 | c.1006T>G (p.Phe336Val) c.949T>G (p.Phe317Val) | ClinVar dbSNP COSMIC |