Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.130873027T>C | CA16602581 | ABL1 | c.1132T>C (p.Phe378Leu) c.1075T>C (p.Phe359Leu) | ClinVar dbSNP |
9 | g.130873027T>G | CA16602557 | ABL1 | c.1132T>G (p.Phe378Val) c.1075T>G (p.Phe359Val) | ClinVar dbSNP COSMIC |
9 | g.130873027T>A | CA16602580 | ABL1 | c.1132T>A (p.Phe378Ile) c.1075T>A (p.Phe359Ile) | ClinVar dbSNP COSMIC |