Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.130872903C>T | CA467395081 | ABL1 | c.1008C>T (p.Phe336=) c.951C>T (p.Phe317=) | dbSNP gnomAD v4 |
9 | g.130872903C>G | CA16602555 | ABL1 | c.1008C>G (p.Phe336Leu) c.951C>G (p.Phe317Leu) | ClinVar dbSNP COSMIC |
9 | g.130872903C>A | CA16602554 | ABL1 | c.1008C>A (p.Phe336Leu) c.951C>A (p.Phe317Leu) | ClinVar dbSNP COSMIC |