Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.130862976G>A | CA16602551 | ABL1 | c.820G>A (p.Glu274Lys) c.763G>A (p.Glu255Lys) | ClinVar dbSNP gnomAD v4 COSMIC |
9 | g.130862976G= | CA1881463513 | ABL1 | c.820G= (p.Glu274=) c.763G= (p.Glu255=) | dbSNP |
9 | g.130862976G>C | CA375263317 | ABL1 | c.820G>C (p.Glu274Gln) c.763G>C (p.Glu255Gln) | dbSNP gnomAD v4 |