Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.130862969G>C | CA16602548 | ABL1 | c.813G>C (p.Gln271His) c.756G>C (p.Gln252His) | ClinVar dbSNP COSMIC |
9 | g.130862969G>A | CA467496369 | ABL1 | c.813G>A (p.Gln271=) c.756G>A (p.Gln252=) | dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
9 | g.130862969G>T | CA16602549 | ABL1 | c.813G>T (p.Gln271His) c.756G>T (p.Gln252His) | ClinVar dbSNP COSMIC |