| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32357795del | CA025216 | BRCA2 | c.7671del (p.Glu2558SerfsTer?) c.7302del (p.Glu2435SerfsTer?) c.138del (p.Glu47SerfsTer?) c.236del n.7671del c.7575del (p.Glu2526SerfsTer?) | ClinVar dbSNP |
| 13 | g.32357795A= | CA2082818045 | BRCA2 | c.7671A= (p.Ala2557=) c.7302A= (p.Ala2434=) c.138A= (p.Ala46=) c.236A= n.7671A= c.7575A= (p.Ala2525=) | dbSNP dbSNP |