| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32326504del | CA16614099 | BRCA2 | c.522del (p.Gln175ArgfsTer10) c.153del (p.Gln52ArgfsTer10) n.393del c.*301del (n.*301del) n.720del n.522del | ClinVar dbSNP |
| 13 | g.32326504T= | CA3200933542 | BRCA2 | c.522T= (p.Arg174=) c.153T= (p.Arg51=) n.393T= c.*301T= (n.*301T=) n.720T= n.522T= | dbSNP dbSNP |