Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32357778del | CA891842180 | BRCA2 | c.7654del (p.Ile2552LeufsTer?) c.7285del (p.Ile2429LeufsTer?) c.121del (p.Ile41LeufsTer?) c.219del n.7654del c.7558del (p.Ile2520LeufsTer?) | ClinVar dbSNP gnomAD v4 |
13 | g.32357778dup | CA10586078 | BRCA2 | c.7654dup (p.Ile2552AsnfsTer2) c.7285dup (p.Ile2429AsnfsTer2) c.121dup (p.Ile41AsnfsTer2) c.219dup n.7654dup c.7558dup (p.Ile2520AsnfsTer2) | ClinVar dbSNP |