Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32340075_32340078del | CA023043 | BRCA2 | c.5720_5723del (p.Ser1907Ter) c.5351_5354del (p.Ser1784Ter) n.5720_5723del | ClinVar dbSNP |
13 | g.32340077_32340078del | CA023040 | BRCA2 | c.5722_5723del (p.Leu1908ArgfsTer2) c.5353_5354del (p.Leu1785ArgfsTer2) n.5722_5723del | ClinVar dbSNP gnomAD v2 gnomAD v4 |