Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32340206_32340209del | CA023297 | BRCA2 | c.5851_5854del (p.Ser1951TrpfsTer11) c.5482_5485del (p.Ser1828TrpfsTer11) n.5851_5854del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
13 | g.32340206_32340209dup | CA023304 | BRCA2 | c.5851_5854dup (p.Leu1952Ter) c.5482_5485dup (p.Leu1829Ter) n.5851_5854dup | ClinVar dbSNP |