Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32355232dup | CA913188635 | BRCA2 | c.7379dup (p.Asn2460LysfsTer15) c.7010dup (p.Asn2337LysfsTer15) n.7379dup c.7283dup (p.Asn2428LysfsTer15) | ClinVar dbSNP |
13 | g.32355232del | CA025050 | BRCA2 | c.7379del (p.Asn2460ThrfsTer7) c.7010del (p.Asn2337ThrfsTer7) n.7379del c.7379del (p.Asn2460ThrfsTer9) c.7283del (p.Asn2428ThrfsTer7) | ClinVar dbSNP |