Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32333291del | CA013362 | BRCA2 | c.1813del (p.Ile605TyrfsTer9) c.1444del (p.Ile482TyrfsTer9) n.2011del n.1813del | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
13 | g.32333291dup | CA013353 | BRCA2 | c.1813dup (p.Ile605AsnfsTer11) c.1444dup (p.Ile482AsnfsTer11) n.1813dup | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |