Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32338639dup | CA019907 | BRCA2 | c.4284dup (p.Gln1429SerfsTer9) c.3915dup (p.Gln1306SerfsTer9) n.4284dup | ClinVar dbSNP gnomAD v2 gnomAD v4 |
13 | g.32338639del | CA658823573 | BRCA2 | c.4284del (p.Gln1429ArgfsTer19) c.3915del (p.Gln1306ArgfsTer19) n.4284del | ClinVar dbSNP gnomAD v4 |