Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32354921dup | CA658823681 | BRCA2 | c.7068dup (p.Leu2357SerfsTer3) c.6699dup (p.Leu2234SerfsTer3) n.7068dup c.6972dup (p.Leu2325SerfsTer3) | ClinVar dbSNP |
13 | g.32354920_32354921del | CA024828 | BRCA2 | c.7067_7068del (p.Phe2356SerfsTer3) c.6698_6699del (p.Phe2233SerfsTer3) n.7067_7068del c.6971_6972del (p.Phe2324SerfsTer3) | ClinVar dbSNP |