Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.43063374del | CA003308 | BRCA1 | c.5152del c.5155del c.5029del c.5149del c.5077del c.1843del c.1705del c.4267del c.5032del c.5221del c.5014del c.1717del c.5218del c.1542del c.1729del c.*4938del c.1468del c.85del c.628del c.-98-13181del (n.-98-13181del) n.5291del n.5332del | ClinVar dbSNP |
17 | g.43063374dup | CA10589615 | BRCA1 | c.5152dup c.5155dup c.5029dup c.5149dup c.5077dup c.1843dup c.1705dup c.4267dup c.5032dup c.5221dup c.5014dup c.1717dup c.5218dup c.1542dup c.1729dup c.*4938dup c.1468dup c.85dup c.628dup c.-98-13181dup (n.-98-13181dup) n.5291dup n.5332dup | ClinVar dbSNP |