Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32338000_32338001delinsTAAAAAG | CA018463 | BRCA2 | c.3645_3646delinsTAAAAAG (p.Phe1216LysfsTer14) c.3276_3277delinsTAAAAAG (p.Phe1093LysfsTer14) n.3645_3646delinsTAAAAAG | ClinVar dbSNP |
13 | g.32338000_32338001dup | CA2573149329 | BRCA2 | c.3645_3646dup (p.Phe1216CysfsTer13) c.3276_3277dup (p.Phe1093CysfsTer13) n.3645_3646dup | ClinVar dbSNP |