Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.32338179_32338182del | CA018874 | BRCA2 | c.3824_3827del (p.Ile1275LysfsTer8) c.3455_3458del (p.Ile1152LysfsTer8) n.3824_3827del | ClinVar dbSNP |
13 | g.32338179_32338182dup | CA2499222146 | BRCA2 | c.3824_3827dup (p.Glu1276AspfsTer5) c.3455_3458dup (p.Glu1153AspfsTer5) n.3824_3827dup | ClinVar dbSNP |