| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32331015_32331016del | CA025258 | BRCA2 | c.778_779del (p.Glu260SerfsTer15) c.409_410del (p.Glu137SerfsTer15) c.*557_*558del (n.*557_*558del) n.976_977del n.778_779del | ClinVar dbSNP |
| 13 | g.32331013_32331016del | CA2622599904 | BRCA2 | c.776_779del (p.Arg259LysfsTer17) c.407_410del (p.Arg136LysfsTer17) c.*555_*558del (n.*555_*558del) n.974_977del n.776_779del | dbSNP gnomAD v4 |