| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32325169del | CA019541 | BRCA2 | c.410del (p.Ser137PhefsTer15) c.41del (p.Ser14PhefsTer15) n.281del c.*189del (n.*189del) n.608del n.410del | ClinVar dbSNP |
| 13 | g.32325169C= | CA2082747717 | BRCA2 | c.410C= (p.Ser137=) c.41C= (p.Ser14=) n.281C= c.*189C= (n.*189C=) n.608C= n.410C= | dbSNP dbSNP |