| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32336621C>T | CA16043337 | BRCA2 | c.2266C>T (p.Gln756Ter) c.1897C>T (p.Gln633Ter) n.2266C>T | ClinVar dbSNP |
| 13 | g.32336621C>G | CA387771044 | BRCA2 | c.2266C>G (p.Gln756Glu) c.1897C>G (p.Gln633Glu) n.2266C>G | ClinVar dbSNP |
| 13 | g.32336621C>A | CA387771048 | BRCA2 | c.2266C>A (p.Gln756Lys) c.1897C>A (p.Gln633Lys) n.2266C>A | dbSNP |