| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32340912C>G | CA10589391 | BRCA2 | c.6557C>G (p.Ser2186Ter) c.6188C>G (p.Ser2063Ter) n.6557C>G | ClinVar dbSNP |
| 13 | g.32340912C>A | CA024166 | BRCA2 | c.6557C>A (p.Ser2186Ter) c.6188C>A (p.Ser2063Ter) n.6557C>A | ClinVar dbSNP |
| 13 | g.32340912C>T | CA16614339 | BRCA2 | c.6557C>T (p.Ser2186Leu) c.6188C>T (p.Ser2063Leu) n.6557C>T | ClinVar dbSNP |