| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32339214T>G | CA020929 | BRCA2 | c.4859T>G (p.Leu1620Ter) c.4490T>G (p.Leu1497Ter) n.4859T>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.32339214T>A | CA387783418 | BRCA2 | c.4859T>A (p.Leu1620Ter) c.4490T>A (p.Leu1497Ter) n.4859T>A | dbSNP |
| 13 | g.32339214T= | CA2082816448 | BRCA2 | c.4859T= (p.Leu1620=) c.4490T= (p.Leu1497=) n.4859T= | dbSNP |
| 13 | g.32339214T>C | CA387783420 | BRCA2 | c.4859T>C (p.Leu1620Ser) c.4490T>C (p.Leu1497Ser) n.4859T>C | dbSNP gnomAD v4 |