| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32340144T>C | CA387787167 | BRCA2 | c.5789T>C (p.Leu1930Ser) c.5420T>C (p.Leu1807Ser) n.5789T>C | ClinVar dbSNP |
| 13 | g.32340144T>G | CA387787169 | BRCA2 | c.5789T>G (p.Leu1930Ter) c.5420T>G (p.Leu1807Ter) n.5789T>G | ClinVar dbSNP |
| 13 | g.32340144T>A | CA023238 | BRCA2 | c.5789T>A (p.Leu1930Ter) c.5420T>A (p.Leu1807Ter) n.5789T>A | ClinVar dbSNP |