| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32356521T>C | CA025134 | BRCA2 | c.7529T>C (p.Leu2510Pro) c.7160T>C (p.Leu2387Pro) c.94T>C n.7529T>C c.7433T>C (p.Leu2478Pro) | ClinVar dbSNP |
| 13 | g.32356521T>G | CA387743580 | BRCA2 | c.7529T>G (p.Leu2510Arg) c.7160T>G (p.Leu2387Arg) c.94T>G n.7529T>G c.7433T>G (p.Leu2478Arg) | ClinVar dbSNP |
| 13 | g.32356521T>A | CA387743582 | BRCA2 | c.7529T>A (p.Leu2510Gln) c.7160T>A (p.Leu2387Gln) c.94T>A n.7529T>A c.7433T>A (p.Leu2478Gln) | dbSNP |
| 13 | g.32356521T= | CA2082814862 | BRCA2 | c.7529T= (p.Leu2510=) c.7160T= (p.Leu2387=) c.94T= n.7529T= c.7433T= (p.Leu2478=) | dbSNP |