| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32339462G>A | CA387784131 | BRCA2 | c.5107G>A (p.Glu1703Lys) c.4738G>A (p.Glu1580Lys) n.5107G>A | dbSNP |
| 13 | g.32339462G>C | CA021267 | BRCA2 | c.5107G>C (p.Glu1703Gln) c.4738G>C (p.Glu1580Gln) n.5107G>C | ClinVar dbSNP |
| 13 | g.32339462G>T | CA021274 | BRCA2 | c.5107G>T (p.Glu1703Ter) c.4738G>T (p.Glu1580Ter) n.5107G>T | ClinVar dbSNP |