| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32338313G>C | CA387778909 | BRCA2 | c.3958G>C (p.Glu1320Gln) c.3589G>C (p.Glu1197Gln) n.3958G>C | dbSNP |
| 13 | g.32338313G>A | CA10583097 | BRCA2 | c.3958G>A (p.Glu1320Lys) c.3589G>A (p.Glu1197Lys) n.3958G>A | ClinVar dbSNP |
| 13 | g.32338313G>T | CA019267 | BRCA2 | c.3958G>T (p.Glu1320Ter) c.3589G>T (p.Glu1197Ter) n.3958G>T | ClinVar dbSNP |