| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32336849G>T | CA015478 | BRCA2 | c.2494G>T (p.Glu832Ter) c.2125G>T (p.Glu709Ter) n.2494G>T | ClinVar dbSNP |
| 13 | g.32336849G>C | CA387772411 | BRCA2 | c.2494G>C (p.Glu832Gln) c.2125G>C (p.Glu709Gln) n.2494G>C | ClinVar dbSNP |
| 13 | g.32336849G>A | CA387772410 | BRCA2 | c.2494G>A (p.Glu832Lys) c.2125G>A (p.Glu709Lys) n.2494G>A | dbSNP COSMIC COSMIC |