| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32337751A>G | CA017926 | BRCA2 | c.3396A>G (p.Lys1132=) c.3027A>G (p.Lys1009=) n.3396A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.32337751A>C | CA017920 | BRCA2 | c.3396A>C (p.Lys1132Asn) c.3027A>C (p.Lys1009Asn) n.3396A>C | ClinVar dbSNP |
| 13 | g.32337751A= | CA1630855867 | BRCA2 | c.3396A= (p.Lys1132=) c.3027A= (p.Lys1009=) n.3396A= | dbSNP |