| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32337398A>T | CA017082 | BRCA2 | c.3043A>T (p.Lys1015Ter) c.2674A>T (p.Lys892Ter) n.3043A>T | ClinVar dbSNP |
| 13 | g.32337398A>C | CA387775011 | BRCA2 | c.3043A>C (p.Lys1015Gln) c.2674A>C (p.Lys892Gln) n.3043A>C | ClinVar dbSNP |
| 13 | g.32337398A>G | CA387775006 | BRCA2 | c.3043A>G (p.Lys1015Glu) c.2674A>G (p.Lys892Glu) n.3043A>G | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32337398A= | CA2082813817 | BRCA2 | c.3043A= (p.Lys1015=) c.2674A= (p.Lys892=) n.3043A= | dbSNP |