| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.32357862C>T | CA025250 | BRCA2 | c.7738C>T (p.Gln2580Ter) c.7369C>T (p.Gln2457Ter) c.205C>T (p.Gln69Ter) c.303C>T n.7738C>T c.7642C>T (p.Gln2548Ter) | ClinVar dbSNP |
| 13 | g.32357862C>A | CA387745610 | BRCA2 | c.7738C>A (p.Gln2580Lys) c.7369C>A (p.Gln2457Lys) c.205C>A (p.Gln69Lys) c.303C>A n.7738C>A c.7642C>A (p.Gln2548Lys) | ClinVar dbSNP COSMIC COSMIC |
| 13 | g.32357862C= | CA2082818595 | BRCA2 | c.7738C= (p.Gln2580=) c.7369C= (p.Gln2457=) c.205C= (p.Gln69=) c.303C= n.7738C= c.7642C= (p.Gln2548=) | dbSNP |