single nucleotide variant | NM_000059.4(BRCA2):c.6800C>A (p.Ser2267Ter) | BRCA2 | Pathogenic | 13 | 32915292 | 32915292 | C | A | reviewed by expert panel | ClinGen:CA024416 |
Deletion | NM_000059.4(BRCA2):c.6809del (p.Gly2270fs) | BRCA2 | Pathogenic | 13 | 32915300 | 32915300 | TG | T | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):7037&base_change=del G,ClinGen:CA024424 |
single nucleotide variant | NM_000059.4(BRCA2):c.681+4A>G | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32903633 | 32903633 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA024432 |
Deletion | NM_000059.4(BRCA2):c.6814del (p.Arg2272fs) | BRCA2 | Pathogenic | 13 | 32915302 | 32915302 | GA | G | reviewed by expert panel | ClinGen:CA024434 |
Deletion | NM_000059.4(BRCA2):c.6816_6817del (p.Gly2274fs) | BRCA2 | Pathogenic | 13 | 32915308 | 32915309 | GAA | G | reviewed by expert panel | ClinGen:CA024440 |
single nucleotide variant | NM_000059.4(BRCA2):c.682-1G>C | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32905055 | 32905055 | G | C | criteria provided, multiple submitters, no conflicts | Breast Cancer Information Core (BIC) (BRCA2):910-1&base_change=G to C,ClinGen:CA024456 |
Deletion | NM_000059.4(BRCA2):c.6833_6837del (p.Ile2278fs) | BRCA2 | Pathogenic | 13 | 32915321 | 32915325 | CCTTAT | C | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):7057&base_change=del CTTAT,Breast Cancer Information Core (BIC) (BRCA2):7061&base_change=del TCTTA,ClinGen:CA024468 |
Deletion | NM_000059.4(BRCA2):c.6841+1del | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32915332 | 32915332 | TG | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA024488 |
single nucleotide variant | NM_000059.4(BRCA2):c.6938-2A>G | BRCA2 | Pathogenic | 13 | 32920962 | 32920962 | A | G | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA2):7166-2&base_change=A to G,ClinGen:CA024592 |
Deletion | NM_000059.4(BRCA2):c.6959del (p.Leu2320fs) | BRCA2 | Pathogenic | 13 | 32920984 | 32920984 | AT | A | reviewed by expert panel | ClinGen:CA024633 |