Deletion | NM_007294.4(BRCA1):c.2295del (p.Ser766fs) | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41245253 | 41245253 | TC | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000059.4(BRCA2):c.3600T>A (p.Cys1200Ter) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32912092 | 32912092 | T | A | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000059.4(BRCA2):c.8941_8944del (p.Glu2981fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32953637 | 32953640 | AAAAG | A | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000059.4(BRCA2):c.9672del (p.Tyr3225fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32972322 | 32972322 | TA | T | criteria provided, multiple submitters, no conflicts | - |
Insertion | NM_007294.4(BRCA1):c.1641_1642insG (p.Ile548fs) | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41245906 | 41245907 | T | TC | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_007294.4(BRCA1):c.139T>C (p.Cys47Arg) | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41258546 | 41258546 | A | G | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_007294.4(BRCA1):c.70T>G (p.Cys24Gly) | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41276044 | 41276044 | A | C | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000059.4(BRCA2):c.7976+1G>T | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32936831 | 32936831 | G | T | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000059.4(BRCA2):c.7007+2T>G | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32921035 | 32921035 | T | G | criteria provided, multiple submitters, no conflicts | - |