Indel | NM_007294.4(BRCA1):c.2589_2594delinsATTCTTTT (p.Ser864fs) | BRCA1 | Pathogenic | 17 | 41244954 | 41244959 | TTTGAA | AAAAGAAT | criteria provided, single submitter | - |
Indel | NM_007294.4(BRCA1):c.2143_2155delinsTCTTT (p.Thr715fs) | BRCA1 | Pathogenic | 17 | 41245393 | 41245405 | TAAGTTCACTGGT | AAAGA | criteria provided, multiple submitters, no conflicts | - |
Duplication | NM_007294.4(BRCA1):c.2066dup (p.Ser689fs) | BRCA1 | Pathogenic | 17 | 41245481 | 41245482 | A | AC | criteria provided, single submitter | - |
Deletion | NM_007294.4(BRCA1):c.1785del (p.Glu595fs) | BRCA1 | Pathogenic | 17 | 41245763 | 41245763 | GT | G | criteria provided, single submitter | - |
Deletion | NM_007294.4(BRCA1):c.954del (p.His318fs) | BRCA1 | Pathogenic | 17 | 41246594 | 41246594 | TA | T | criteria provided, single submitter | - |
single nucleotide variant | NM_007294.4(BRCA1):c.520C>T (p.Gln174Ter) | BRCA1 | Pathogenic | 17 | 41251819 | 41251819 | G | A | criteria provided, single submitter | - |
single nucleotide variant | NM_007294.4(BRCA1):c.4485-2A>C | BRCA1 | Likely pathogenic | 17 | 41226540 | 41226540 | T | G | criteria provided, multiple submitters, no conflicts | - |
Duplication | NM_007294.4(BRCA1):c.4382_4388dup (p.Tyr1463Ter) | BRCA1 | Pathogenic | 17 | 41228600 | 41228601 | G | GTATTCAC | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_007294.4(BRCA1):c.3033_3034del (p.Glu1013fs) | BRCA1 | Pathogenic | 17 | 41244514 | 41244515 | CTT | C | criteria provided, multiple submitters, no conflicts | - |
Deletion | NC_000013.11:g.(?_32315480)_(32316547_?)del | BRCA2 | Pathogenic | 13 | 32889617 | 32890684 | na | na | criteria provided, single submitter | - |