single nucleotide variant | NM_007294.4(BRCA1):c.121C>T (p.His41Tyr) | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41267756 | 41267756 | G | A | criteria provided, multiple submitters, no conflicts | - |
Duplication | NM_000059.4(BRCA2):c.6155dup (p.Ser2053fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32914646 | 32914647 | T | TC | criteria provided, multiple submitters, no conflicts | - |
Indel | NM_000059.3(BRCA2):c.5362_5363delinsA (p.Ser1788fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32913854 | 32913855 | TC | A | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000059.4(BRCA2):c.1774del (p.Tyr592fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32907387 | 32907387 | AT | A | criteria provided, multiple submitters, no conflicts | - |
Duplication | NM_000059.4(BRCA2):c.610dup (p.Leu204fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32900726 | 32900727 | A | AC | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000059.4(BRCA2):c.8954-2_8959del | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32953883 | 32953890 | AACAGTTAT | A | criteria provided, multiple submitters, no conflicts | - |
Duplication | NM_000059.4(BRCA2):c.7958_7959dup (p.Leu2654fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32936811 | 32936812 | C | CTT | criteria provided, multiple submitters, no conflicts | - |
single nucleotide variant | NM_000059.4(BRCA2):c.6859A>T (p.Arg2287Ter) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32918712 | 32918712 | A | T | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_000059.4(BRCA2):c.9593_9594del (p.Cys3198fs) | BRCA2 | Pathogenic/Likely pathogenic | 13 | 32971125 | 32971126 | CTG | C | criteria provided, multiple submitters, no conflicts | - |
Deletion | NM_007294.4(BRCA1):c.4810del (p.Gln1604fs) | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41223121 | 41223121 | TG | T | criteria provided, multiple submitters, no conflicts | - |