Deletion | NM_024675.4(PALB2):c.76del (p.Arg26fs) | PALB2 | Pathogenic/Likely pathogenic | 16 | 23649423 | 23649423 | CT | C | 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 | - |
single nucleotide variant | NM_024675.4(PALB2):c.211+1G>T | PALB2 | Pathogenic/Likely pathogenic | 16 | 23649170 | 23649170 | C | A | criteria provided, multiple submitters, no conflicts | - |