single nucleotide variant | NM_007294.4(BRCA1):c.5332G>A (p.Asp1778Asn) | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41203080 | 41203080 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA003491 |
single nucleotide variant | NM_007294.4(BRCA1):c.5333-1G>A | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41201212 | 41201212 | C | T | criteria provided, multiple submitters, no conflicts | ClinGen:CA003494 |
single nucleotide variant | NM_007294.4(BRCA1):c.5333-1G>C | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41201212 | 41201212 | C | G | criteria provided, multiple submitters, no conflicts | Breast Cancer Information Core (BIC) (BRCA1):5452-1&base_change=G to C,ClinGen:CA003496 |
single nucleotide variant | NM_007294.4(BRCA1):c.5333-2A>C | BRCA1 | Pathogenic | 17 | 41201213 | 41201213 | T | G | criteria provided, single submitter | ClinGen:CA003497 |
single nucleotide variant | NM_007294.4(BRCA1):c.5333-2A>T | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41201213 | 41201213 | T | A | criteria provided, multiple submitters, no conflicts | ClinGen:CA003498 |
single nucleotide variant | NM_007294.4(BRCA1):c.5333-3T>G | BRCA1 | Pathogenic | 17 | 41201214 | 41201214 | A | C | criteria provided, single submitter | ClinGen:CA003499 |
single nucleotide variant | NM_007294.4(BRCA1):c.5335C>T (p.Gln1779Ter) | BRCA1 | Pathogenic | 17 | 41201209 | 41201209 | G | A | reviewed by expert panel | ClinGen:CA003506 |
single nucleotide variant | NM_007294.4(BRCA1):c.5339T>C (p.Leu1780Pro) | BRCA1 | Pathogenic/Likely pathogenic | 17 | 41201205 | 41201205 | A | G | criteria provided, multiple submitters, no conflicts | ClinGen:CA003508 |
single nucleotide variant | NM_007294.4(BRCA1):c.5341G>T (p.Glu1781Ter) | BRCA1 | Pathogenic | 17 | 41201203 | 41201203 | C | A | reviewed by expert panel | ClinGen:CA003511 |
Deletion | NM_007294.4(BRCA1):c.5341del (p.Glu1781fs) | BRCA1 | Pathogenic | 17 | 41201203 | 41201203 | TC | T | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):5460&base_change=del G,ClinGen:CA003510 |