Type | Name | Gene Symbol | Clinical Significance | Chromosome | Start | Stop | Reference Allele | Alternate Allele | Review Status | Other IDs |
---|---|---|---|---|---|---|---|---|---|---|
(GRCh37) | ||||||||||
single nucleotide variant | NM_007294.4(BRCA1):c.1729G>T (p.Glu577Ter) | BRCA1 | Pathogenic | 17 | 41245819 | 41245819 | C | A | reviewed by expert panel | ClinGen:CA001133 |
Deletion | NM_007294.4(BRCA1):c.1729_1730del (p.Glu577fs) | BRCA1 | Pathogenic | 17 | 41245818 | 41245819 | TTC | T | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):1848&base_change=del GA,ClinGen:CA001132 |
single nucleotide variant | NM_007294.4(BRCA1):c.1741A>T (p.Lys581Ter) | BRCA1 | Pathogenic | 17 | 41245807 | 41245807 | T | A | reviewed by expert panel | ClinGen:CA001139 |
single nucleotide variant | NM_007294.4(BRCA1):c.1747A>T (p.Lys583Ter) | BRCA1 | Pathogenic | 17 | 41245801 | 41245801 | T | A | reviewed by expert panel | ClinGen:CA001145 |
Deletion | NM_007294.4(BRCA1):c.1757del (p.Pro586fs) | BRCA1 | Pathogenic | 17 | 41245791 | 41245791 | AG | A | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):1876&base_change=del C,ClinGen:CA001148 |
Deletion | NM_007294.4(BRCA1):c.1772del (p.Ile591fs) | BRCA1 | Pathogenic | 17 | 41245776 | 41245776 | TA | T | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):1891&base_change=del T,ClinGen:CA001152 |
single nucleotide variant | NM_007294.4(BRCA1):c.1789G>T (p.Glu597Ter) | BRCA1 | Pathogenic | 17 | 41245759 | 41245759 | C | A | reviewed by expert panel | ClinGen:CA001161 |
single nucleotide variant | NM_007294.4(BRCA1):c.178C>T (p.Gln60Ter) | BRCA1 | Pathogenic | 17 | 41258507 | 41258507 | G | A | reviewed by expert panel | ClinGen:CA001162 |
single nucleotide variant | NM_007294.4(BRCA1):c.1793T>A (p.Leu598Ter) | BRCA1 | Pathogenic | 17 | 41245755 | 41245755 | A | T | reviewed by expert panel | ClinGen:CA001163 |
single nucleotide variant | NM_007294.4(BRCA1):c.1793T>G (p.Leu598Ter) | BRCA1 | Pathogenic | 17 | 41245755 | 41245755 | A | C | reviewed by expert panel | ClinGen:CA001164 |