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.1513A>T (p.Lys505Ter) | BRCA1 | Pathogenic | 17 | 41246035 | 41246035 | T | A | reviewed by expert panel | ClinGen:CA001022 |
Insertion | NM_007294.4(BRCA1):c.1513_1514insT (p.Lys505fs) | BRCA1 | Pathogenic | 17 | 41246034 | 41246035 | T | TA | reviewed by expert panel | ClinGen:CA001021 |
Deletion | NM_007294.4(BRCA1):c.1517_1521del (p.Arg506fs) | BRCA1 | Pathogenic | 17 | 41246027 | 41246031 | GTCTCC | G | reviewed by expert panel | ClinGen:CA001023 |
single nucleotide variant | NM_007294.4(BRCA1):c.1519A>T (p.Arg507Ter) | BRCA1 | Pathogenic | 17 | 41246029 | 41246029 | T | A | reviewed by expert panel | ClinGen:CA001026 |
Deletion | NM_007294.4(BRCA1):c.1523del (p.Pro508fs) | BRCA1 | Pathogenic | 17 | 41246025 | 41246025 | AG | A | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):1642&base_change=del C,ClinGen:CA001029 |
single nucleotide variant | NM_007294.4(BRCA1):c.1529C>G (p.Ser510Ter) | BRCA1 | Pathogenic | 17 | 41246019 | 41246019 | G | C | reviewed by expert panel | ClinGen:CA001030 |
Deletion | NM_007294.4(BRCA1):c.1530del (p.Gly511fs) | BRCA1 | Pathogenic | 17 | 41246018 | 41246018 | CT | C | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):1649&base_change=del A,ClinGen:CA001031 |
Deletion | NM_007294.4(BRCA1):c.1551del (p.Phe517fs) | BRCA1 | Pathogenic | 17 | 41245997 | 41245997 | TA | T | reviewed by expert panel | Breast Cancer Information Core (BIC) (BRCA1):1670&base_change=del T,ClinGen:CA001040 |
Indel | NM_007294.4(BRCA1):c.1561_1564delinsTAAA (p.Ala521_Asp522delinsTer) | BRCA1 | Pathogenic | 17 | 41245984 | 41245987 | CTGC | TTTA | reviewed by expert panel | ClinGen:CA001045 |
Deletion | NM_007294.4(BRCA1):c.1570del (p.Ala524fs) | BRCA1 | Pathogenic | 17 | 41245978 | 41245978 | GC | G | reviewed by expert panel | ClinGen:CA001051 |