Variant · Snv
BRCA1 C61G
CI-VAR-00000337Explore in graph →NP_009225.1:p.Cys61GlyNM_007294.3:c.181T>GClinVar 17661 CIViC 1238 rs28897672
Curated evidence
Evidence by cancer (0 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 17661 | Pathogenic | reviewed by expert panel | 3 | Breast-ovarian cancer, familial, susceptibility to, 1; Hereditary breast ovarian cancer syndrome; Hereditary cancer-predisposing syndrome; Familial cancer of breast; Breast carcinoma; Breast neoplasm; Ovarian neoplasm; Breast and/or ovarian cancer; Pancreatic cancer, susceptibility to, 4; Fanconi anemia, complementation group S; BRCA1-related cancer predisposition; Inherited ovarian cancer (without breast cancer); BRCA1-related disorder; Inherited breast cancer and ovarian cancer | germline/somatic | 69 | Aug 10, 2015 | clinvar |