Variant · Snv
ADAP1 NM_006869.4(ADAP1):c.389-8C>G
CI-VAR-00132147Explore in graph →NM_006869.4:c.389-8C>GClinVar 774872 rs150718412
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 774872 | Benign | criteria provided, single submitter | 1 | Uterine corpus endometrial carcinoma; Uveal melanoma; Thyroid cancer, nonmedullary, 1; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Lung cancer; Familial pancreatic carcinoma; Gastric cancer; Familial cancer of breast; Sarcoma; Uterine carcinosarcoma; Cervical cancer | germline | 2 | Jun 18, 2018 | clinvar |