Variant · Snv
ATP6V1E1 NM_001696.4(ATP6V1E1):c.528C>T (p.Asp176=)
CI-VAR-00127309Explore in graph →p.Asp176=NM_001696.4:c.528C>TClinVar 789862 rs73391487
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 |
|---|---|---|---|---|---|---|---|---|
| 789862 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Uterine carcinosarcoma; Melanoma; Thyroid cancer, nonmedullary, 1; Cholangiocarcinoma; Familial cancer of breast; Clear cell carcinoma of kidney; Uveal melanoma; Colon adenocarcinoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Lung cancer; Cervical cancer | germline | 6 | Feb 02, 2026 | clinvar |