Variant · Snv
ARMC5 NM_001105247.2(ARMC5):c.2058G>A (p.Ala686=)
CI-VAR-00338943Explore in graph →p.Ala686=NM_001105247.2:c.2058G>AClinVar 3037824 rs11863886
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 |
|---|---|---|---|---|---|---|---|---|
| 3037824 | Likely benign | criteria provided, single submitter | 1 | ARMC5-related disorder; Uterine carcinosarcoma; Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia; Hepatocellular carcinoma; Malignant lymphoma, large B-cell, diffuse; Gastric cancer; Lung cancer; Sarcoma; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Cervical cancer | germline | 3 | Nov 27, 2024 | clinvar |