Variant · Snv
MECOM NM_004991.4(MECOM):c.1418A>G (p.Asn473Ser)
CI-VAR-00287507Explore in graph →p.Asn473SerNM_004991.4:c.1418A>GClinVar 2071251 rs201542000
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 2071251 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Inborn genetic diseases; Clear cell carcinoma of kidney | germline | 3 | Nov 01, 2025 | clinvar |