Variant · Snv
MET NM_000245.4(MET):c.632T>G (p.Leu211Trp)
CI-VAR-00033675Explore in graph →p.Leu211TrpNM_000245.4:c.632T>GClinVar 216513 rs45483396
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 |
|---|---|---|---|---|---|---|---|---|
| 216513 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Papillary renal cell carcinoma type 1; Hereditary cancer-predisposing syndrome; Renal cell carcinoma; Hepatocellular carcinoma; Osteofibrous dysplasia; Autosomal recessive nonsyndromic hearing loss 97; Arthrogryposis, distal, IIa 11 | germline | 7 | Feb 03, 2026 | clinvar |