Variant · Snv
MET NM_000245.4(MET):c.1285T>A (p.Leu429Ile)
CI-VAR-00061038Explore in graph →p.Leu429IleNM_000245.4:c.1285T>AClinVar 411885 rs911380470
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 |
|---|---|---|---|---|---|---|---|---|
| 411885 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Hereditary cancer-predisposing syndrome; Renal cell carcinoma; Osteofibrous dysplasia; Hepatocellular carcinoma; Autosomal recessive nonsyndromic hearing loss 97; Arthrogryposis, distal, IIa 11; Papillary renal cell carcinoma type 1 | germline | 4 | Mar 04, 2025 | clinvar |