Variant · Snv
LZTR1 NM_006767.4(LZTR1):c.2462T>C (p.Ile821Thr)
CI-VAR-00113708Explore in graph →p.Ile821ThrNM_006767.4:c.2462T>CClinVar 635756 rs1275511136
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 |
|---|---|---|---|---|---|---|---|---|
| 635756 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Noonan syndrome 2; LZTR1-related schwannomatosis; Hereditary cancer-predisposing syndrome; Cardiovascular phenotype; LZTR1-related disorder; Noonan syndrome 1 | germline | 8 | Sep 19, 2025 | clinvar |