Variant · Snv
MEN1 NM_001370259.2(MEN1):c.1003C>A (p.Arg335=)
CI-VAR-00047407Explore in graph →p.Arg335=NM_001370259.2:c.1003C>AClinVar 255616 rs371364206
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 |
|---|---|---|---|---|---|---|---|---|
| 255616 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Multiple endocrine neoplasia, type 1; Hereditary cancer-predisposing syndrome; Hyperparathyroidism; Malignant tumor of esophagus; Malignant tumor of urinary bladder | germline | 11 | Jan 27, 2026 | clinvar |