Variant · Snv
NLRP1 NM_033004.4(NLRP1):c.2841G>C (p.Arg947Ser)
CI-VAR-00127745Explore in graph →p.Arg947SerNM_033004.4:c.2841G>CClinVar 714854 rs143175019
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 |
|---|---|---|---|---|---|---|---|---|
| 714854 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome; Autoinflammation with arthritis and dyskeratosis; Vitiligo-associated multiple autoimmune disease susceptibility 1; Respiratory papillomatosis, juvenile recurrent, congenital | germline | 2 | Nov 03, 2025 | clinvar |