Variant · Snv
FLNC NM_001458.5(FLNC):c.4022G>A (p.Arg1341Gln)
CI-VAR-00031726Explore in graph →p.Arg1341GlnNM_001458.5:c.4022G>AClinVar 195741 rs149641783
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 |
|---|---|---|---|---|---|---|---|---|
| 195741 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Cardiovascular phenotype; Cardiomyopathy; FLNC-related disorder; Clear cell carcinoma of kidney; Lung cancer; Hypertrophic cardiomyopathy 26; Distal myopathy with posterior leg and anterior hand involvement; Myofibrillar myopathy 5; Sarcoma; Cervical cancer | germline | 16 | Jun 01, 2026 | clinvar |