Variant · Snv
FLCN NM_144997.7(FLCN):c.113G>T (p.Ser38Ile)
CI-VAR-00064369Explore in graph →p.Ser38IleNM_144997.7:c.113G>TClinVar 409391 rs139418842
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 |
|---|---|---|---|---|---|---|---|---|
| 409391 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Birt-Hogg-Dube syndrome; Hereditary cancer-predisposing syndrome; Familial spontaneous pneumothorax; 17p11.2 microduplication syndrome; Colorectal cancer; Nonpapillary renal cell carcinoma; FLCN-related disorder; Birt-Hogg-Dube syndrome 1 | germline | 8 | Jan 27, 2026 | clinvar |