Variant · Snv
STRADA NM_001003787.4(STRADA):c.508C>G (p.Leu170Val)
CI-VAR-00080051Explore in graph →p.Leu170ValNM_001003787.4:c.508C>GClinVar 468884 rs61734984
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 |
|---|---|---|---|---|---|---|---|---|
| 468884 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Polyhydramnios, megalencephaly, and symptomatic epilepsy; STRADA-related disorder; Uterine corpus endometrial carcinoma | germline | 4 | Mar 01, 2026 | clinvar |