Variant · Snv
PLS3 NM_005032.7(PLS3):c.925A>G (p.Ile309Val)
CI-VAR-00198181Explore in graph →p.Ile309ValNM_005032.7:c.925A>GClinVar 1206375 rs140968059
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 |
|---|---|---|---|---|---|---|---|---|
| 1206375 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Osteogenesis imperfecta; PLS3-related disorder; Uterine corpus endometrial carcinoma; Sarcoma; Gastric cancer; Adrenocortical carcinoma, hereditary; Cervical cancer; Thyroid cancer, nonmedullary, 1; Lung cancer | germline | 10 | Feb 01, 2026 | clinvar |