Variant · Snv
PDGFRB NM_002609.4(PDGFRB):c.85A>T (p.Ile29Phe)
CI-VAR-00047217Explore in graph →p.Ile29PheNM_002609.4:c.85A>TClinVar 258780 rs17110944
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 258780 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Basal ganglia calcification, idiopathic, 4; Skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome; Acroosteolysis-keloid-like lesions-premature aging syndrome; Infantile myofibromatosis; Myeloproliferative disorder, chronic, with eosinophilia; PDGFRB-related disorder; Myofibromatosis, infantile, 1; Cholangiocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Sarcoma; Thymoma; Colon adenocarcinoma; Uterine carcinosarcoma; Thyroid cancer, nonmedullary, 1; Lung cancer | germline | 8 | Feb 01, 2026 | clinvar |