Variant · Snv
ITGB4 NM_000213.5(ITGB4):c.194C>T (p.Ala65Val)
CI-VAR-00294377Explore in graph →p.Ala65ValNM_000213.5:c.194C>TClinVar 2349947 rs200966154
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 |
|---|---|---|---|---|---|---|---|---|
| 2349947 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Inborn genetic diseases; ITGB4-related disorder; Epidermolysis bullosa, junctional 5A, intermediate; Junctional epidermolysis bullosa with pyloric atresia; Papillary renal cell carcinoma type 1 | germline | 4 | Apr 01, 2024 | clinvar |