Variant · Snv
IL4R NM_000418.4(IL4R):c.822C>G (p.Leu274=)
CI-VAR-00127709Explore in graph →p.Leu274=NM_000418.4:c.822C>GClinVar 710743 rs2234896
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 |
|---|---|---|---|---|---|---|---|---|
| 710743 | Benign | criteria provided, single submitter | 1 | Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Melanoma; Thymoma; Malignant tumor of urinary bladder; Hepatocellular carcinoma; Malignant tumor of esophagus; Cervical cancer; Familial cancer of breast; Colon adenocarcinoma; Colorectal cancer; Sarcoma; Gastric cancer | germline | 2 | Apr 16, 2018 | clinvar |