Variant · Snv
RNF213 NM_001256071.3(RNF213):c.13510+4A>G
CI-VAR-00127994Explore in graph →NM_001256071.3:c.13510+4A>GClinVar 713384 rs139279361
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 |
|---|---|---|---|---|---|---|---|---|
| 713384 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Cervical cancer; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Colon adenocarcinoma; Colorectal cancer; Sarcoma; Gastric cancer; Uterine corpus endometrial carcinoma; Melanoma; Malignant tumor of esophagus; Familial cancer of breast | germline | 6 | May 01, 2026 | clinvar |