Variant · Snv
INF2 NM_022489.4(INF2):c.2630G>A (p.Arg877Gln)
CI-VAR-00047459Explore in graph →p.Arg877GlnNM_022489.4:c.2630G>AClinVar 261610 rs142678449
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 |
|---|---|---|---|---|---|---|---|---|
| 261610 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Focal segmental glomerulosclerosis 5; Charcot-Marie-Tooth disease dominant intermediate E; Uterine corpus endometrial carcinoma; Sarcoma; Uterine carcinosarcoma; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary; Ovarian serous cystadenocarcinoma; Thymoma; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Lung cancer; Clear cell carcinoma of kidney; Thyroid cancer, nonmedullary, 1; Melanoma; Uveal melanoma; Colon adenocarcinoma; Cholangiocarcinoma; Acute myeloid leukemia; Colorectal cancer; Cervical cancer; Familial cancer of breast | germline | 14 | Jul 01, 2026 | clinvar |