Variant · Snv
COG2 NM_007357.3(COG2):c.1036A>G (p.Ile346Val)
CI-VAR-00196012Explore in graph →p.Ile346ValNM_007357.3:c.1036A>GClinVar 1165357 rs11558606
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 |
|---|---|---|---|---|---|---|---|---|
| 1165357 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Congenital disorder of glycosylation, type IIq; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Colorectal cancer; Thymoma; Adrenocortical carcinoma, hereditary; Uterine carcinosarcoma; Cholangiocarcinoma; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uveal melanoma; Familial pancreatic carcinoma; Colon adenocarcinoma | germline | 5 | Feb 02, 2026 | clinvar |