Variant · Snv
OGG1 NM_002542.6(OGG1):c.137G>A (p.Arg46Gln)
CI-VAR-00005712Explore in graph →p.Arg46GlnNM_002542.6:c.137G>AClinVar 7602 rs104893751
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 7602 | Uncertain significance | criteria provided, single submitter | 1 | Clear cell carcinoma of kidney; Cholangiocarcinoma; Malignant tumor of urinary bladder; Hepatocellular carcinoma; Malignant tumor of esophagus; Lung cancer; Uveal melanoma; Thymoma; Melanoma; Colon adenocarcinoma; Colorectal cancer; Sarcoma; Gastric cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Familial cancer of breast | germline/somatic | 5 | Jul 31, 2021 | clinvar |