Variant · Snv
COA6 NM_001206641.3(COA6):c.212+162G>A
CI-VAR-00093222Explore in graph →NM_001206641.3:c.212+162G>AClinVar 506397 rs113627094
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 |
|---|---|---|---|---|---|---|---|---|
| 506397 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4; Hepatocellular carcinoma; Malignant tumor of esophagus; Cervical cancer; Clear cell carcinoma of kidney; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Thymoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Uterine carcinosarcoma; Thyroid cancer, nonmedullary, 1 | germline | 5 | Dec 30, 2025 | clinvar |