Variant · Snv
COX10 NM_001303.4(COX10):c.184A>T (p.Thr62Ser)
CI-VAR-00022330Explore in graph →p.Thr62SerNM_001303.4:c.184A>TClinVar 137006 rs2230351
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 |
|---|---|---|---|---|---|---|---|---|
| 137006 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Leigh syndrome; Mitochondrial complex IV deficiency, nuclear type 1; Thymoma; Cholangiocarcinoma; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Malignant lymphoma, large B-cell, diffuse; Uterine carcinosarcoma; Uterine corpus endometrial carcinoma; Colorectal cancer | germline | 6 | Feb 02, 2026 | clinvar |