Variant · Snv
CEP63 NM_001353108.3(CEP63):c.555G>C (p.Gln185His)
CI-VAR-00020359Explore in graph →p.Gln185HisNM_001353108.3:c.555G>CClinVar 128709 rs114108011
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 |
|---|---|---|---|---|---|---|---|---|
| 128709 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Lymphoma; Uterine carcinosarcoma; Thymoma; Thyroid cancer, nonmedullary, 1; Uveal melanoma; Colon adenocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus; Familial cancer of breast; Familial pancreatic carcinoma; Sarcoma; Cholangiocarcinoma; Hepatocellular carcinoma; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Cervical cancer | germline | 7 | Apr 01, 2026 | clinvar |