Variant · Snv
CEP164 NM_014956.5(CEP164):c.2205C>T (p.Ser735=)
CI-VAR-00047383Explore in graph →p.Ser735=NM_014956.5:c.2205C>TClinVar 260478 rs494553
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 |
|---|---|---|---|---|---|---|---|---|
| 260478 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Nephronophthisis 15; Thymoma; Cholangiocarcinoma; Colorectal cancer; Melanoma; Acute myeloid leukemia; Hepatocellular carcinoma; Adrenocortical carcinoma, hereditary; Uterine corpus endometrial carcinoma; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma | germline | 7 | Feb 02, 2026 | clinvar |