Variant · Snv
CTCF NM_006565.4(CTCF):c.1164C>T (p.Ser388=)
CI-VAR-00020371Explore in graph →p.Ser388=NM_006565.4:c.1164C>TClinVar 128863 rs143837268
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 |
|---|---|---|---|---|---|---|---|---|
| 128863 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Inborn genetic diseases; Uterine corpus endometrial carcinoma; Malignant lymphoma, large B-cell, diffuse; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Cholangiocarcinoma; Cervical cancer; Uveal melanoma; Thymoma; Melanoma; Colon adenocarcinoma; Colorectal cancer; Sarcoma; Gastric cancer; Acute myeloid leukemia; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Lung cancer | germline | 5 | Aug 31, 2018 | clinvar |