Variant · Snv
CCDC88C NM_001080414.4(CCDC88C):c.1131C>T (p.Gly377=)
CI-VAR-00025093Explore in graph →p.Gly377=NM_001080414.4:c.1131C>TClinVar 158105 rs17127245
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 |
|---|---|---|---|---|---|---|---|---|
| 158105 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Malignant lymphoma, large B-cell, diffuse; Uterine corpus endometrial carcinoma; Colorectal cancer; Thymoma; Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia | germline | 6 | Feb 04, 2026 | clinvar |