Variant · Snv
CCDC18 NM_001378204.1(CCDC18):c.3324G>T (p.Arg1108Ser)
CI-VAR-00339295Explore in graph →p.Arg1108SerNM_001378204.1:c.3324G>TClinVar 3055670 rs61729705
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 3055670 | Benign | no assertion criteria provided | 0 | CCDC18-related disorder; Sarcoma; Ovarian serous cystadenocarcinoma; Lung cancer; Familial pancreatic carcinoma; Thymoma; Acute myeloid leukemia; Hepatocellular carcinoma; Malignant tumor of esophagus; Colon adenocarcinoma; Gastric cancer; Uterine carcinosarcoma; Nonpapillary renal cell carcinoma; Cervical cancer | germline | 2 | Apr 09, 2019 | clinvar |