Variant · Snv
VCP NM_007126.5(VCP):c.1360-14C>G
CI-VAR-00047316Explore in graph →NM_007126.5:c.1360-14C>GClinVar 260122 rs144304208
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 |
|---|---|---|---|---|---|---|---|---|
| 260122 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1; Frontotemporal dementia and/or amyotrophic lateral sclerosis 6; Inclusion body myopathy with Paget disease of bone and frontotemporal dementia; Uveal melanoma; Ovarian cancer; Gastric cancer; Familial cancer of breast; Lymphoma; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma; Cervical cancer | germline | 10 | Jun 01, 2026 | clinvar |