Variant · Deletion
COL7A1 NM_000094.4(COL7A1):c.7984-7del
CI-VAR-00051016Explore in graph →NM_000094.4:c.7984-7delClinVar 345801 rs66737445
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 |
|---|---|---|---|---|---|---|---|---|
| 345801 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Epidermolysis bullosa dystrophica; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Gastric cancer; Malignant tumor of esophagus; Ovarian cancer; Colorectal cancer; Hepatocellular carcinoma | germline | 5 | Feb 04, 2026 | clinvar |