Variant · Deletion
PCNT NM_006031.6(PCNT):c.4792-6del
CI-VAR-00237108Explore in graph →NM_006031.6:c.4792-6delClinVar 1662615 rs575429540
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 |
|---|---|---|---|---|---|---|---|---|
| 1662615 | Benign | criteria provided, single submitter | 1 | Uterine corpus endometrial carcinoma; Uveal melanoma; Familial cancer of breast; Malignant lymphoma, large B-cell, diffuse; Gastric cancer | germline | 2 | Jan 01, 2026 | clinvar |