Variant · Snv
PCNT NM_006031.6(PCNT):c.7652C>T (p.Ala2551Val)
CI-VAR-00022491Explore in graph →p.Ala2551ValNM_006031.6:c.7652C>TClinVar 138605 rs12481791
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 |
|---|---|---|---|---|---|---|---|---|
| 138605 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Microcephalic osteodysplastic primordial dwarfism type II; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer; Melanoma; Hepatocellular carcinoma; Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Thymoma; Uveal melanoma; Colon adenocarcinoma; Thyroid cancer, nonmedullary, 1; Cholangiocarcinoma; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Malignant tumor of esophagus; Adrenocortical carcinoma, hereditary; Lung cancer; Cervical cancer | germline | 12 | Jun 01, 2026 | clinvar |