Variant · Snv
PCNT NM_006031.6(PCNT):c.7536G>A (p.Pro2512=)
CI-VAR-00022490Explore in graph →p.Pro2512=NM_006031.6:c.7536G>AClinVar 138603 rs61735818
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 138603 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Microcephalic osteodysplastic primordial dwarfism type II; Colorectal cancer; Thymoma; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Uterine corpus endometrial carcinoma; Uveal melanoma; Uterine carcinosarcoma; Acute myeloid leukemia | germline | 6 | Feb 02, 2026 | clinvar |