Variant · Snv
PNPT1 NM_033109.5(PNPT1):c.223-65G>T
CI-VAR-00122699Explore in graph →NM_033109.5:c.223-65G>TClinVar 676180 rs72807624
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 |
|---|---|---|---|---|---|---|---|---|
| 676180 | Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Gastric cancer; Lymphoma; Uterine carcinosarcoma; Thymoma; Familial pancreatic carcinoma; Sarcoma; Malignant tumor of esophagus; Lung cancer; Uterine corpus endometrial carcinoma; Ovarian cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Malignant lymphoma, large B-cell, diffuse; Nonpapillary renal cell carcinoma; Cervical cancer | germline | 3 | Jun 13, 2018 | clinvar |