Variant · Snv
PEX5 NM_001351132.2(PEX5):c.*75G>A
CI-VAR-00052856Explore in graph →NM_001351132.2:c.*75G>AClinVar 310437 rs112966367
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 |
|---|---|---|---|---|---|---|---|---|
| 310437 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Peroxisome biogenesis disorder 2A (Zellweger); Malignant tumor of esophagus; Thymoma; Uterine corpus endometrial carcinoma | germline | 4 | Aug 18, 2021 | clinvar |