Variant · Other
IQCE NM_152558.5(IQCE):c.1350_1353del
CI-VAR-00113748Explore in graph →NM_152558.5:c.1350_1353delClinVar 638150 rs760694987
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 |
|---|---|---|---|---|---|---|---|---|
| 638150 | Pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Polydactyly, postaxial, type A1; Polydactyly, postaxial, type a7; IQCE-related disorder; Familial pancreatic carcinoma | germline | 8 | Jul 21, 2026 | clinvar |