Variant · Snv
IFT43 NM_001102564.3(IFT43):c.296-5602T>C
CI-VAR-00109745Explore in graph →NM_001102564.3:c.296-5602T>CClinVar 596041 rs141114765
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 |
|---|---|---|---|---|---|---|---|---|
| 596041 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Retinitis pigmentosa 81; Connective tissue disorder; Short-rib thoracic dysplasia 18 with polydactyly; Cranioectodermal dysplasia 3; Uterine carcinosarcoma | germline | 8 | Jan 05, 2026 | clinvar |