Variant · Snv
IFT172 NM_015662.3(IFT172):c.337-5C>T
CI-VAR-00238619Explore in graph →NM_015662.3:c.337-5C>TClinVar 1572647 rs141086523
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 |
|---|---|---|---|---|---|---|---|---|
| 1572647 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Short-rib thoracic dysplasia 10 with or without polydactyly; Retinitis pigmentosa 71; Inborn genetic diseases; IFT172-related disorder; Familial cancer of breast | germline | 5 | Aug 12, 2025 | clinvar |