Variant · Snv
WDR19 NM_025132.4(WDR19):c.2361C>T (p.Phe787=)
CI-VAR-00049796Explore in graph →p.Phe787=NM_025132.4:c.2361C>TClinVar 287684 rs200133722
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 |
|---|---|---|---|---|---|---|---|---|
| 287684 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Cranioectodermal dysplasia 4; Asphyxiating thoracic dystrophy 5; Senior-Loken syndrome 8; Connective tissue disorder; Clear cell carcinoma of kidney; Colorectal cancer; Ovarian serous cystadenocarcinoma; Glioma susceptibility 1; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Lung cancer; Cervical cancer; Familial cancer of breast | germline | 10 | Jan 26, 2026 | clinvar |