Variant · Snv
UTP18 NM_016001.3(UTP18):c.1534A>G (p.Asn512Asp)
CI-VAR-00293766Explore in graph →p.Asn512AspNM_016001.3:c.1534A>GClinVar 2213182 rs191307031
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 2213182 | Uncertain significance | criteria provided, single submitter | 1 | Melanoma; Malignant tumor of esophagus; Clear cell carcinoma of kidney; Uveal melanoma; Thyroid cancer, nonmedullary, 1; Malignant tumor of urinary bladder; Lung cancer; Cervical cancer; Familial cancer of breast | germline | 2 | Apr 08, 2022 | clinvar |