Variant · Snv
UTP4 NM_032830.3(UTP4):c.1906C>T (p.Arg636Cys)
CI-VAR-00153861Explore in graph →p.Arg636CysNM_032830.3:c.1906C>TClinVar 887109 rs61185783
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 |
|---|---|---|---|---|---|---|---|---|
| 887109 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Hereditary North American Indian childhood cirrhosis; Uveal melanoma; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Colorectal cancer; Sarcoma; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Uterine carcinosarcoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Thymoma; Hepatocellular carcinoma | germline | 4 | Jan 28, 2026 | clinvar |