Variant · Snv
OTUD4 NM_001366057.1(OTUD4):c.581C>G (p.Ala194Gly)
CI-VAR-00072092Explore in graph →p.Ala194GlyNM_001366057.1:c.581C>GClinVar 453300 rs36225458
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 |
|---|---|---|---|---|---|---|---|---|
| 453300 | Uncertain significance | criteria provided, single submitter | 1 | Thyroid cancer, nonmedullary, 1; Malignant lymphoma, large B-cell, diffuse; Acute myeloid leukemia; Hepatocellular carcinoma; Malignant tumor of esophagus; Cervical cancer; Familial cancer of breast | germline | 3 | — | clinvar |