Variant · Snv
SUOX NM_001032386.2(SUOX):c.228G>T (p.Arg76Ser)
CI-VAR-00052823Explore in graph →p.Arg76SerNM_001032386.2:c.228G>TClinVar 309833 rs202085145
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 |
|---|---|---|---|---|---|---|---|---|
| 309833 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Sulfite oxidase deficiency; Inborn genetic diseases; SUOX-related disorder; Ovarian serous cystadenocarcinoma; Uterine carcinosarcoma; Malignant tumor of urinary bladder; Thyroid cancer, nonmedullary, 1; Clear cell carcinoma of kidney; Gastric cancer; Nonpapillary renal cell carcinoma | germline | 10 | Jan 28, 2026 | clinvar |