Variant · Snv
MOCS1 NM_001358530.2(MOCS1):c.1355G>T (p.Arg452Leu)
CI-VAR-00051557Explore in graph →p.Arg452LeuNM_001358530.2:c.1355G>TClinVar 356648 rs11969206
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 |
|---|---|---|---|---|---|---|---|---|
| 356648 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A; Adrenocortical carcinoma, hereditary; Lung cancer; Thymoma; Malignant tumor of esophagus; Colon adenocarcinoma; Sarcoma; Gastric cancer; Cholangiocarcinoma | germline | 4 | Feb 04, 2026 | clinvar |