Variant · Snv
PTGS1 NM_000962.4(PTGS1):c.123G>A (p.Gln41=)
CI-VAR-00199493Explore in graph →p.Gln41=NM_000962.4:c.123G>AClinVar 1241842 rs3842788
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 |
|---|---|---|---|---|---|---|---|---|
| 1241842 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Colon adenocarcinoma; Lymphoma; Malignant tumor of esophagus; Ovarian cancer; Thymoma; Melanoma; Cholangiocarcinoma; Acute myeloid leukemia; Colorectal cancer; Uterine carcinosarcoma; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Familial pancreatic carcinoma | germline | 4 | Sep 29, 2022 | clinvar |