Variant · Snv
TP53 NM_000546.6(TP53):c.991C>T (p.Gln331Ter)
CI-VAR-00158150Explore in graph →p.Gln331TerNM_000546.6:c.991C>TClinVar 922893 rs1597359130
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 |
|---|---|---|---|---|---|---|---|---|
| 922893 | Pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Hereditary cancer-predisposing syndrome; Malignant tumor of urinary bladder; Li-Fraumeni syndrome; Li-Fraumeni syndrome 1; Neoplasm; Squamous cell carcinoma of the head and neck; Melanoma; Lung cancer; Familial cancer of breast; Uterine corpus endometrial carcinoma; Mesothelioma | germline/somatic | 8 | Dec 29, 2025 | clinvar |