Variant · Snv
TP53 NM_000546.6(TP53):c.413C>T (p.Ala138Val)
CI-VAR-00030886Explore in graph →p.Ala138ValNM_000546.6:c.413C>TClinVar 184863 rs750600586
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 |
|---|---|---|---|---|---|---|---|---|
| 184863 | Likely pathogenic | reviewed by expert panel | 3 | Hereditary cancer-predisposing syndrome; Li-Fraumeni syndrome; Adrenocortical carcinoma, hereditary; Li-Fraumeni syndrome 1; Adrenal cortex carcinoma; Choroid plexus carcinoma; Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype; Neoplasm | germline/somatic | 8 | Jun 05, 2025 | clinvar |