Variant · Snv
TP53 R273L
CI-VAR-00003802Explore in graph →NP_000537.3:p.Arg273LeuNM_000546.5:c.818G>TClinVar 376655 CIViC 918 rs28934576
Curated evidence
Evidence by cancer (3 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.
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 11595686
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Ovarian Neoplasm1 | ||||||||
| TP53 R273L | Carboplatin + CisplatinSubstitutes | Predictive | C | Supports Resistance | — | accepted | EID2286Ovarian cancer patients with TP53 missense mutations were refractory to platinum-based chemotherapy (66% vs. 34% in wildtype, P=0.008) and had a shorter time to disease progression (n=54, P=0.037). A … (full text at CIViC) PMID 11595686 · Reles et al., 2001 · Open in CIViC | civic |
| Unmapped disease2unmapped disease | ||||||||
| TP53 R273L | (functional) | Functional | D | Supports Dominant Negative | 3 | submitted | EID10538Yeast strain yIG397 was cultured to express both wild-type (WT) and mutant R273L originally identified in an oral lesion. Should the mutant be dominant-negative (DN), TP53 will not bind and transactiv… | |
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
- 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 |
|---|---|---|---|---|---|---|---|---|
| 376655 | Pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Ovarian neoplasm; Li-Fraumeni syndrome; Hereditary cancer-predisposing syndrome; Li-Fraumeni syndrome 1; Neoplasm; Neuroendocrine tumor of pancreas; Embryonal rhabdomyosarcoma | germline/somatic | 10 | May 11, 2025 | clinvar |