Variant · Snv
TP53 G245S
CI-VAR-00001676Explore in graph →NP_000537.3:p.Gly245SerNM_000546.5:c.733G>AClinVar 12365 CIViC 879 rs28934575
Curated evidence
Evidence by cancer (7 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
- 25669829
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Malignant Colorectal Neoplasm1 | ||||||||
| TP53 R273C OR TP53 G245S OR TP53 R213* | Pazopanib + VorinostatCombination | Predictive | C | Supports Sensitivity Response | 2 | accepted | EID12732In the phase I study of pazopanib and vorinostat in 36 patients with advanced solid tumors, detection of hotspot TP53 mutation was associated with a higher rate of SD ≥6 months/PR, longer median PFS (… (full text at CIViC) PMID 25669829 · Fu et al., 2015 · Open in CIViC | civic |
| Malignant Neoplasm1 | ||||||||
| TP53 G245S | MDM2 Inhibitor AMGMDS3 | Predictive | D | Supports Resistance | 4 | accepted | EID4883Subset of 58 cancer cell lines with unaltered TP53 is sensitive to MDM2 Inhibitor AMGMDS3. None of 115 cancer cell lines with TP53 mutation and absence of WT allele are sensitive to MDM2 Inhibitor. TP… | |
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 12365 | Pathogenic | reviewed by expert panel | 3 | Li-fraumeni-like syndrome; Li-Fraumeni syndrome 1; Hereditary cancer-predisposing syndrome; Adenocarcinoma; Li-Fraumeni syndrome; Astrocytoma, anaplastic; Atypical teratoid rhabdoid tumor; Ovarian neoplasm; Familial ovarian cancer; Breast carcinoma; Colorectal cancer; Gastric cancer; Malignant tumor of urinary bladder; Adrenocortical carcinoma, hereditary; TP53-related disorder; Medulloblastoma WNT activated; Rhabdomyosarcoma; IDH-wildtype glioblastoma; Neoplasm |