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rs28934574

NM_000546.6(TP53):c.844C>T (p.Arg282Trp)

TP53missense variantp.Arg282Trpsingle nucleotide variant
ClinVar by condition
  • Li-Fraumeni syndrome (LFS)Pathogenic · ★★ · unknown
  • Hereditary cancer-predisposing syndromeLikely pathogenic · ★★ · germline
  • Li-Fraumeni syndrome 1 (LFS)Likely pathogenic · ★★ · germline
  • Adrenocortical carcinoma, hereditary (ADCC)Pathogenic · ★ · unknown
  • Astrocytoma, anaplasticPathogenic · ★ · germline
  • Pleomorphic xanthoastrocytoma (PXA)Pathogenic · ★ · germline
  • Squamous cell carcinoma of the head and neck (HNSCC)Pathogenic · ★ · somatic
  • Colorectal cancerPathogenic · ★ · somatic
  • Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtypeLikely pathogenic · ★ · germline
  • TP53-related disorderPathogenic · germline
  • Li-fraumeni-like syndromePathogenic · germline
  • Ovarian neoplasmLikely pathogenic · somatic

rs28934574 is a genetic variant located in the TP53 gene. dbsnp · gene

In ClinVar, rs28934574 is classified as Pathogenic for Li-Fraumeni syndrome (LFS) (2 review stars; last evaluated 2025-02-03). clinvar · classificationclinvar · review confidenceclinvar · assertion date

In ClinVar, rs28934574 is classified as Likely pathogenic for Hereditary cancer-predisposing syndrome (2 review stars, germline; last evaluated 2024-07-05). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date

In ClinVar, rs28934574 is classified as Likely pathogenic for Li-Fraumeni syndrome 1 (LFS) (2 review stars, germline; last evaluated 2023-07-07). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date

In ClinVar, rs28934574 is classified as Pathogenic for Adrenocortical carcinoma, hereditary (ADCC) (1 review star; last evaluated 2024-02-14). clinvar · classificationclinvar · review confidenceclinvar · assertion date

In ClinVar, rs28934574 is classified as Pathogenic for Astrocytoma, anaplastic (1 review star, germline; last evaluated 2016-11-04). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date

In ClinVar, rs28934574 is classified as Pathogenic for Pleomorphic xanthoastrocytoma (PXA) (1 review star, germline; last evaluated 2016-11-04). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date

In ClinVar, rs28934574 is classified as Pathogenic for Squamous cell carcinoma of the head and neck (HNSCC) (1 review star, somatic). clinvar · classificationclinvar · review confidenceclinvar · origin

In ClinVar, rs28934574 is classified as Pathogenic for Colorectal cancer (1 review star, somatic). clinvar · classificationclinvar · review confidenceclinvar · origin

In ClinVar, rs28934574 is classified as Likely pathogenic for Diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype (1 review star, germline; last evaluated 2019-02-12). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date

In ClinVar, rs28934574 is classified as Pathogenic for TP53-related disorder (0 review stars, germline; last evaluated 2024-10-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date

In ClinVar, rs28934574 is classified as Pathogenic for Li-fraumeni-like syndrome (0 review stars, germline; last evaluated 1995-01-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date

In ClinVar, rs28934574 is classified as Likely pathogenic for Ovarian neoplasm (0 review stars, somatic; last evaluated 2018-12-01). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date

In ClinVar, rs28934574 is classified as Pathogenic for not provided (2 review stars, germline; last evaluated 2021-05-21). clinvar · classificationclinvar · review confidenceclinvar · originclinvar · assertion date

Sources

retrieved 2026-08-03 · facts 6363a9313da8fcc6 · meta/llama-3.1-8b-instruct · prompt 4.0.1 · schema 3.0.0

Educational information only — not medical advice, a diagnosis, or a clinical interpretation. A variant's significance can be uncertain, conflicting, or dependent on your full clinical and family context. Consult a qualified genetics professional or genetic counselor before drawing any conclusion.