Variant (rsID / SNP)
rs876660807
rs876660807 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53. Location: chromosome 17, position 7,577,566. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:7577566
- Cytoband
- 17p13.1
- HGVS
- NM_000546.6(TP53):c.715A>G (p.Asn239Asp)
- Allele change
- Missense_N107D
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Lung adenocarcinoma|Prostate adenocarcinoma|Malignant neoplasm of body of uterus|Uterine carcinosarcoma|Squamous cell carcinoma of the head and neck|Renal cell carcinoma, papillary, 1|Hepatocellular carcinoma|Ovarian serous cystadenocarcinoma|Gastric adenocarcinoma|Neoplasm of the large intestine|Breast neoplasm|Li-Fraumeni syndrome|Malignant tumor of breast
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.