Variant (rsID / SNP)
rs876660333
rs876660333 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53. Location: chromosome 17, position 7,577,123. Clinical significance in the table: Uncertain significance.
Reference-table entries
- Clinical significance (as recorded)
- Uncertain significance
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:7577123
- Cytoband
- 17p13.1
- HGVS
- NM_000546.6(TP53):c.815T>G (p.Val272Gly)
- Allele change
- Missense_V140G
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Ovarian serous cystadenocarcinoma|Gastric adenocarcinoma|Transitional cell carcinoma of the bladder|Malignant neoplasm of body of uterus|Breast neoplasm|Multiple myeloma|Neoplasm of the large intestine|Lung adenocarcinoma|Pancreatic adenocarcinoma|Renal cell carcinoma, papillary, 1|Medulloblastoma|Squamous cell carcinoma of the skin|Squamous cell carcinoma of the head and neck
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.