Variant (rsID / SNP)
rs765848205
rs765848205 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53. Location: chromosome 17, position 7,577,571. Clinical significance in the table: Likely pathogenic.
Reference-table entries
TP53Likely pathogenic
- Clinical significance (as recorded)
- Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:7577571
- Cytoband
- 17p13.1
- HGVS
- NM_000546.6(TP53):c.710T>A (p.Met237Lys)
- Allele change
- Missense_M105K
Associated conditions / phenotypes
Squamous cell lung carcinoma|Malignant neoplasm of body of uterus|Squamous cell carcinoma of the head and neck|Gastric adenocarcinoma|Pancreatic adenocarcinoma|Neoplasm of brain|Lung adenocarcinoma|Breast neoplasm|Brainstem glioma|Carcinoma of esophagus|Neoplasm of the large intestine|Ovarian serous cystadenocarcinoma
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.