Variant (rsID / SNP)
rs149633775
rs149633775 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53. Location: chromosome 17, position 7,577,091. Clinical significance in the table: Likely benign.
Reference-table entries
TP53Likely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:7577091
- Cytoband
- 17p13.1
- HGVS
- NM_000546.6(TP53):c.847C>T (p.Arg283Cys)
- Allele change
- Missense_R151C
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Neoplasm of stomach|Li-Fraumeni syndrome|Li-Fraumeni syndrome 1|11 conditions|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.