Variant (rsID / SNP)

rs587781589

rs587781589 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53. Location: chromosome 17, position 7,577,586. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

TP53Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 17:7577586
Cytoband: 17p13.1
HGVS: NM_000546.6(TP53):c.695T>C (p.Ile232Thr)
Allele change: Missense_I100T

Associated conditions / phenotypes

Hereditary cancer-predisposing syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.