Variant (rsID / SNP)

rs139767111

rs139767111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTEN. Location: chromosome 10, position 89,692,871. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

PTENLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 10:89692871
Cytoband: 10q23.31
HGVS: NM_000314.8(PTEN):c.355G>C (p.Val119Leu)
Allele change: Missense_V292L

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.