NM_000314.8(PTEN):c.801+11T>C AND PTEN hamartoma tumor syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 27, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002943006.2
Allele description [Variation Report for NM_000314.8(PTEN):c.801+11T>C]
NM_000314.8(PTEN):c.801+11T>C
Condition(s)
- Name:
- PTEN hamartoma tumor syndrome (PHTS)
- Synonyms:
- PTEN Hamartomatous Tumour Syndrome; PTEN-related disorders
- Identifiers:
- MONDO: MONDO:0017623; MeSH: D006223; MedGen: C1959582
Assertion and evidence details
Last Updated: Feb 14, 2024