NM_001126049.2(KLLN):c.-1007C>G AND PTEN hamartoma tumor syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 25, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000790889.10
Allele description [Variation Report for NM_001126049.2(KLLN):c.-1007C>G]
NM_001126049.2(KLLN):c.-1007C>G
Condition(s)
- Name:
- PTEN hamartoma tumor syndrome (PHTS)
- Synonyms:
- PTEN Hamartomatous Tumour Syndrome
- Identifiers:
- MONDO: MONDO:0017623; MeSH: D006223; MedGen: C1959582
Assertion and evidence details
Last Updated: Aug 25, 2024