NM_000311.5(PRNP):c.159C>T (p.Gly53=) AND Inherited prion disease
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000287805.5
Allele description [Variation Report for NM_000311.5(PRNP):c.159C>T (p.Gly53=)]
NM_000311.5(PRNP):c.159C>T (p.Gly53=)
Condition(s)
- Name:
- Inherited prion disease
- Identifiers:
- MedGen: C5679775
Assertion and evidence details
Last Updated: Sep 29, 2024