NM_000530.8(MPZ):c.51G>A (p.Leu17=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 14, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000612080.1
Allele description [Variation Report for NM_000530.8(MPZ):c.51G>A (p.Leu17=)]
NM_000530.8(MPZ):c.51G>A (p.Leu17=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024