NM_018127.7(ELAC2):c.1479G>A (p.Pro493=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 24, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000425836.1
Allele description [Variation Report for NM_018127.7(ELAC2):c.1479G>A (p.Pro493=)]
NM_018127.7(ELAC2):c.1479G>A (p.Pro493=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024