NM_000018.4(ACADVL):c.1575C>A (p.Val525=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 8, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002391010.3
Allele description [Variation Report for NM_000018.4(ACADVL):c.1575C>A (p.Val525=)]
NM_000018.4(ACADVL):c.1575C>A (p.Val525=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 20, 2024