NM_018161.5(NADSYN1):c.1132G>A (p.Glu378Lys) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003309359.2
Allele description [Variation Report for NM_018161.5(NADSYN1):c.1132G>A (p.Glu378Lys)]
NM_018161.5(NADSYN1):c.1132G>A (p.Glu378Lys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024