NM_144573.4(NEXN):c.1432G>A (p.Asp478Asn) AND Cardiovascular phenotype
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 4, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000618386.3
Allele description [Variation Report for NM_144573.4(NEXN):c.1432G>A (p.Asp478Asn)]
NM_144573.4(NEXN):c.1432G>A (p.Asp478Asn)
Condition(s)
- Name:
- Cardiovascular phenotype
- Identifiers:
- MedGen: CN230736
Assertion and evidence details
Last Updated: Sep 29, 2024