NM_015213.4(DENND5A):c.427A>G (p.Ser143Gly) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 21, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002718044.2
Allele description [Variation Report for NM_015213.4(DENND5A):c.427A>G (p.Ser143Gly)]
NM_015213.4(DENND5A):c.427A>G (p.Ser143Gly)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024