NM_001370298.3(FGD4):c.1470C>T (p.Pro490=) AND FGD4-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 5, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003940176.1
Allele description [Variation Report for NM_001370298.3(FGD4):c.1470C>T (p.Pro490=)]
NM_001370298.3(FGD4):c.1470C>T (p.Pro490=)
Condition(s)
- Name:
- FGD4-related disorder
- Synonyms:
- FGD4-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 26, 2024