NM_020340.5(ARFGEF3):c.1896G>A (p.Ser632=) AND ARFGEF3-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 26, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003932255.1
Allele description [Variation Report for NM_020340.5(ARFGEF3):c.1896G>A (p.Ser632=)]
NM_020340.5(ARFGEF3):c.1896G>A (p.Ser632=)
Condition(s)
- Name:
- ARFGEF3-related disorder
- Synonyms:
- ARFGEF3-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024