NM_012414.4(RAB3GAP2):c.2168T>A (p.Val723Glu) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000540400.10
Allele description [Variation Report for NM_012414.4(RAB3GAP2):c.2168T>A (p.Val723Glu)]
NM_012414.4(RAB3GAP2):c.2168T>A (p.Val723Glu)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024