NM_012414.4(RAB3GAP2):c.1344T>C (p.Asp448=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002889236.3
Allele description [Variation Report for NM_012414.4(RAB3GAP2):c.1344T>C (p.Asp448=)]
NM_012414.4(RAB3GAP2):c.1344T>C (p.Asp448=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024