NM_012414.4(RAB3GAP2):c.3978G>T (p.Glu1326Asp) AND Martsolf syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000305520.5
Allele description [Variation Report for NM_012414.4(RAB3GAP2):c.3978G>T (p.Glu1326Asp)]
NM_012414.4(RAB3GAP2):c.3978G>T (p.Glu1326Asp)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023