NM_014874.4(MFN2):c.193G>T (p.Glu65Ter) AND Charcot-Marie-Tooth disease
- Germline classification:
- Uncertain significance (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000790046.1
Allele description [Variation Report for NM_014874.4(MFN2):c.193G>T (p.Glu65Ter)]
NM_014874.4(MFN2):c.193G>T (p.Glu65Ter)
Condition(s)
Assertion and evidence details
Last Updated: Apr 23, 2022