NM_020631.6(PLEKHG5):c.411G>T (p.Arg137Ser) AND Charcot-Marie-Tooth disease recessive intermediate C
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 27, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001329767.1
Allele description [Variation Report for NM_020631.6(PLEKHG5):c.411G>T (p.Arg137Ser)]
NM_020631.6(PLEKHG5):c.411G>T (p.Arg137Ser)
Condition(s)
Assertion and evidence details
Last Updated: Jan 26, 2024