NM_015466.4(PTPN23):c.3484C>T (p.Arg1162Trp) AND Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003492739.2
Allele description [Variation Report for NM_015466.4(PTPN23):c.3484C>T (p.Arg1162Trp)]
NM_015466.4(PTPN23):c.3484C>T (p.Arg1162Trp)
Condition(s)
Assertion and evidence details
Last Updated: May 19, 2024