NM_145239.3(PRRT2):c.879+5G>A AND Seizures, benign familial infantile, 2
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Jan 13, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000024171.8
Allele description [Variation Report for NM_145239.3(PRRT2):c.879+5G>A]
NM_145239.3(PRRT2):c.879+5G>A
Condition(s)
Assertion and evidence details
Last Updated: Mar 10, 2024