NM_001077350.3(NPRL3):c.1351+9C>T AND Epilepsy, familial focal, with variable foci 3
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003756077.2
Allele description [Variation Report for NM_001077350.3(NPRL3):c.1351+9C>T]
NM_001077350.3(NPRL3):c.1351+9C>T
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024