NM_001171613.2(PREPL):c.1701T>C (p.Tyr567=) AND Myasthenic syndrome, congenital, 22
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 3, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001500380.7
Allele description [Variation Report for NM_001171613.2(PREPL):c.1701T>C (p.Tyr567=)]
NM_001171613.2(PREPL):c.1701T>C (p.Tyr567=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024