NM_001377265.1(MAPT):c.13C>T (p.Arg5Cys) AND MAPT-Related Spectrum Disorders
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001123790.5
Allele description [Variation Report for NM_001377265.1(MAPT):c.13C>T (p.Arg5Cys)]
NM_001377265.1(MAPT):c.13C>T (p.Arg5Cys)
Condition(s)
- Name:
- MAPT-Related Spectrum Disorders
- Identifiers:
- MedGen: CN239327
Assertion and evidence details
Last Updated: Feb 20, 2024