NM_001377265.1(MAPT):c.2091T>C (p.Ser697=) AND not provided
- Germline classification:
- not provided (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000084531.2
Allele description [Variation Report for NM_001377265.1(MAPT):c.2091T>C (p.Ser697=)]
NM_001377265.1(MAPT):c.2091T>C (p.Ser697=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024
SCV000116667