NM_001377265.1(MAPT):c.39T>C (p.Asp13=) AND Frontotemporal dementia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 30, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003121633.5
Allele description [Variation Report for NM_001377265.1(MAPT):c.39T>C (p.Asp13=)]
NM_001377265.1(MAPT):c.39T>C (p.Asp13=)
Condition(s)
- Name:
- Frontotemporal dementia (FTD)
- Synonyms:
- FRONTOTEMPORAL LOBE DEMENTIA; WILHELMSEN-LYNCH DISEASE; Dementia, frontotemporal, with parkinsonism; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0017276; MedGen: C0338451; Orphanet: 282; OMIM: 600274; Human Phenotype Ontology: HP:0002145
Assertion and evidence details
Last Updated: Feb 20, 2024