NM_015346.4(ZFYVE26):c.4260C>T (p.Ser1420=) AND Spastic paraplegia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001444382.7
Allele description [Variation Report for NM_015346.4(ZFYVE26):c.4260C>T (p.Ser1420=)]
NM_015346.4(ZFYVE26):c.4260C>T (p.Ser1420=)
Condition(s)
- Name:
- Spastic paraplegia
- Identifiers:
- MedGen: C0037772; Human Phenotype Ontology: HP:0001258
-
aminopeptidase O isoform X4 [Homo sapiens]
aminopeptidase O isoform X4 [Homo sapiens]gi|2462626909|ref|XP_054220008.1|Protein
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Last Updated: Sep 29, 2024