NM_014363.6(SACS):c.5841C>T (p.Pro1947=) AND Spastic paraplegia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 27, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001081266.8
Allele description [Variation Report for NM_014363.6(SACS):c.5841C>T (p.Pro1947=)]
NM_014363.6(SACS):c.5841C>T (p.Pro1947=)
Condition(s)
- Name:
- Spastic paraplegia
- Identifiers:
- MedGen: C0037772; Human Phenotype Ontology: HP:0001258
-
Fam136a family with sequence similarity 136, member A [Rattus norvegicus]
Fam136a family with sequence similarity 136, member A [Rattus norvegicus]Gene ID:297415Gene
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Last Updated: Sep 29, 2024