NM_025137.4(SPG11):c.1347C>T (p.Thr449=) AND Hereditary spastic paraplegia
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001847724.4
Allele description [Variation Report for NM_025137.4(SPG11):c.1347C>T (p.Thr449=)]
NM_025137.4(SPG11):c.1347C>T (p.Thr449=)
Condition(s)
-
Homo sapiens L-2-hydroxyglutarate dehydrogenase (L2HGDH), mRNA
Homo sapiens L-2-hydroxyglutarate dehydrogenase (L2HGDH), mRNAgi|13376330|ref|NM_024884.1|Nucleotide
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Last Updated: May 7, 2024