NM_014946.4(SPAST):c.1206C>T (p.Thr402=) AND Hereditary spastic paraplegia 4
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002690621.2
Allele description [Variation Report for NM_014946.4(SPAST):c.1206C>T (p.Thr402=)]
NM_014946.4(SPAST):c.1206C>T (p.Thr402=)
Condition(s)
-
Same, Connectivity for PubChem Compound (Select 70229199) (1)
PubChem Compound
-
Same Parent, Stereochemistry for PubChem Compound (Select 7022919... (1)
Same Parent, Stereochemistry for PubChem Compound (Select 70229199)SearchPubChem Compound
-
PubChem Same Substances for PubChem Compound (Select 70229199) (4)
PubChem Substance
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Last Updated: Feb 28, 2024