NM_006772.3(SYNGAP1):c.2627C>T (p.Ser876Leu) AND Intellectual disability, autosomal dominant 5
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003615949.2
Allele description [Variation Report for NM_006772.3(SYNGAP1):c.2627C>T (p.Ser876Leu)]
NM_006772.3(SYNGAP1):c.2627C>T (p.Ser876Leu)
Condition(s)
-
Urinary Diversion
Urinary DiversionTemporary or permanent diversion of the flow of urine through the ureter away from the URINARY BLADDER in the presence of a bladder disease or after cystectomy. There is a var...<br/>MeSH
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Last Updated: Sep 29, 2024