NM_001372044.2(SHANK3):c.3559C>T (p.Leu1187=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 15, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002312773.9
Allele description [Variation Report for NM_001372044.2(SHANK3):c.3559C>T (p.Leu1187=)]
NM_001372044.2(SHANK3):c.3559C>T (p.Leu1187=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 26, 2024