NM_033517.1(SHANK3):c.3013C>G (p.Pro1005Ala) AND History of neurodevelopmental disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 22, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000717607.1
Allele description
NM_033517.1(SHANK3):c.3013C>G (p.Pro1005Ala)
Condition(s)
- Name:
- History of neurodevelopmental disorder
- Identifiers:
- MedGen: C2711754
Assertion and evidence details
Last Updated: Apr 23, 2022