NM_001372044.2(SHANK3):c.3133G>T (p.Ala1045Ser) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Aug 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001711795.15
Allele description [Variation Report for NM_001372044.2(SHANK3):c.3133G>T (p.Ala1045Ser)]
NM_001372044.2(SHANK3):c.3133G>T (p.Ala1045Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jul 7, 2024