NM_001170629.2(CHD8):c.1157C>A (p.Pro386Gln) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 17, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001758091.2
Allele description [Variation Report for NM_001170629.2(CHD8):c.1157C>A (p.Pro386Gln)]
NM_001170629.2(CHD8):c.1157C>A (p.Pro386Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023