NM_032251.6(CCDC88B):c.1536C>A (p.Asp512Glu) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 4, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004430362.1
Allele description [Variation Report for NM_032251.6(CCDC88B):c.1536C>A (p.Asp512Glu)]
NM_032251.6(CCDC88B):c.1536C>A (p.Asp512Glu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024