NM_032251.6(CCDC88B):c.2792C>T (p.Ala931Val) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004430370.1
Allele description [Variation Report for NM_032251.6(CCDC88B):c.2792C>T (p.Ala931Val)]
NM_032251.6(CCDC88B):c.2792C>T (p.Ala931Val)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024