NM_001286577.2(C2CD3):c.6885C>T (p.Leu2295=) AND C2CD3-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003894651.1
Allele description [Variation Report for NM_001286577.2(C2CD3):c.6885C>T (p.Leu2295=)]
NM_001286577.2(C2CD3):c.6885C>T (p.Leu2295=)
Condition(s)
- Name:
- C2CD3-related disorder
- Synonyms:
- C2CD3-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 26, 2024