NM_001321142.2(CIDEC):c.387C>G (p.Ser129=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 3, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000890681.3
Allele description [Variation Report for NM_001321142.2(CIDEC):c.387C>G (p.Ser129=)]
NM_001321142.2(CIDEC):c.387C>G (p.Ser129=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023