NM_207352.4(CYP4V2):c.594T>C (p.Asp198=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002134559.5
Allele description [Variation Report for NM_207352.4(CYP4V2):c.594T>C (p.Asp198=)]
NM_207352.4(CYP4V2):c.594T>C (p.Asp198=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024