NM_207352.4(CYP4V2):c.775C>A (p.Gln259Lys) AND not specified
- Germline classification:
- Benign (3 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000244699.9
Allele description [Variation Report for NM_207352.4(CYP4V2):c.775C>A (p.Gln259Lys)]
NM_207352.4(CYP4V2):c.775C>A (p.Gln259Lys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 16, 2024