NM_000466.3(PEX1):c.2901G>A (p.Gln967=) AND Zellweger spectrum disorders
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001507152.8
Allele description [Variation Report for NM_000466.3(PEX1):c.2901G>A (p.Gln967=)]
NM_000466.3(PEX1):c.2901G>A (p.Gln967=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 10, 2024