NM_000466.3(PEX1):c.3588G>A (p.Leu1196=) AND Zellweger spectrum disorders
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 9, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003759906.1
Allele description [Variation Report for NM_000466.3(PEX1):c.3588G>A (p.Leu1196=)]
NM_000466.3(PEX1):c.3588G>A (p.Leu1196=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024