NM_000466.3(PEX1):c.882T>A (p.Pro294=) AND Zellweger spectrum disorders
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003059561.3
Allele description [Variation Report for NM_000466.3(PEX1):c.882T>A (p.Pro294=)]
NM_000466.3(PEX1):c.882T>A (p.Pro294=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024