NM_000466.3(PEX1):c.3378C>T (p.Tyr1126=) AND Zellweger spectrum disorders
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 26, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002080501.6
Allele description [Variation Report for NM_000466.3(PEX1):c.3378C>T (p.Tyr1126=)]
NM_000466.3(PEX1):c.3378C>T (p.Tyr1126=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024