NM_000288.4(PEX7):c.783C>T (p.Cys261=) AND Peroxisome biogenesis disorder 9B
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003649489.2
Allele description [Variation Report for NM_000288.4(PEX7):c.783C>T (p.Cys261=)]
NM_000288.4(PEX7):c.783C>T (p.Cys261=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024