NM_004565.3(PEX14):c.996T>C (p.Asp332=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 4, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000729648.4
Allele description [Variation Report for NM_004565.3(PEX14):c.996T>C (p.Asp332=)]
NM_004565.3(PEX14):c.996T>C (p.Asp332=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024