NM_000466.3(PEX1):c.939T>C (p.His313=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 15, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000296594.6
Allele description [Variation Report for NM_000466.3(PEX1):c.939T>C (p.His313=)]
NM_000466.3(PEX1):c.939T>C (p.His313=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024