NM_003907.3(EIF2B5):c.514C>A (p.Arg172=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003702524.1
Allele description [Variation Report for NM_003907.3(EIF2B5):c.514C>A (p.Arg172=)]
NM_003907.3(EIF2B5):c.514C>A (p.Arg172=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024