NM_003907.3(EIF2B5):c.870C>T (p.His290=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000930175.6
Allele description [Variation Report for NM_003907.3(EIF2B5):c.870C>T (p.His290=)]
NM_003907.3(EIF2B5):c.870C>T (p.His290=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024