NM_001034116.2(EIF2B4):c.1476T>G (p.Thr492=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003570779.2
Allele description [Variation Report for NM_001034116.2(EIF2B4):c.1476T>G (p.Thr492=)]
NM_001034116.2(EIF2B4):c.1476T>G (p.Thr492=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024