NM_001414.4(EIF2B1):c.786T>C (p.Thr262=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 14, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003843680.2
Allele description [Variation Report for NM_001414.4(EIF2B1):c.786T>C (p.Thr262=)]
NM_001414.4(EIF2B1):c.786T>C (p.Thr262=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Sep 29, 2024