NM_000399.5(EGR2):c.1277G>A (p.Arg426Gln) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001843536.2
Allele description [Variation Report for NM_000399.5(EGR2):c.1277G>A (p.Arg426Gln)]
NM_000399.5(EGR2):c.1277G>A (p.Arg426Gln)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024