NM_001136023.3(NFE2):c.432C>T (p.Ser144=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003391867.8
Allele description [Variation Report for NM_001136023.3(NFE2):c.432C>T (p.Ser144=)]
NM_001136023.3(NFE2):c.432C>T (p.Ser144=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024