NM_006164.5(NFE2L2):c.1716T>C (p.Asp572=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003429384.10
Allele description [Variation Report for NM_006164.5(NFE2L2):c.1716T>C (p.Asp572=)]
NM_006164.5(NFE2L2):c.1716T>C (p.Asp572=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 20, 2024