NM_005654.6(NR2F1):c.114C>A (p.Gly38=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002608945.2
Allele description [Variation Report for NM_005654.6(NR2F1):c.114C>A (p.Gly38=)]
NM_005654.6(NR2F1):c.114C>A (p.Gly38=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024