NM_005654.6(NR2F1):c.40G>T (p.Asp14Tyr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004028298.1
Allele description [Variation Report for NM_005654.6(NR2F1):c.40G>T (p.Asp14Tyr)]
NM_005654.6(NR2F1):c.40G>T (p.Asp14Tyr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 7, 2024