NM_005234.4(NR2F6):c.1084G>A (p.Ala362Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004491276.1
Allele description [Variation Report for NM_005234.4(NR2F6):c.1084G>A (p.Ala362Thr)]
NM_005234.4(NR2F6):c.1084G>A (p.Ala362Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024