NM_000522.5(HOXA13):c.527G>A (p.Ser176Asn) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002496096.1
Allele description [Variation Report for NM_000522.5(HOXA13):c.527G>A (p.Ser176Asn)]
NM_000522.5(HOXA13):c.527G>A (p.Ser176Asn)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023