NM_000522.5(HOXA13):c.527G>A (p.Ser176Asn) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 30, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001770868.2
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)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023