NM_005523.6(HOXA11):c.679G>C (p.Gly227Arg) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002481212.3
Allele description [Variation Report for NM_005523.6(HOXA11):c.679G>C (p.Gly227Arg)]
NM_005523.6(HOXA11):c.679G>C (p.Gly227Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jul 7, 2024