NM_024306.5(FA2H):c.266A>T (p.Gln89Leu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003117764.3
Allele description [Variation Report for NM_024306.5(FA2H):c.266A>T (p.Gln89Leu)]
NM_024306.5(FA2H):c.266A>T (p.Gln89Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Nov 11, 2023