NM_020745.4(AARS2):c.2416C>T (p.Arg806Trp) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 10, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003061779.9
Allele description [Variation Report for NM_020745.4(AARS2):c.2416C>T (p.Arg806Trp)]
NM_020745.4(AARS2):c.2416C>T (p.Arg806Trp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 8, 2024