NM_002109.6(HARS1):c.261C>T (p.His87=) AND Usher syndrome type 3B
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 30, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002619528.2
Allele description [Variation Report for NM_002109.6(HARS1):c.261C>T (p.His87=)]
NM_002109.6(HARS1):c.261C>T (p.His87=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 14, 2024