NM_002109.6(HARS1):c.679T>G (p.Ser227Ala) AND Usher syndrome type 3B
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000699134.8
Allele description [Variation Report for NM_002109.6(HARS1):c.679T>G (p.Ser227Ala)]
NM_002109.6(HARS1):c.679T>G (p.Ser227Ala)
Condition(s)
Assertion and evidence details
Last Updated: Jun 9, 2024