NM_002109.6(HARS1):c.963C>T (p.Asp321=) AND Usher syndrome type 3B
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 21, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001410620.6
Allele description [Variation Report for NM_002109.6(HARS1):c.963C>T (p.Asp321=)]
NM_002109.6(HARS1):c.963C>T (p.Asp321=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024