NM_002109.6(HARS1):c.423G>T (p.Met141Ile) AND Usher syndrome type 3B
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003076382.2
Allele description [Variation Report for NM_002109.6(HARS1):c.423G>T (p.Met141Ile)]
NM_002109.6(HARS1):c.423G>T (p.Met141Ile)
Condition(s)
Assertion and evidence details
Last Updated: Feb 14, 2024