NM_153676.4(USH1C):c.567G>T (p.Val189=) AND Usher syndrome type 1C
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 11, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001280399.1
Allele description [Variation Report for NM_153676.4(USH1C):c.567G>T (p.Val189=)]
NM_153676.4(USH1C):c.567G>T (p.Val189=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024