NM_153676.4(USH1C):c.2167C>T (p.Gln723Ter) AND Usher syndrome type 1C
- Germline classification:
- Uncertain significance (2 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000984230.3
Allele description [Variation Report for NM_153676.4(USH1C):c.2167C>T (p.Gln723Ter)]
NM_153676.4(USH1C):c.2167C>T (p.Gln723Ter)
Condition(s)
Assertion and evidence details
Last Updated: Mar 10, 2024