NM_153676.4(USH1C):c.2312G>T (p.Gly771Val) AND Usher syndrome type 1C
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 4, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001830140.1
Allele description [Variation Report for NM_153676.4(USH1C):c.2312G>T (p.Gly771Val)]
NM_153676.4(USH1C):c.2312G>T (p.Gly771Val)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2023