NM_206933.4(USH2A):c.8778G>T (p.Glu2926Asp) AND Usher syndrome type 2A
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001273710.1
Allele description [Variation Report for NM_206933.4(USH2A):c.8778G>T (p.Glu2926Asp)]
NM_206933.4(USH2A):c.8778G>T (p.Glu2926Asp)
Condition(s)
Assertion and evidence details
Last Updated: Mar 4, 2023