NM_206933.4(USH2A):c.3177G>A (p.Pro1059=) AND Usher syndrome type 2A
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000383428.5
Allele description [Variation Report for NM_206933.4(USH2A):c.3177G>A (p.Pro1059=)]
NM_206933.4(USH2A):c.3177G>A (p.Pro1059=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024