NM_206933.4(USH2A):c.10851C>T (p.Asn3617=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002504921.8
Allele description [Variation Report for NM_206933.4(USH2A):c.10851C>T (p.Asn3617=)]
NM_206933.4(USH2A):c.10851C>T (p.Asn3617=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024