NM_206933.4(USH2A):c.10851C>T (p.Asn3617=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000964832.16
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)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 1, 2024