NM_206933.4(USH2A):c.2196A>G (p.Gly732=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001495418.6
Allele description [Variation Report for NM_206933.4(USH2A):c.2196A>G (p.Gly732=)]
NM_206933.4(USH2A):c.2196A>G (p.Gly732=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024