NM_206933.4(USH2A):c.11928G>T (p.Thr3976=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003574074.2
Allele description [Variation Report for NM_206933.4(USH2A):c.11928G>T (p.Thr3976=)]
NM_206933.4(USH2A):c.11928G>T (p.Thr3976=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024