NM_206933.4(USH2A):c.12667T>C (p.Phe4223Leu) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 16, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000664798.1
Allele description [Variation Report for NM_206933.4(USH2A):c.12667T>C (p.Phe4223Leu)]
NM_206933.4(USH2A):c.12667T>C (p.Phe4223Leu)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024