NM_206933.4(USH2A):c.2137G>C (p.Gly713Arg) AND not provided
- Germline classification:
- Benign (5 submissions)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000087010.25
Allele description [Variation Report for NM_206933.4(USH2A):c.2137G>C (p.Gly713Arg)]
NM_206933.4(USH2A):c.2137G>C (p.Gly713Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024