NM_153676.4(USH1C):c.1592G>A (p.Arg531His) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 6, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000930840.3
Allele description [Variation Report for NM_153676.4(USH1C):c.1592G>A (p.Arg531His)]
NM_153676.4(USH1C):c.1592G>A (p.Arg531His)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Sep 17, 2022