NM_138691.3(TMC1):c.1608C>T (p.Tyr536=) AND Autosomal dominant nonsyndromic hearing loss 36
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000392367.5
Allele description [Variation Report for NM_138691.3(TMC1):c.1608C>T (p.Tyr536=)]
NM_138691.3(TMC1):c.1608C>T (p.Tyr536=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024