NM_138691.3(TMC1):c.2144A>T (p.Tyr715Phe) AND Autosomal dominant nonsyndromic hearing loss 36
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001169137.4
Allele description [Variation Report for NM_138691.3(TMC1):c.2144A>T (p.Tyr715Phe)]
NM_138691.3(TMC1):c.2144A>T (p.Tyr715Phe)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023