NM_138691.3(TMC1):c.703G>T (p.Ala235Ser) AND Autosomal recessive nonsyndromic hearing loss 7
- 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:
- RCV000316961.5
Allele description [Variation Report for NM_138691.3(TMC1):c.703G>T (p.Ala235Ser)]
NM_138691.3(TMC1):c.703G>T (p.Ala235Ser)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024