NM_138691.3(TMC1):c.545G>T (p.Gly182Val) AND Autosomal recessive nonsyndromic hearing loss 7
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001808043.1
Allele description [Variation Report for NM_138691.3(TMC1):c.545G>T (p.Gly182Val)]
NM_138691.3(TMC1):c.545G>T (p.Gly182Val)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023