NM_001256317.3(TMPRSS3):c.411C>T (p.Tyr137=) AND Autosomal recessive nonsyndromic hearing loss 8
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001140694.4
Allele description [Variation Report for NM_001256317.3(TMPRSS3):c.411C>T (p.Tyr137=)]
NM_001256317.3(TMPRSS3):c.411C>T (p.Tyr137=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024