NM_001379180.1(ESRRB):c.1119C>T (p.Ser373=) AND Autosomal recessive nonsyndromic hearing loss 35
- 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:
- RCV001120582.4
Allele description [Variation Report for NM_001379180.1(ESRRB):c.1119C>T (p.Ser373=)]
NM_001379180.1(ESRRB):c.1119C>T (p.Ser373=)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023