NM_001292063.2(OTOG):c.5696C>A (p.Ser1899Tyr) AND Autosomal recessive nonsyndromic hearing loss 18B
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 3, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001333068.1
Allele description [Variation Report for NM_001292063.2(OTOG):c.5696C>A (p.Ser1899Tyr)]
NM_001292063.2(OTOG):c.5696C>A (p.Ser1899Tyr)
Condition(s)
Assertion and evidence details
Last Updated: Apr 23, 2022