NM_001292063.2(OTOG):c.6354G>C (p.Leu2118=) AND OTOG-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 7, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003909781.2
Allele description [Variation Report for NM_001292063.2(OTOG):c.6354G>C (p.Leu2118=)]
NM_001292063.2(OTOG):c.6354G>C (p.Leu2118=)
Condition(s)
- Name:
- OTOG-related disorder
- Synonyms:
- OTOG-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Oct 8, 2024