NM_001292063.2(OTOG):c.6012C>T (p.Asp2004=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 23, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001195584.4
Allele description [Variation Report for NM_001292063.2(OTOG):c.6012C>T (p.Asp2004=)]
NM_001292063.2(OTOG):c.6012C>T (p.Asp2004=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 20, 2024