NM_001292063.2(OTOG):c.441C>T (p.His147=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jul 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000933962.7
Allele description [Variation Report for NM_001292063.2(OTOG):c.441C>T (p.His147=)]
NM_001292063.2(OTOG):c.441C>T (p.His147=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024