NM_001292063.2(OTOG):c.1158G>A (p.Ala386=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Aug 3, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000221349.5
Allele description [Variation Report for NM_001292063.2(OTOG):c.1158G>A (p.Ala386=)]
NM_001292063.2(OTOG):c.1158G>A (p.Ala386=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 16, 2024