NM_001292063.2(OTOG):c.397G>A (p.Gly133Ser) AND Hearing impairment
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001375221.3
Allele description [Variation Report for NM_001292063.2(OTOG):c.397G>A (p.Gly133Ser)]
NM_001292063.2(OTOG):c.397G>A (p.Gly133Ser)
Condition(s)
- Name:
- Hearing impairment
- Identifiers:
- MONDO: MONDO:0005365; MedGen: C1384666; Human Phenotype Ontology: HP:0000365
-
tlk2 tousled-like kinase 2 [Danio rerio]
tlk2 tousled-like kinase 2 [Danio rerio]Gene ID:407732Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Aug 4, 2024