NM_016239.4(MYO15A):c.6841G>A (p.Asp2281Asn) AND Autosomal recessive nonsyndromic hearing loss 3
- Germline classification:
- Likely pathogenic (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002225019.1
Allele description [Variation Report for NM_016239.4(MYO15A):c.6841G>A (p.Asp2281Asn)]
NM_016239.4(MYO15A):c.6841G>A (p.Asp2281Asn)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023