NM_016239.4(MYO15A):c.6559C>T (p.Arg2187Cys) AND Autosomal recessive nonsyndromic hearing loss 3
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000358118.5
Allele description [Variation Report for NM_016239.4(MYO15A):c.6559C>T (p.Arg2187Cys)]
NM_016239.4(MYO15A):c.6559C>T (p.Arg2187Cys)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023