NM_016239.4(MYO15A):c.6337A>T (p.Ile2113Phe) AND Nonsyndromic genetic hearing loss
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Sep 28, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002228014.1
Allele description [Variation Report for NM_016239.4(MYO15A):c.6337A>T (p.Ile2113Phe)]
NM_016239.4(MYO15A):c.6337A>T (p.Ile2113Phe)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024