NM_016239.4(MYO15A):c.3774C>T (p.Ile1258=) AND Autosomal recessive nonsyndromic hearing loss 3
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000263636.6
Allele description [Variation Report for NM_016239.4(MYO15A):c.3774C>T (p.Ile1258=)]
NM_016239.4(MYO15A):c.3774C>T (p.Ile1258=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 20, 2024