NM_016239.4(MYO15A):c.8334C>T (p.Pro2778=) 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:
- RCV001127230.4
Allele description [Variation Report for NM_016239.4(MYO15A):c.8334C>T (p.Pro2778=)]
NM_016239.4(MYO15A):c.8334C>T (p.Pro2778=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024