NM_016239.4(MYO15A):c.7436A>G (p.Gln2479Arg) 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:
- RCV000293544.5
Allele description [Variation Report for NM_016239.4(MYO15A):c.7436A>G (p.Gln2479Arg)]
NM_016239.4(MYO15A):c.7436A>G (p.Gln2479Arg)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024