NM_000260.4(MYO7A):c.1543A>C (p.Lys515Gln) AND Autosomal recessive nonsyndromic hearing loss 2
- 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:
- RCV001110522.4
Allele description [Variation Report for NM_000260.4(MYO7A):c.1543A>C (p.Lys515Gln)]
NM_000260.4(MYO7A):c.1543A>C (p.Lys515Gln)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024