NM_000260.4(MYO7A):c.2035G>A (p.Val679Ile) AND Autosomal dominant nonsyndromic hearing loss 11
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000320261.13
Allele description [Variation Report for NM_000260.4(MYO7A):c.2035G>A (p.Val679Ile)]
NM_000260.4(MYO7A):c.2035G>A (p.Val679Ile)
Condition(s)
Assertion and evidence details
Last Updated: Oct 26, 2024