NM_000260.4(MYO7A):c.813C>T (p.Gly271=) AND Autosomal dominant nonsyndromic hearing loss 11
- Germline classification:
- Likely benign (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:
- RCV001113654.4
Allele description [Variation Report for NM_000260.4(MYO7A):c.813C>T (p.Gly271=)]
NM_000260.4(MYO7A):c.813C>T (p.Gly271=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024