NM_000260.4(MYO7A):c.3638G>A (p.Arg1213Gln) AND Autosomal recessive nonsyndromic hearing loss 2
- 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:
- RCV001111014.4
Allele description [Variation Report for NM_000260.4(MYO7A):c.3638G>A (p.Arg1213Gln)]
NM_000260.4(MYO7A):c.3638G>A (p.Arg1213Gln)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024