NM_001384474.1(LOXHD1):c.1476G>T (p.Trp492Cys) AND Autosomal recessive nonsyndromic hearing loss 77
- Germline classification:
- Uncertain significance (4 submissions)
- Last evaluated:
- Oct 31, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000669450.9
Allele description [Variation Report for NM_001384474.1(LOXHD1):c.1476G>T (p.Trp492Cys)]
NM_001384474.1(LOXHD1):c.1476G>T (p.Trp492Cys)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023