NM_001393500.2(TOMT):c.110G>A (p.Arg37Gln) AND Autosomal recessive nonsyndromic hearing loss 63
- 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:
- RCV000361489.5
Allele description [Variation Report for NM_001393500.2(TOMT):c.110G>A (p.Arg37Gln)]
NM_001393500.2(TOMT):c.110G>A (p.Arg37Gln)
Condition(s)
Assertion and evidence details
Last Updated: Sep 1, 2024