NM_001039141.3(TRIOBP):c.964G>T (p.Ala322Ser) AND Autosomal recessive nonsyndromic hearing loss 28
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 7, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001337110.1
Allele description [Variation Report for NM_001039141.3(TRIOBP):c.964G>T (p.Ala322Ser)]
NM_001039141.3(TRIOBP):c.964G>T (p.Ala322Ser)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024