NM_001039141.3(TRIOBP):c.4910C>G (p.Thr1637Ser) AND Autosomal recessive nonsyndromic hearing loss 28
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002477864.1
Allele description [Variation Report for NM_001039141.3(TRIOBP):c.4910C>G (p.Thr1637Ser)]
NM_001039141.3(TRIOBP):c.4910C>G (p.Thr1637Ser)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023