NM_001042702.5(PJVK):c.405A>C (p.Thr135=) AND Autosomal recessive nonsyndromic hearing loss 59
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001133847.4
Allele description [Variation Report for NM_001042702.5(PJVK):c.405A>C (p.Thr135=)]
NM_001042702.5(PJVK):c.405A>C (p.Thr135=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024