NM_001128228.3(TPRN):c.1936G>A (p.Glu646Lys) AND Autosomal recessive nonsyndromic hearing loss 79
- Germline classification:
- Uncertain significance (1 submission)
- 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:
- RCV000764825.2
Allele description [Variation Report for NM_001128228.3(TPRN):c.1936G>A (p.Glu646Lys)]
NM_001128228.3(TPRN):c.1936G>A (p.Glu646Lys)
Condition(s)
Assertion and evidence details
Last Updated: Mar 4, 2023