NM_002700.3(POU4F3):c.675A>T (p.Gln225His) AND Autosomal dominant nonsyndromic hearing loss 15
- Germline classification:
- Uncertain significance (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003447390.1
Allele description [Variation Report for NM_002700.3(POU4F3):c.675A>T (p.Gln225His)]
NM_002700.3(POU4F3):c.675A>T (p.Gln225His)
Condition(s)
Assertion and evidence details
Last Updated: Sep 1, 2024