NM_001614.5(ACTG1):c.445A>G (p.Thr149Ala) AND Autosomal dominant nonsyndromic hearing loss 20
- 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:
- RCV003388615.2
Allele description [Variation Report for NM_001614.5(ACTG1):c.445A>G (p.Thr149Ala)]
NM_001614.5(ACTG1):c.445A>G (p.Thr149Ala)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024