NM_001614.5(ACTG1):c.20C>T (p.Ala7Val) AND Autosomal dominant nonsyndromic hearing loss 20
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Nov 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003886624.1
Allele description [Variation Report for NM_001614.5(ACTG1):c.20C>T (p.Ala7Val)]
NM_001614.5(ACTG1):c.20C>T (p.Ala7Val)
Condition(s)
Assertion and evidence details
Last Updated: Jun 9, 2024