NM_001145809.2(MYH14):c.5C>T (p.Ala2Val) AND Nonsyndromic Hearing Loss, Dominant
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 14, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000262635.5
Allele description [Variation Report for NM_001145809.2(MYH14):c.5C>T (p.Ala2Val)]
NM_001145809.2(MYH14):c.5C>T (p.Ala2Val)
Condition(s)
- Name:
- Nonsyndromic Hearing Loss, Dominant
- Identifiers:
- MedGen: CN239435
Assertion and evidence details
Last Updated: Apr 9, 2023