NM_001145809.2(MYH14):c.3883C>T (p.Arg1295Trp) AND Autosomal dominant nonsyndromic hearing loss 4A
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001133312.4
Allele description [Variation Report for NM_001145809.2(MYH14):c.3883C>T (p.Arg1295Trp)]
NM_001145809.2(MYH14):c.3883C>T (p.Arg1295Trp)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024