NM_001145809.2(MYH14):c.5041G>A (p.Glu1681Lys) AND Autosomal dominant nonsyndromic hearing loss 4A
- Germline classification:
- Likely benign (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:
- RCV000269098.5
Allele description [Variation Report for NM_001145809.2(MYH14):c.5041G>A (p.Glu1681Lys)]
NM_001145809.2(MYH14):c.5041G>A (p.Glu1681Lys)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023