NM_177398.4(LMX1A):c.1050T>C (p.Asp350=) AND Autosomal dominant nonsyndromic hearing loss 7
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Aug 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001730996.2
Allele description [Variation Report for NM_177398.4(LMX1A):c.1050T>C (p.Asp350=)]
NM_177398.4(LMX1A):c.1050T>C (p.Asp350=)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023