NM_182548.4(LHFPL5):c.411G>T (p.Ala137=) AND Autosomal recessive nonsyndromic hearing loss 67
- 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:
- RCV001153870.4
Allele description [Variation Report for NM_182548.4(LHFPL5):c.411G>T (p.Ala137=)]
NM_182548.4(LHFPL5):c.411G>T (p.Ala137=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023