NM_022124.6(CDH23):c.5931T>C (p.Pro1977=) AND Autosomal recessive nonsyndromic hearing loss 12
- 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:
- RCV000373401.5
Allele description [Variation Report for NM_022124.6(CDH23):c.5931T>C (p.Pro1977=)]
NM_022124.6(CDH23):c.5931T>C (p.Pro1977=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024