NM_022124.6(CDH23):c.1446C>A (p.Val482=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 11, 2014
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000039102.6
Allele description [Variation Report for NM_022124.6(CDH23):c.1446C>A (p.Val482=)]
NM_022124.6(CDH23):c.1446C>A (p.Val482=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 20, 2024