NM_016366.3(CABP2):c.482del (p.Phe161fs) AND Autosomal recessive nonsyndromic hearing loss 93
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Oct 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001780706.4
Allele description [Variation Report for NM_016366.3(CABP2):c.482del (p.Phe161fs)]
NM_016366.3(CABP2):c.482del (p.Phe161fs)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024