NM_133261.3(GIPC3):c.57G>T (p.Ala19=) AND Autosomal recessive nonsyndromic hearing loss 15
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 6, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002500932.1
Allele description [Variation Report for NM_133261.3(GIPC3):c.57G>T (p.Ala19=)]
NM_133261.3(GIPC3):c.57G>T (p.Ala19=)
Condition(s)
Assertion and evidence details
Last Updated: Aug 4, 2024