NM_080680.3(COL11A2):c.3059G>A (p.Arg1020Gln) AND Autosomal dominant nonsyndromic hearing loss 13
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002282679.1
Allele description [Variation Report for NM_080680.3(COL11A2):c.3059G>A (p.Arg1020Gln)]
NM_080680.3(COL11A2):c.3059G>A (p.Arg1020Gln)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024