NM_005422.4(TECTA):c.2088C>T (p.Cys696=) AND Autosomal recessive nonsyndromic hearing loss 21
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001103457.4
Allele description [Variation Report for NM_005422.4(TECTA):c.2088C>T (p.Cys696=)]
NM_005422.4(TECTA):c.2088C>T (p.Cys696=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024