NM_005422.4(TECTA):c.1089G>T (p.Val363=) AND Autosomal dominant nonsyndromic hearing loss 12
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001103379.4
Allele description [Variation Report for NM_005422.4(TECTA):c.1089G>T (p.Val363=)]
NM_005422.4(TECTA):c.1089G>T (p.Val363=)
Condition(s)
Assertion and evidence details
Last Updated: Apr 9, 2023