Annotation Detail
Information
- Associated Genes
- GJB2
- Associated Variants
-
GJB2 p.Trp44Ter (p.W44*)
(
ENST00000382848.5,
ENST00000382844.2 )
GJB2 p.Trp44Ter (p.W44*) ( ENST00000382844.2, ENST00000382848.5 ) - Associated Disease
- Autosomal recessive nonsyndromic hearing loss 1A
- Source Database
- ClinVar
- Description
- NM_004004.6(GJB2):c.132G>A (p.Trp44Ter) AND Autosomal recessive nonsyndromic hearing loss 1A
- ClinVar Allele ID
- 169013
- ClinVar RefSeq Alternation Syntax
- NM_004004.6:c.132G>A
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-12-24
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000984267
- ClinVar Disease
- Autosomal recessive nonsyndromic hearing loss 1A
- Observed Origin Sample
- germline
- Observed Origin Sample
- inherited
- Observed Origin Sample
- unknown
Drugs