Annotation Detail
Information
- Associated Genes
- GJB2
- Associated Variants
-
GJB2 p.Tyr65Cys (p.Y65C)
(
ENST00000382848.5,
ENST00000382844.2 )
GJB2 p.Tyr65Cys (p.Y65C) ( ENST00000382844.2, ENST00000382848.5 ) - Associated Disease
- Autosomal recessive nonsyndromic hearing loss 1A
- Source Database
- ClinVar
- Description
- NM_004004.6(GJB2):c.194A>G (p.Tyr65Cys) AND Autosomal recessive nonsyndromic hearing loss 1A
- ClinVar Allele ID
- 53894
- ClinVar RefSeq Alternation Syntax
- NM_004004.6:c.194A>G
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2023-06-02
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001826561
- ClinVar Disease
- Autosomal recessive nonsyndromic hearing loss 1A
- Observed Origin Sample
- germline
Drugs