Annotation Detail
Information
- Associated Genes
- GJB2
- Associated Variants
-
GJB2 p.Ile82Met (p.I82M)
(
ENST00000382844.2,
ENST00000382848.5 )
GJB2 p.Ile82Met (p.I82M) ( ENST00000382844.2, ENST00000382848.5 ) - Associated Disease
- GJB2-related disorder
- Source Database
- ClinVar
- Description
- NM_004004.6(GJB2):c.246C>G (p.Ile82Met) AND GJB2-related disorder
- ClinVar Allele ID
- 186859
- ClinVar RefSeq Alternation Syntax
- NM_004004.6:c.246C>G
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2023-09-21
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004528922
- ClinVar Disease
- GJB2-related disorder
- Observed Origin Sample
- germline
Drugs