Annotation Detail
Information
- Associated Genes
- GJB2
- Associated Variants
-
GJB2 p.His100Tyr (p.H100Y)
(
ENST00000382848.5,
ENST00000382844.2 )
GJB2 p.His100Tyr (p.H100Y) ( ENST00000382844.2, ENST00000382848.5 ) - Associated Disease
- Rare genetic deafness
- Source Database
- ClinVar
- Description
- NM_004004.6(GJB2):c.298C>T (p.His100Tyr) AND Rare genetic deafness
- ClinVar Allele ID
- 169011
- ClinVar RefSeq Alternation Syntax
- NM_004004.6:c.298C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2016-03-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000215444
- ClinVar Disease
- Rare genetic deafness
- Observed Origin Sample
- germline
Drugs