Annotation Detail
Information
- Associated Genes
- GJB2
- Associated Variants
-
GJB2 p.Lys15Thr (p.K15T)
(
ENST00000382844.2,
ENST00000382848.5 )
GJB2 p.Lys15Thr (p.K15T) ( ENST00000382844.2, ENST00000382848.5 ) - Associated Disease
- Rare genetic deafness
- Source Database
- ClinVar
- Description
- NM_004004.6(GJB2):c.44A>C (p.Lys15Thr) AND Rare genetic deafness
- ClinVar Allele ID
- 53919
- ClinVar RefSeq Alternation Syntax
- NM_004004.6:c.44A>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2020-10-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000211780
- ClinVar Disease
- Rare genetic deafness
- Observed Origin Sample
- germline
Drugs