Annotation Detail
Information
- Associated Genes
- GJB2
- Associated Variants
-
GJB2 p.Ser17Cys (p.S17C)
(
ENST00000382848.5,
ENST00000382844.2 )
GJB2 p.Ser17Cys (p.S17C) ( ENST00000382844.2, ENST00000382848.5 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_004004.6(GJB2):c.50C>G (p.Ser17Cys) AND not specified
- ClinVar Allele ID
- 175767
- ClinVar RefSeq Alternation Syntax
- NM_004004.6:c.50C>G
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2014-06-30
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000156624
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs