Annotation Detail
Information
- Associated Genes
- IKBKB
- Associated Variants
-
IKBKB c.-18-96A>T
(
ENST00000518983.1,
ENST00000520810.6,
ENST00000520835.7 )
IKBKB c.-18-96A>T ( ENST00000518983.1, ENST00000520810.6, ENST00000520835.7 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_001556.3(IKBKB):c.-18-96A>T AND not specified
- ClinVar Allele ID
- 1256617
- ClinVar RefSeq Alternation Syntax
- NM_001242778.2:c.-100-96A>T
- ClinVar RefSeq Alternation Syntax
- NM_001556.3:c.-18-96A>T
- ClinVar RefSeq Alternation Syntax
- NM_001190720.3:c.-88+518A>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2024-01-24
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003487667
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs