Annotation Detail
Information
- Associated Genes
- NFKBIA
- Associated Variants
-
NFKBIA c.*126G>A
(
ENST00000557140.5,
ENST00000697961.1,
ENST00000557389.1,
ENST00000216797.10 )
NFKBIA c.*126G>A ( ENST00000216797.10, ENST00000557140.5, ENST00000557389.1, ENST00000697961.1 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_020529.3(NFKBIA):c.*126G>A AND not specified
- ClinVar Allele ID
- 337761
- ClinVar RefSeq Alternation Syntax
- NM_020529.3:c.*126G>A
- 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/RCV003488527
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs