Annotation Detail
Information
- Associated Genes
- CDKN1B
- Associated Variants
-
CDKN1B c.-79T>C
(
ENST00000228872.9,
ENST00000614874.2 )
CDKN1B c.-79T>C ( ENST00000228872.9, ENST00000614874.2 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_004064.5(CDKN1B):c.-79T>C AND not provided
- ClinVar Allele ID
- 331119
- ClinVar RefSeq Alternation Syntax
- NM_004064.5:c.-79T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-06-22
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001706463
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs