Annotation Detail
Information
- Associated Genes
- CDKN2B CDKN2B-AS1
- Associated Variants
-
CDKN2B c.*2619C>T
(
ENST00000276925.7 )
CDKN2B c.*2619C>T ( ENST00000276925.7 ) - Source Database
- ClinVar
- Description
- NM_004936.4(CDKN2B):c.*2619C>T AND Malignant tumor of breast
- ClinVar Allele ID
- 800881
- ClinVar RefSeq Alternation Syntax
- NM_078487.2:c.*2922C>T
- ClinVar RefSeq Alternation Syntax
- NM_004936.4:c.*2619C>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2023-07-01
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003447314
- Observed Origin Sample
- somatic
Drugs