Annotation Detail
Information
- Associated Genes
- CCND2 CCND2-AS1
- Associated Variants
-
CCND2 c.-171C>T, ENSG00000285901 c.-171C>T
(
ENST00000675880.1,
ENST00000261254.8 )
CCND2 c.-171C>T, ENSG00000285901 c.-171C>T ( ENST00000261254.8, ENST00000675880.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_001759.4(CCND2):c.-171C>T AND not provided
- ClinVar Allele ID
- 656161
- ClinVar RefSeq Alternation Syntax
- NM_001759.4:c.-171C>T
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-06-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000837873
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs