Annotation Detail
Information
- Associated Genes
- CDKN1B
- Associated Variants
-
CDKN1B p.Val109Ala (p.V109A)
(
ENST00000396340.1,
ENST00000614874.2,
ENST00000228872.9 )
CDKN1B p.Val109Ala (p.V109A) ( ENST00000228872.9, ENST00000396340.1, ENST00000614874.2 ) - Associated Disease
- Hereditary cancer-predisposing syndrome
- Source Database
- ClinVar
- Description
- NM_004064.5(CDKN1B):c.326T>C (p.Val109Ala) AND Hereditary cancer-predisposing syndrome
- ClinVar Allele ID
- 926487
- ClinVar RefSeq Alternation Syntax
- NM_004064.5:c.326T>C
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2024-02-23
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV004032337
- ClinVar Disease
- Hereditary cancer-predisposing syndrome
- Observed Origin Sample
- germline
Drugs