Annotation Detail
Information
- Associated Genes
- VAMP8
- Associated Variants
-
VAMP8 c.*143T>C
(
ENST00000263864.10,
ENST00000409760.1,
ENST00000432071.1 )
VAMP8 c.*143T>C ( ENST00000263864.10, ENST00000409760.1, ENST00000432071.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_003761.5(VAMP8):c.*143T>C AND not provided
- ClinVar Allele ID
- 1171000
- ClinVar RefSeq Alternation Syntax
- NM_003761.5:c.*143T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2020-11-02
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001539917
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs