Annotation Detail
Information
- Associated Genes
- AMPD1
- Associated Variants
-
AMPD1 p.Gln12Ter (p.Q12*)
(
ENST00000369538.4,
ENST00000520113.7 )
AMPD1 p.Gln12Ter (p.Q12*) ( ENST00000369538.4, ENST00000520113.7 ) - Associated Disease
- AMPD1-related disorder
- Source Database
- ClinVar
- Description
- NM_000036.3(AMPD1):c.34C>T (p.Gln12Ter) AND AMPD1-related disorder
- ClinVar Allele ID
- 33310
- ClinVar RefSeq Alternation Syntax
- NM_000036.3:c.34C>T
- ClinVar RefSeq Alternation Syntax
- NM_001172626.2:c.22+2014C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2023-12-01
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003974848
- ClinVar Disease
- AMPD1-related disorder
- Observed Origin Sample
- germline
Drugs