Annotation Detail
Information
- Associated Genes
- SLC2A1
- Associated Variants
-
SLC2A1 p.Asn34Asp (p.N34D)
(
ENST00000426263.10,
ENST00000674765.1 )
SLC2A1 p.Asn34Asp (p.N34D) ( ENST00000426263.10, ENST00000674765.1 ) - Associated Disease
- Encephalopathy due to GLUT1 deficiency
- Source Database
- ClinVar
- Description
- NM_006516.4(SLC2A1):c.100A>G (p.Asn34Asp) AND Encephalopathy due to GLUT1 deficiency
- ClinVar Allele ID
- 167995
- ClinVar RefSeq Alternation Syntax
- NM_006516.4:c.100A>G
- Clinical Significance Description
- Pathogenic/Likely pathogenic
- Clinical Significance Last Update
- 2023-04-11
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000147518
- ClinVar Disease
- Encephalopathy due to GLUT1 deficiency
- Observed Origin Sample
- germline
Drugs