Annotation Detail
Information
- Associated Genes
- SLC2A1
- Associated Variants
-
SLC2A1 p.Lys7_Thr9del (p.K7_T9del)
(
ENST00000426263.10,
ENST00000674765.1 )
SLC2A1 p.Lys7_Thr9del (p.K7_T9del) ( ENST00000426263.10, ENST00000674765.1 ) - Associated Disease
- Encephalopathy due to GLUT1 deficiency
- Source Database
- ClinVar
- Description
- NM_006516.2(SLC2A1):c.19_28delAAGCTGACGG (p.Lys7Valfs) AND Encephalopathy due to GLUT1 deficiency
- ClinVar Allele ID
- 167996
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2013-02-08
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000147524
- ClinVar Disease
- Encephalopathy due to GLUT1 deficiency
- Observed Origin Sample
- germline
Drugs