Annotation Detail
Information
- Associated Genes
- SLC2A1
- Associated Variants
-
SLC2A1 p.Arg92= (p.R92=)
(
ENST00000674765.1,
ENST00000426263.10 )
SLC2A1 p.Arg92= (p.R92=) ( ENST00000426263.10, ENST00000674765.1 ) - Associated Disease
- Encephalopathy due to GLUT1 deficiency
- Source Database
- ClinVar
- Description
- NM_006516.4(SLC2A1):c.274C>A (p.Arg92=) AND Encephalopathy due to GLUT1 deficiency
- ClinVar Allele ID
- 201165
- ClinVar RefSeq Alternation Syntax
- NM_006516.4:c.274C>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-03-06
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000722005
- ClinVar Disease
- Encephalopathy due to GLUT1 deficiency
- Observed Origin Sample
- germline
Drugs