Annotation Detail
Information
- Associated Genes
- SLC2A1
- Associated Variants
-
SLC2A1 p.Tyr432= (p.Y432=)
(
ENST00000674765.1,
ENST00000426263.10 )
SLC2A1 p.Tyr432= (p.Y432=) ( ENST00000426263.10, ENST00000674765.1 ) - Associated Disease
- Inborn genetic diseases
- Source Database
- ClinVar
- Description
- NM_006516.4(SLC2A1):c.1296C>T (p.Tyr432=) AND Inborn genetic diseases
- ClinVar Allele ID
- 101307
- ClinVar RefSeq Alternation Syntax
- NM_006516.4:c.1296C>T
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2017-02-23
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002313781
- ClinVar Disease
- Inborn genetic diseases
- Observed Origin Sample
- germline
Drugs