Annotation Detail
Information
- Associated Genes
- GALT
- Associated Variants
-
GALT p.Gln188Arg (p.Q188R)
(
ENST00000378842.8,
ENST00000450095.6 )
GALT p.Gln188Arg (p.Q188R) ( ENST00000378842.8, ENST00000450095.6 ) - Associated Disease
- GALT-related disorder
- Source Database
- ClinVar
- Description
- NM_000155.4(GALT):c.563A>G (p.Gln188Arg) AND GALT-related disorder
- ClinVar Allele ID
- 18653
- ClinVar RefSeq Alternation Syntax
- NM_001258332.2:c.236A>G
- ClinVar RefSeq Alternation Syntax
- NM_000155.4:c.563A>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2023-08-31
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003415643
- ClinVar Disease
- GALT-related disorder
- Observed Origin Sample
- germline
Drugs