Annotation Detail
Information
- Associated Genes
- GALT
- Associated Variants
-
GALT p.Arg333Trp (p.R333W)
(
ENST00000378842.8,
ENST00000450095.6 )
GALT p.Arg333Trp (p.R333W) ( ENST00000378842.8, ENST00000450095.6 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000155.4(GALT):c.997C>T (p.Arg333Trp) AND not provided
- ClinVar Allele ID
- 18649
- ClinVar RefSeq Alternation Syntax
- NM_000155.4:c.997C>T
- ClinVar RefSeq Alternation Syntax
- NM_001258332.2:c.670C>T
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2021-08-05
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000723400
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs