Annotation Detail

Information
Associated Genes
GALT
Associated Variants
GALT p.Tyr209Cys (p.Y209C) ( ENST00000378842.8, ENST00000450095.6 )
GALT p.Tyr209Cys (p.Y209C) ( ENST00000378842.8, ENST00000450095.6 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_000155.4(GALT):c.626A>G (p.Tyr209Cys) AND not provided
ClinVar Allele ID
36565
ClinVar RefSeq Alternation Syntax
NM_001258332.2:c.299A>G
ClinVar RefSeq Alternation Syntax
NM_000155.4:c.626A>G
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2022-02-28
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000185918
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs