Annotation Detail

Information
Associated Genes
GALT
Associated Variants
GALT p.Leu195Pro (p.L195P) ( ENST00000378842.8, ENST00000450095.6 )
GALT p.Leu195Pro (p.L195P) ( ENST00000378842.8, ENST00000450095.6 )
Associated Disease
not provided
Source Database
ClinVar
Description
NM_000155.4(GALT):c.584T>C (p.Leu195Pro) AND not provided
ClinVar Allele ID
36556
ClinVar RefSeq Alternation Syntax
NM_000155.4:c.584T>C
ClinVar RefSeq Alternation Syntax
NM_001258332.2:c.257T>C
Clinical Significance Description
Pathogenic
Clinical Significance Last Update
2023-06-01
Clinical Significance Review Status
criteria provided, multiple submitters, no conflicts
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000224416
ClinVar Disease
not provided
Observed Origin Sample
germline
Drugs