Annotation Detail

Information
Associated Genes
GALT
Associated Variants
GALT p.Asn314Asp (p.N314D) ( ENST00000378842.8, ENST00000450095.6 )
GALT p.Asn314Asp (p.N314D) ( ENST00000378842.8, ENST00000450095.6 )
Associated Disease
not specified
Source Database
ClinVar
Description
NM_000155.2(GALT):c.[940A>G;-119_-116delGTCA] AND not specified
ClinVar Allele ID
18652
ClinVar RefSeq Alternation Syntax
NM_000155.4:c.940A>G
ClinVar RefSeq Alternation Syntax
NM_001258332.2:c.613A>G
ClinVar RefSeq Alternation Syntax
NM_000155.4:c.-119_-116delGTCA
Clinical Significance Description
Uncertain significance
Clinical Significance Last Update
2023-04-06
Clinical Significance Review Status
criteria provided, single submitter
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV003230412
ClinVar Disease
not specified
Observed Origin Sample
germline
Drugs