Variant #0000245364 (NC_000011.9:g.66113600T>C, NM_006876.2:c.1168A>G (B3GNT1))

Chromosome 11
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.66113600T>C
DNA change (hg38) g.66346129T>C
Published as -
ISCN -
DB-ID B3GNT1_000001 See all 5 reported entries
Variant remarks expression cloning; normal cellular localisation, significantly decreased glycosyltransferase function
Reference PubMed: Buysse 2013
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-04-02 19:24:38 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B3GNT1 NM_006876.2 +/. 1 c.1168A>G r.(?) p.Asn390Asp


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