Variant #0000613577 (NC_000011.9:g.66114375A>G, NM_006876.2:c.642T>C (B3GNT1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66114375A>G
DNA change (hg38) g.66346904A>G
Published as B4GAT1(NM_006876.2):c.642T>C (p.N214=)
ISCN -
DB-ID B3GNT1_000009
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-30 18:25:35 +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 -?/. - c.642T>C r.(?) p.(Asn214=)
BRMS1 NM_015399.3 -?/. - c.-1940T>C r.(?) p.(=)


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