Variant #0000331088 (NC_000006.11:g.71571383C>T, NM_080742.2:c.955G>A (B3GAT2))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.71571383C>T
DNA change (hg38) g.70861680C>T
Published as B3GAT2(NM_080742.2):c.955G>A (p.(Val319Met))
ISCN -
DB-ID B3GAT2_000001
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) 0.0018 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMAP1 NM_001044305.1 ?/. - c.*1346C>T r.(=) p.(=)
B3GAT2 NM_080742.2 ?/. - c.955G>A r.(?) p.(Val319Met)


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