Variant #0000621742 (NC_000006.11:g.71508417G>A, NM_080742.2:c.*62949C>T (B3GAT2))

Chromosome 6
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.71508417G>A
DNA change (hg38) g.70798714G>A
Published as SMAP1(NM_001281439.1):c.472G>A (p.A158T)
ISCN -
DB-ID B3GAT2_000005
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 2019-12-06 12:43:26 +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.553G>A r.(?) p.(Ala185Thr)
B3GAT2 NM_080742.2 -?/. - c.*62949C>T r.(=) p.(=)


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