Variant #0000544765 (NC_000011.9:g.62387966T>C, NC_000011.9(NM_012200.3):c.257+3A>G (B3GAT3))

Chromosome 11
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.62387966T>C
DNA change (hg38) g.62620494T>C
Published as B3GAT3(NM_012200.3):c.257+3A>G (p.?)
ISCN -
DB-ID B3GAT3_000018
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 17:05:57 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B3GAT3 NM_012200.3 ?/. - c.257+3A>G r.spl? p.?
GANAB NM_198335.3 ?/. - c.*5321A>G r.(=) p.(=)


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