Variant #0000949734 (NC_000011.9:g.62389419T>A, NM_012200.3:c.1A>T (B3GAT3))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.62389419T>A
DNA change (hg38) -
Published as B3GAT3(NM_001288721.1):c.-260A>T (p.(=)), B3GAT3(NM_001288723.1):c.1A>T (p.M1?), B3GAT3(NM_012200.4):c.1A>T (p.M1?)
ISCN -
DB-ID B3GAT3_000022 See all 4 reported entries
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) 2.0E-5 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B3GAT3 NM_012200.3 +/. - c.1A>T r.(?) p.(Met1?)
GANAB NM_198335.3 +/. - c.*3868A>T r.(=) p.(=)


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