Variant #0000566564 (NC_000019.9:g.17918784_17918785del, NM_014256.3:c.168_169del (B3GNT3))

Chromosome 19
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.17918784_17918785del
DNA change (hg38) g.17807975_17807976del
Published as B3GNT3(NM_014256.3):c.168_169del (p.(Ala57ProfsTer45))
ISCN -
DB-ID B3GNT3_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) 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 2020-07-15 15:39:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
B3GNT3 NM_014256.3 -?/. - c.168_169del r.(?) p.(Ala57ProfsTer45)


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