Variant #0000506000 (NC_000001.10:g.235628971_235628972dup, NM_152490.3:c.824_825dup (B3GALNT2))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.235628971_235628972dup
DNA change (hg38) g.235465654_235465655dup
Published as B3GALNT2(NM_152490.3):c.824_825dupTT (p.(Ile276fs)), B3GALNT2(NM_152490.4):c.824_825dupTT (p.I276Lfs*26), B3GALNT2(NM_152490.5):c.824_825dupTT (p....)
ISCN -
DB-ID TBCE_000059 See all 2 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBCE NM_003193.3 +?/. - c.*16894_*16895dup r.(=) p.(=)
B3GALNT2 NM_152490.3 +?/. - c.824_825dup r.(?) p.(Ile276LeufsTer26)


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