Variant #0000857346 (NC_000001.10:g.235543465G>A, NM_152490.3:c.*70056C>T (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.235543465G>A
DNA change (hg38) -
Published as TBCE(NM_001079515.1):c.100+1G>A (p.?)
ISCN -
DB-ID TBCE_000097
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) 8.0E-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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBCE NM_003193.3 +?/. - c.100+1G>A r.spl? p.?
B3GALNT2 NM_152490.3 +?/. - c.*70056C>T r.(=) p.(=)


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