Variant #0000717276 (NC_000001.10:g.235582786A>T, NM_152490.3:c.*30735T>A (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.235582786A>T
DNA change (hg38) -
Published as TBCE(NM_003193.5):c.372-2A>T
ISCN -
DB-ID TBCE_000088
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +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     
TBCE NM_003193.3 +?/. - c.372-2A>T r.spl? p.?
B3GALNT2 NM_152490.3 +?/. - c.*30735T>A r.(=) p.(=)


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