Variant #0001050478 (NC_000001.10:g.235647632G>A, NC_000001.10(NM_152490.3):c.555+6C>T (B3GALNT2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.235647632G>A
DNA change (hg38) -
Published as B3GALNT2(NM_152490.5):c.555+6C>T
ISCN -
DB-ID TBCE_000117
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBCE NM_003193.3 ?/. - c.*35555G>A r.(=) p.(=)
B3GALNT2 NM_152490.3 ?/. - c.555+6C>T r.(=) p.(=)


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