Variant #0000910981 (NC_000001.10:g.235597525C>T, NM_152490.3:c.*15996G>A (B3GALNT2))

Chromosome 1
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.235597525C>T
DNA change (hg38) -
Published as TBCE(NM_001079515.1):c.667C>T (p.(Arg223Trp)), TBCE(NM_001079515.2):c.667C>T (p.R223W)
ISCN -
DB-ID TBCE_000018 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) 0.00062 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 2023-01-11 15:44:22 +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.667C>T r.(?) p.(Arg223Trp)
B3GALNT2 NM_152490.3 -?/. - c.*15996G>A r.(=) p.(=)


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