Variant #0000883226 (NC_000001.10:g.235602180A>G, NM_152490.3:c.*11341T>C (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.235602180A>G
DNA change (hg38) -
Published as TBCE(NM_001079515.1):c.1213A>G (p.(Asn405Asp))
ISCN -
DB-ID TBCE_000100
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 2022-11-01 13:01:21 +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.1213A>G r.(?) p.(Asn405Asp)
B3GALNT2 NM_152490.3 -?/. - c.*11341T>C r.(=) p.(=)


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