Variant #0000857349 (NC_000001.10:g.235602193A>G, NM_152490.3:c.*11328T>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.235602193A>G
DNA change (hg38) -
Published as TBCE(NM_001079515.1):c.1226A>G (p.(Glu409Gly)), TBCE(NM_001079515.2):c.1226A>G (p.E409G), TBCE(NM_001287801.2):c.1379A>G (p.E460G)
ISCN -
DB-ID TBCE_000029 See all 3 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) 0.00587 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.1226A>G r.(?) p.(Glu409Gly)
B3GALNT2 NM_152490.3 -?/. - c.*11328T>C r.(=) p.(=)


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