Variant #0000505981 (NC_000001.10:g.235577894_235577899del, NM_152490.3:c.*35622_*35627del (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.235577894_235577899del
DNA change (hg38) g.235414579_235414584del
Published as TBCE(NM_001287801.2):c.332_337delTGGAGA (p.V111_T113delinsA)
ISCN -
DB-ID TBCE_000045
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBCE NM_003193.3 ?/. - c.332_337del r.(?) p.(Val111_Thr113delinsAla)
B3GALNT2 NM_152490.3 ?/. - c.*35622_*35627del r.(=) p.(=)


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