Variant #0000848584 (NC_000001.10:g.235543508_235543529del, NM_152490.3:c.*70023_*70044del (B3GALNT2))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.235543508_235543529del
DNA change (hg38) -
Published as TBCE(NM_001079515.2):c.100+44_100+65delGTGTGTGTGTGTGTGTGTGTGT, TBCE(NM_001287801.2):c.100+44_100+65delGTGTGTGTGTGTGTGTGTGTGT
ISCN -
DB-ID TBCE_000005 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBCE NM_003193.3 -/. - c.100+44_100+65del r.(=) p.(=)
B3GALNT2 NM_152490.3 -/. - c.*70023_*70044del r.(=) p.(=)


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