Variant #0000268012 (NC_000015.9:g.40488858_40488860del, NM_001211.5:c.1171_1173del (BUB1B))

Chromosome 15
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.40488858_40488860del
DNA change (hg38) g.40196657_40196659del
Published as BUB1B(NM_001211.6):c.1171_1173del (p.(Glu391del)), BUB1B(NM_001211.6):c.1171_1173delGAG (p.E391del)
ISCN -
DB-ID BUB1B_000008 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BUB1B NM_001211.5 ?/. - c.1171_1173del r.(?) p.(Glu391del)


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