Variant #0000863801 (NC_000015.9:g.40512803G>A, NM_001211.5:c.2996G>A (BUB1B))

Chromosome 15
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.40512803G>A
DNA change (hg38) -
Published as BUB1B(NM_001211.5):c.2996G>A (p.R999Q)
ISCN -
DB-ID BUB1B_000036
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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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     
PAK6 NM_001128628.1 -?/. - c.-201+2935G>A r.(=) p.(=)
BUB1B NM_001211.5 -?/. - c.2996G>A r.(?) p.(Arg999Gln)


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