Variant #0000995652 (NC_000006.11:g.31637676dup, NM_001320.5:c.621dup (CSNK2B))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31637676dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID CSNK2B_000011 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSNK2B NM_001320.5 +/. - c.621dup r.(?) p.(Lys208Glnfs*38)
LY6G5B NM_021221.2 +/. - c.-1052dup r.(?) p.(=)
GPANK1 NM_033177.3 +/. - c.-5158dup r.(?) p.(=)


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