Variant #0001052296 (NC_000006.11:g.31637092C>A, NC_000006.11(NM_001320.5):c.368-4C>A (CSNK2B))

Chromosome 6
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.31637092C>A
DNA change (hg38) -
Published as CSNK2B(NM_001320.7):c.368-4C>A
ISCN -
DB-ID CSNK2B_000030
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSNK2B NM_001320.5 ?/. - c.368-4C>A r.spl? p.?
LY6G5B NM_021221.2 ?/. - c.-1636C>A r.(?) p.(=)
GPANK1 NM_033177.3 ?/. - c.-4574G>T r.(?) p.(=)


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