Variant #0000528262 (NC_000006.11:g.31635733T>A, NM_001320.5:c.161T>A (CSNK2B))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31635733T>A
DNA change (hg38) g.31667956T>A
Published as CSNK2B(NM_001320.7):c.161T>A (p.L54*)
ISCN -
DB-ID CSNK2B_000012
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 2019-07-18 18:22:55 +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     
CSNK2B NM_001320.5 +?/. - c.161T>A r.(?) p.(Leu54Ter)
LY6G5B NM_021221.2 +?/. - c.-2995T>A r.(?) p.(=)
GPANK1 NM_033177.3 +?/. - c.-3215A>T r.(?) p.(=)


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