Variant #0000802483 (NC_000006.11:g.31637285G>C, NM_001320.5:c.557G>C (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.31637285G>C
DNA change (hg38) -
Published as CSNK2B(NM_001320.7):c.557G>C (p.R186T)
ISCN -
DB-ID CSNK2B_000017
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.557G>C r.(?) p.(Arg186Thr)
LY6G5B NM_021221.2 ?/. - c.-1443G>C r.(?) p.(=)
GPANK1 NM_033177.3 ?/. - c.-4767C>G r.(?) p.(=)


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