Variant #0000977156 (NC_000006.11:g.31639004T>C, NM_001320.5:c.*1301T>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.31639004T>C
DNA change (hg38) -
Published as LY6G5B(NM_021221.2):c.130T>C (p.(Ser44Pro))
ISCN -
DB-ID CSNK2B_000025
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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
CSNK2B NM_001320.5 ?/. - c.*1301T>C r.(=) p.(=)
LY6G5B NM_021221.2 ?/. - c.130T>C r.(?) p.(Ser44Pro)
GPANK1 NM_033177.3 ?/. - c.-6486A>G r.(?) p.(=)


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