Variant #0000809262 (NC_000020.10:g.467035C>T, NM_177559.2:c.1045G>A (CSNK2A1))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.467035C>T
DNA change (hg38) g.486391C>T
Published as CSNK2A1(NM_001895.4):c.1045G>A (p.A349T)
ISCN -
DB-ID CSNK2A1_000019
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) 0.00011 View details
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 2025-02-14 12:35:55 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSNK2A1 NM_177559.2 -?/. - c.1045G>A r.(?) p.(Ala349Thr)


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