Variant #0000970173 (NC_000020.10:g.472838del, NC_000020.10(NM_177559.2):c.621+71del (CSNK2A1))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.472838del
DNA change (hg38) g.492194del
Published as CSNK2A1(NM_001895.4):c.621+71delA
ISCN -
DB-ID CSNK2A1_000022
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 2024-02-26 20:06:56 +01:00 (CET)
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.621+71del r.(?) p.(=)


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