Variant #0000528260 (NC_000006.11:g.31630171G>A, NM_001320.5:c.-3826G>A (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.31630171G>A
DNA change (hg38) g.31662394G>A
Published as GPANK1(NM_001199237.1):c.943C>T (p.(Arg315Ter))
ISCN -
DB-ID APOM_000003
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) 4.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-18 16:43:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSNK2B NM_001320.5 ?/. - c.-3826G>A r.(?) p.(=)
APOM NM_019101.2 ?/. - c.*4305G>A r.(=) p.(=)
C6orf47 NM_021184.3 ?/. - c.-2447C>T r.(?) p.(=)
GPANK1 NM_033177.3 ?/. - c.943C>T r.(?) p.(Arg315Ter)
BAG6 NM_080703.2 ?/. - c.-10008C>T r.(?) p.(=)


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