Variant #0000330886 (NC_000006.11:g.31626904C>G, NM_001320.5:c.-7093C>G (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.31626904C>G
DNA change (hg38) g.31659127C>G
Published as C6orf47(NM_021184.3):c.821G>C (p.(Trp274Ser))
ISCN -
DB-ID C6orf47_000001
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) 0.00187 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSNK2B NM_001320.5 ?/. - c.-7093C>G r.(?) p.(=)
APOM NM_019101.2 ?/. - c.*1038C>G r.(=) p.(=)
C6orf47 NM_021184.3 ?/. - c.821G>C r.(?) p.(Trp274Ser)
GPANK1 NM_033177.3 ?/. - c.*3139G>C r.(=) p.(=)
BAG6 NM_080703.2 ?/. - c.-6741G>C r.(?) p.(=)


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