Variant #0000888359 (NC_000008.10:g.42173806G>A, NM_001556.2:c.879G>A (IKBKB))

Chromosome 8
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.42173806G>A
DNA change (hg38) -
Published as IKBKB(NM_001242778.1):c.702G>A (p.T234=), IKBKB(NM_001556.3):c.879G>A (p.T293=)
ISCN -
DB-ID IKBKB_000028 See all 2 reported entries
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) 0.00021 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IKBKB NM_001556.2 -?/. - c.879G>A r.(?) p.(Thr293=)


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