Variant #0000534829 (NC_000008.10:g.42183529G>A, NM_001556.2:c.2028G>A (IKBKB))

Chromosome 8
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.42183529G>A
DNA change (hg38) g.42326011G>A
Published as IKBKB(NM_001190720.2):c.2022G>A (p.(Met674Ile)), IKBKB(NM_001556.3):c.2028G>A (p.M676I)
ISCN -
DB-ID IKBKB_000014 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) 0.00148 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IKBKB NM_001556.2 -/. - c.2028G>A r.(?) p.(Met676Ile)


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