Variant #0000888356 (NC_000008.10:g.42129597A>G, NC_000008.10(NM_001556.2):c.-18-4A>G (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.42129597A>G
DNA change (hg38) -
Published as IKBKB(NM_001242778.1):c.-100-4A>G (p.(=)), IKBKB(NM_001556.3):c.-18-4A>G
ISCN -
DB-ID IKBKB_000002 See all 3 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) 0.00082 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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IKBKB NM_001556.2 -?/. - c.-18-4A>G r.spl? p.?


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