Variant #0000689183 (NC_000004.11:g.103500059G>A, NM_001165412.1:c.590G>A (NFKB1))

Chromosome 4
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.103500059G>A
DNA change (hg38) -
Published as NFKB1(NM_001165412.1):c.590G>A (p.R197H)
ISCN -
DB-ID NFKB1_000023
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) 0.00044 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 2020-09-15 15:50:26 +02:00 (CEST)
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     
NFKB1 NM_001165412.1 -?/. - c.590G>A r.(?) p.(Arg197His)
NFKB1 NM_003998.3 -?/. - c.593G>A r.(?) p.(Arg198His)


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