Variant #0000608950 (NC_000004.11:g.103522150G>A, NM_001165412.1:c.1733G>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.103522150G>A
DNA change (hg38) g.102600993G>A
Published as NFKB1(NM_003998.4):c.1736G>A (p.R579K)
ISCN -
DB-ID NFKB1_000018 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) 0.00155 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 2019-12-04 14:54:23 +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     
NFKB1 NM_001165412.1 -?/. - c.1733G>A r.(?) p.(Arg578Lys)
NFKB1 NM_003998.3 -?/. - c.1736G>A r.(?) p.(Arg579Lys)


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