Variant #0000655050 (NC_000004.11:g.103488202del, NM_001165412.1:c.314del (NFKB1))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.103488202del
DNA change (hg38) g.102567045del
Published as NFKB1(NM_003998.4):c.317delA (p.N106Ifs*21)
ISCN -
DB-ID NFKB1_000019
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +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.314del r.(?) p.(Asn105IlefsTer21)
NFKB1 NM_003998.3 +/. - c.317del r.(?) p.(Asn106IlefsTer21)


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