Variant #0000521052 (NC_000004.11:g.103505961C>T, NM_001165412.1:c.1047C>T (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.103505961C>T
DNA change (hg38) g.102584804C>T
Published as NFKB1(NM_001165412.1):c.1047C>T (p.(Tyr349=))
ISCN -
DB-ID NFKB1_000009
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) 0.01529 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 2019-07-18 18:22:55 +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.1047C>T r.(?) p.(Tyr349=)
NFKB1 NM_003998.3 -?/. - c.1050C>T r.(?) p.(Tyr350=)


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