Variant #0000521058 (NC_000004.11:g.103533226C>G, NM_001165412.1:c.2375C>G (NFKB1))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.103533226C>G
DNA change (hg38) g.102612069C>G
Published as NFKB1(NM_003998.4):c.2378C>G (p.P793R)
ISCN -
DB-ID NFKB1_000015
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) 4.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFKB1 NM_001165412.1 ?/. - c.2375C>G r.(?) p.(Pro792Arg)
NFKB1 NM_003998.3 ?/. - c.2378C>G r.(?) p.(Pro793Arg)


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