Variant #0000655052 (NC_000004.11:g.103533702_103533706dup, NM_001165412.1:c.2528_2532dup (NFKB1))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.103533702_103533706dup
DNA change (hg38) g.102612545_102612549dup
Published as NFKB1(NM_001165412.1):c.2528_2532dupTACTT (p.N845Yfs*8)
ISCN -
DB-ID NFKB1_000021
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
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.2528_2532dup r.(?) p.(Asn845TyrfsTer8)
NFKB1 NM_003998.3 +?/. - c.2531_2535dup r.(?) p.(Asn846TyrfsTer8)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.