Variant #0000719672 (NC_000004.11:g.103517382T>C, NM_001165412.1:c.1385T>C (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.103517382T>C
DNA change (hg38) -
Published as NFKB1(NM_003998.4):c.1388T>C (p.I463T)
ISCN -
DB-ID NFKB1_000025
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) 0.0002 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +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.1385T>C r.(?) p.(Ile462Thr)
NFKB1 NM_003998.3 -?/. - c.1388T>C r.(?) p.(Ile463Thr)


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