Variant #0000521054 (NC_000004.11:g.103514741T>C, NC_000004.11(NM_001165412.1):c.1207+16T>C (NFKB1))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.103514741T>C
DNA change (hg38) g.102593584T>C
Published as NFKB1(NM_003998.4):c.1210+16T>C
ISCN -
DB-ID NFKB1_000011
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) 0.35803 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.1207+16T>C r.(=) p.(=)
NFKB1 NM_003998.3 -/. - c.1210+16T>C r.(=) p.(=)


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