Variant #0000888969 (NC_000010.10:g.104158628G>T, NC_000010.10(NM_001077494.2):c.1117+7G>T (NFKB2))

Chromosome 10
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.104158628G>T
DNA change (hg38) -
Published as NFKB2(NM_001077494.2):c.1117+7G>T (p.(=)), NFKB2(NM_001288724.1):c.1117+7G>T
ISCN -
DB-ID NFKB2_000003 See all 2 reported entries
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) 0.00037 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFKB2 NM_001077494.2 -?/. - c.1117+7G>T r.(=) p.(=)
PSD NM_001270965.1 -?/. - c.*4329C>A r.(=) p.(=)
FBXL15 NM_024326.3 -?/. - c.-22259G>T r.(?) p.(=)


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