Variant #0000861801 (NC_000010.10:g.104159139G>T, NM_001077494.2:c.1212G>T (NFKB2))

Chromosome 10
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.104159139G>T
DNA change (hg38) -
Published as NFKB2(NM_001288724.1):c.1212G>T (p.G404=)
ISCN -
DB-ID FBXL15_000018
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) 0.00396 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFKB2 NM_001077494.2 -/. - c.1212G>T r.(?) p.(Gly404=)
PSD NM_001270965.1 -/. - c.*3818C>A r.(=) p.(=)
FBXL15 NM_024326.3 -/. - c.-21748G>T r.(?) p.(=)


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