Variant #0001053692 (NC_000010.10:g.104160728A>T, NM_001077494.2:c.1993A>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.104160728A>T
DNA change (hg38) -
Published as NFKB2(NM_001077494.3):c.1993A>T (p.T665S), NFKB2(NM_001322934.2):c.1993A>T (p.(Thr665Ser))
ISCN -
DB-ID FBXL15_000026 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) 7.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
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.1993A>T r.(?) p.(Thr665Ser)
PSD NM_001270965.1 -?/. - c.*2229T>A r.(=) p.(=)
FBXL15 NM_024326.3 -?/. - c.-20159A>T r.(?) p.(=)


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