Variant #0000888973 (NC_000010.10:g.104161671C>T, NM_001077494.2:c.2463C>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.104161671C>T
DNA change (hg38) -
Published as NFKB2(NM_001288724.1):c.2463C>T (p.Y821=)
ISCN -
DB-ID FBXL15_000023
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) Retrieve
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFKB2 NM_001077494.2 -/. - c.2463C>T r.(?) p.(Tyr821=)
PSD NM_001270965.1 -/. - c.*1286G>A r.(=) p.(=)
FBXL15 NM_024326.3 -/. - c.-19216C>T r.(?) p.(=)


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