Variant #0000538959 (NC_000010.10:g.104160434A>G, NM_001077494.2:c.1821= (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.104160434A>G
DNA change (hg38) g.102400677A>G
Published as NFKB2(NM_001288724.1):c.1821A>G (p.A607=)
ISCN -
DB-ID FBXL15_000005 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) 0.9972 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFKB2 NM_001077494.2 -/. - c.1821= r.(=) p.(Ala607=)
PSD NM_001270965.1 -/. - c.*2523T>C r.(=) p.(=)
FBXL15 NM_024326.3 -/. - c.-20453A>G r.(?) p.(=)


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