Variant #0000548126 (NC_000012.11:g.44172041C>T, NM_001114182.2:c.877C>T (IRAK4))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44172041C>T
DNA change (hg38) g.43778238C>T
Published as IRAK4(NM_001351338.2):c.505C>T (p.Q169*), IRAK4(NM_016123.3):c.877C>T (p.Q293*)
ISCN -
DB-ID IRAK4_000007 See all 3 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) 0.00024 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IRAK4 NM_001114182.2 +/. - c.877C>T r.(?) p.(Gln293Ter)


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