Variant #0001000002 (NC_000012.11:g.44166106G>C, NM_001114182.2:c.431G>C (IRAK4))

Chromosome 12
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.44166106G>C
DNA change (hg38) -
Published as IRAK4(NM_001351338.1):c.59G>C (p.S20T), IRAK4(NM_016123.3):c.431G>C (p.(Ser144Thr))
ISCN -
DB-ID IRAK4_000018 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
IRAK4 NM_001114182.2 -?/. - c.431G>C r.(?) p.(Ser144Thr)


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