Variant #0000682244 (NC_000023.10:g.153278550G>A, NM_001569.3:c.1874C>T (IRAK1))

Chromosome X
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.153278550G>A
DNA change (hg38) -
Published as IRAK1(NM_001569.3):c.1874C>T (p.T625M), IRAK1(NM_001569.4):c.1874C>T (p.T625M)
ISCN -
DB-ID IRAK1_000042 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) 0.00397 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IRAK1 NM_001569.3 -?/. - c.1874C>T r.(?) p.(Thr625Met)


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