List of variants in gene IRAK4 reported as benign for Immunodeficiency 67

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_016123.4(IRAK4):c.*2188A>G	rs1141168	0.42335
NM_016123.4(IRAK4):c.*1794T>C	rs4251555	0.23988
NM_016123.4(IRAK4):c.*2433T>C	rs9849	0.21802
NM_016123.4(IRAK4):c.1282G>A (p.Ala428Thr)	rs4251545	0.15022
NM_016123.4(IRAK4):c.*1895G>A	rs4251558	0.06270
NM_016123.4(IRAK4):c.*1887C>T	rs4251556	0.05478
NM_016123.4(IRAK4):c.*623A>G	rs4251552	0.04621
NM_016123.4(IRAK4):c.*2704C>T	rs4251562	0.01948
NM_016123.4(IRAK4):c.*1760G>A	rs144535012	0.01652
NM_016123.4(IRAK4):c.*146T>C	rs4251546	0.01572
NM_016123.4(IRAK4):c.*608A>G	rs4251551	0.01257
NM_016123.4(IRAK4):c.*2761G>A	rs4251563	0.01239
NM_016123.4(IRAK4):c.*270C>T	rs4251547	0.01024
NM_016123.4(IRAK4):c.1172G>A (p.Arg391His)	rs55944915	0.00992
NM_016123.4(IRAK4):c.*1777A>T	rs4251554	0.00905
NM_016123.4(IRAK4):c.*2083C>G	rs111813306	0.00814
NM_016123.4(IRAK4):c.1126-19A>T	rs11182263	0.00802
NM_016123.4(IRAK4):c.307+18A>G	rs118097313	0.00685
NM_016123.4(IRAK4):c.941+18A>G	rs11182261	0.00683
NM_016123.4(IRAK4):c.318C>G (p.Pro106=)	rs56338336	0.00520
NM_016123.4(IRAK4):c.*1272G>T	rs182497864	0.00517
NM_016123.4(IRAK4):c.117T>A (p.Ile39=)	rs141039652	0.00083
NM_016123.4(IRAK4):c.*1325G>A	rs139778399	0.00029
NM_016123.4(IRAK4):c.490+16A>C	rs186000885	0.00011
NM_016123.4(IRAK4):c.1126-11dup	rs753200898
NM_016123.4(IRAK4):c.1126-18T>A	rs144296954

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