List of variants in gene IL2RA reported as likely benign for immune system disorder

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: 93

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HGVS	dbSNP	gnomAD frequency
NM_000417.3(IL2RA):c.*752A>G	rs41290329	0.00754
NM_000417.3(IL2RA):c.*107C>T	rs12722714	0.00417
NM_000417.3(IL2RA):c.*1061C>T	rs55885853	0.00404
NM_000417.3(IL2RA):c.*888C>T	rs12722716	0.00239
NM_000417.3(IL2RA):c.272C>T (p.Thr91Met)	rs72650666	0.00183
NM_000417.3(IL2RA):c.691G>C (p.Glu231Gln)	rs150060415	0.00059
NM_000417.3(IL2RA):c.656-14T>A	rs74162097	0.00053
NM_000417.3(IL2RA):c.357G>A (p.Ala119=)	rs150164762	0.00034
NM_000417.3(IL2RA):c.*1772A>C	rs74973937	0.00028
NM_000417.3(IL2RA):c.656-4A>G	rs114399155	0.00016
NM_000417.3(IL2RA):c.342G>A (p.Gln114=)	rs376596128	0.00014
NM_000417.3(IL2RA):c.655+19G>A	rs370895906	0.00011
NM_000417.3(IL2RA):c.584-11C>T	rs750468923	0.00008
NM_000417.3(IL2RA):c.693G>A (p.Glu231=)	rs139266750	0.00008
NM_000417.3(IL2RA):c.756C>T (p.Ser252=)	rs113428577	0.00008
NM_000417.3(IL2RA):c.204A>G (p.Thr68=)	rs563759672	0.00007
NM_000417.3(IL2RA):c.279A>G (p.Gln93=)	rs773086693	0.00006
NM_000417.3(IL2RA):c.584-6C>T	rs201675947	0.00006
NM_000417.3(IL2RA):c.655+15A>C	rs377051679	0.00006
NM_000417.3(IL2RA):c.*183C>A	rs542942584	0.00004
NM_000417.3(IL2RA):c.367+10G>A	rs767262856	0.00004
NM_000417.3(IL2RA):c.609C>T (p.Pro203=)	rs760357500	0.00004
NM_000417.3(IL2RA):c.795-16T>C	rs548889439	0.00003
NM_000417.3(IL2RA):c.813A>G (p.Thr271=)	rs775980513	0.00003
NM_000417.3(IL2RA):c.669G>A (p.Gln223=)	rs539966138	0.00002
NM_000417.3(IL2RA):c.696G>A (p.Thr232=)	rs762837534	0.00002
NM_000417.3(IL2RA):c.768G>A (p.Leu256=)	rs755034813	0.00002
NM_000417.3(IL2RA):c.222G>A (p.Ser74=)	rs751234465	0.00001
NM_000417.3(IL2RA):c.252C>T (p.Ser84=)	rs1034684102	0.00001
NM_000417.3(IL2RA):c.256+7G>A	rs368269963	0.00001
NM_000417.3(IL2RA):c.456C>T (p.Cys152=)	rs377104035	0.00001
NM_000417.3(IL2RA):c.584-7C>T	rs1467786063	0.00001
NM_000417.3(IL2RA):c.584-8del	rs748515506	0.00001
NM_000417.3(IL2RA):c.606C>T (p.Ser202=)	rs763179568	0.00001
NM_000417.3(IL2RA):c.75C>T (p.Asp25=)	rs547040700	0.00001
NM_000417.3(IL2RA):c.99C>T (p.His33=)	rs1404900373	0.00001
NM_000417.3(IL2RA):c.*1026G>A	rs28360484
NM_000417.3(IL2RA):c.153C>T (p.Cys51=)	rs907714536
NM_000417.3(IL2RA):c.189C>G (p.Leu63=)	rs2132859295
NM_000417.3(IL2RA):c.225C>G (p.Ser75=)	rs372481445
NM_000417.3(IL2RA):c.237A>G (p.Gln79=)
NM_000417.3(IL2RA):c.246C>T (p.Cys82=)
NM_000417.3(IL2RA):c.256+10C>T	rs2132859141
NM_000417.3(IL2RA):c.256+14C>T
NM_000417.3(IL2RA):c.257-11A>G	rs929482812
NM_000417.3(IL2RA):c.257-14T>C	rs2132857309
NM_000417.3(IL2RA):c.257-20A>G
NM_000417.3(IL2RA):c.273G>A (p.Thr91=)
NM_000417.3(IL2RA):c.282G>A (p.Val94=)	rs774606930
NM_000417.3(IL2RA):c.285A>T (p.Thr95=)
NM_000417.3(IL2RA):c.321A>C (p.Thr107=)	rs1839441567
NM_000417.3(IL2RA):c.360C>T (p.Ser120=)
NM_000417.3(IL2RA):c.367+18C>T
NM_000417.3(IL2RA):c.367+9T>A	rs1039385689
NM_000417.3(IL2RA):c.367+9T>C
NM_000417.3(IL2RA):c.368-19_368-18delinsAG	rs2132854087
NM_000417.3(IL2RA):c.368-19_368-18inv
NM_000417.3(IL2RA):c.368-4C>T
NM_000417.3(IL2RA):c.368-8T>C	rs2132854050
NM_000417.3(IL2RA):c.468C>T (p.Tyr156=)
NM_000417.3(IL2RA):c.495G>A (p.Glu165=)	rs776347887
NM_000417.3(IL2RA):c.498C>T (p.Ser166=)	rs747017654
NM_000417.3(IL2RA):c.525A>C (p.Thr175=)
NM_000417.3(IL2RA):c.583+10C>T	rs2132853534
NM_000417.3(IL2RA):c.583+19G>A
NM_000417.3(IL2RA):c.584-10T>C
NM_000417.3(IL2RA):c.584-12TC[4]	rs774599486
NM_000417.3(IL2RA):c.639C>T (p.Cys213=)
NM_000417.3(IL2RA):c.642C>T (p.Leu214=)
NM_000417.3(IL2RA):c.645C>G (p.Val215=)	rs1839354112
NM_000417.3(IL2RA):c.65-10T>G
NM_000417.3(IL2RA):c.65-16T>G
NM_000417.3(IL2RA):c.65-18G>C
NM_000417.3(IL2RA):c.655+18C>T
NM_000417.3(IL2RA):c.656-11_656-10del	rs780223643
NM_000417.3(IL2RA):c.656-12T>A
NM_000417.3(IL2RA):c.714G>A (p.Glu238=)
NM_000417.3(IL2RA):c.727+10G>C
NM_000417.3(IL2RA):c.727+19T>C	rs2132850272
NM_000417.3(IL2RA):c.727+9G>A
NM_000417.3(IL2RA):c.728-10C>G
NM_000417.3(IL2RA):c.728-12C>G
NM_000417.3(IL2RA):c.728-12C>T
NM_000417.3(IL2RA):c.728-16CT[3]
NM_000417.3(IL2RA):c.728-8A>G
NM_000417.3(IL2RA):c.747G>A (p.Leu249=)	rs2132848239
NM_000417.3(IL2RA):c.777C>A (p.Leu259=)	rs554680869
NM_000417.3(IL2RA):c.794+10G>A
NM_000417.3(IL2RA):c.794+10G>C	rs2132848057
NM_000417.3(IL2RA):c.794+16C>G
NM_000417.3(IL2RA):c.795-7A>G	rs750285734
NM_000417.3(IL2RA):c.807A>G (p.Arg269=)
NM_000417.3(IL2RA):c.81C>T (p.Asp27=)

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