ClinVar Miner

List of variants in gene IL2RA reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_000417.3(IL2RA):c.*471G>A rs553112485 0.00118
NM_000417.3(IL2RA):c.*1041C>T rs141524746 0.00113
NM_000417.3(IL2RA):c.*1044T>C rs572589682 0.00066
NM_000417.3(IL2RA):c.656-14T>A rs74162097 0.00053
NM_000417.3(IL2RA):c.*1186C>T rs12722603 0.00043
NM_000417.3(IL2RA):c.*444T>A rs12722601 0.00042
NM_000417.3(IL2RA):c.757G>A (p.Val253Ile) rs143550766 0.00035
NM_000417.3(IL2RA):c.*2131A>G rs549245031 0.00033
NM_000417.3(IL2RA):c.332G>A (p.Ser111Asn) rs56054476 0.00033
NM_000417.3(IL2RA):c.*963A>C rs527589024 0.00027
NM_000417.3(IL2RA):c.*2055T>C rs561032746 0.00024
NM_000417.3(IL2RA):c.*599C>G rs541601070 0.00024
NM_000417.3(IL2RA):c.*889G>A rs147669116 0.00016
NM_000417.3(IL2RA):c.*1974C>T rs12722720 0.00015
NM_000417.3(IL2RA):c.655+4C>T rs373973017 0.00015
NM_000417.3(IL2RA):c.*2178T>A rs886047070 0.00014
NM_000417.3(IL2RA):c.787C>T (p.Arg263Trp) rs140088691 0.00009
NM_000417.3(IL2RA):c.*1766T>C rs961187614 0.00008
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.*1500T>C rs894358573 0.00006
NM_000417.3(IL2RA):c.584-6C>T rs201675947 0.00006
NM_000417.3(IL2RA):c.427G>A (p.Val143Met) rs886047082 0.00004
NM_000417.3(IL2RA):c.*103C>T rs886047080 0.00003
NM_000417.3(IL2RA):c.*1042G>A rs542812308 0.00003
NM_000417.3(IL2RA):c.*1574C>T rs886047073 0.00003
NM_000417.3(IL2RA):c.*93G>A rs886047081 0.00003
NM_000417.3(IL2RA):c.732C>T (p.Ala244=) rs779403244 0.00003
NM_000417.3(IL2RA):c.669G>A (p.Gln223=) rs539966138 0.00002
NM_000417.3(IL2RA):c.*1084C>T rs1305512354 0.00001
NM_000417.3(IL2RA):c.*1454A>G rs886047075 0.00001
NM_000417.3(IL2RA):c.*1650G>A rs886047071 0.00001
NM_000417.3(IL2RA):c.*2144T>G rs757107768 0.00001
NM_000417.3(IL2RA):c.*767C>T rs143416542 0.00001
NM_000417.3(IL2RA):c.167G>A (p.Arg56His) rs886047083 0.00001
NM_000417.3(IL2RA):c.252C>T (p.Ser84=) rs1034684102 0.00001
NM_000417.3(IL2RA):c.*1026G>T rs28360484
NM_000417.3(IL2RA):c.*1154_*1158dup rs543983290
NM_000417.3(IL2RA):c.*1426G>A rs1589287690
NM_000417.3(IL2RA):c.*1443G>C rs946697468
NM_000417.3(IL2RA):c.*1539T>C rs886047074
NM_000417.3(IL2RA):c.*1575G>A rs886047072
NM_000417.3(IL2RA):c.*1619G>A rs773626989
NM_000417.3(IL2RA):c.*1643C>A rs1839186433
NM_000417.3(IL2RA):c.*261A>G rs1784639100
NM_000417.3(IL2RA):c.*410_*411del rs886047079
NM_000417.3(IL2RA):c.*414C>T rs886047078
NM_000417.3(IL2RA):c.*513T>C rs1839203302
NM_000417.3(IL2RA):c.*672A>G rs886047077
NM_000417.3(IL2RA):c.*676C>T rs566194606
NM_000417.3(IL2RA):c.*884C>T rs886047076
NM_000417.3(IL2RA):c.*895T>A rs1589287979
NM_000417.3(IL2RA):c.256+1G>A rs1564543963
NM_000417.3(IL2RA):c.257-11A>G rs929482812
NM_000417.3(IL2RA):c.328C>G (p.Gln110Glu) rs1839441418
NM_000417.3(IL2RA):c.678G>T (p.Met226Ile) rs1839342849
NM_000417.3(IL2RA):c.693G>C (p.Glu231Asp) rs139266750
NM_000417.3(IL2RA):c.76G>C (p.Asp26His) rs55868253
NM_000417.3(IL2RA):c.777C>A (p.Leu259=) rs554680869

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