ClinVar Miner

List of variants in gene IL2RA studied for not specified

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_000417.3(IL2RA):c.583+58A>G rs942199 0.96794
NM_000417.3(IL2RA):c.368-18A>G rs942200 0.89589
NM_000417.3(IL2RA):c.655+52A>G rs10752175 0.86111
NM_000417.3(IL2RA):c.367+12A>T rs12358961 0.31345
NM_000417.3(IL2RA):c.256+109T>C rs2025345 0.31307
NM_000417.3(IL2RA):c.367+7G>C rs11256369 0.20897
NM_000417.3(IL2RA):c.795-92G>A rs7076103 0.15379
NM_000417.3(IL2RA):c.84G>A (p.Pro28=) rs2228150 0.08221
NM_000417.3(IL2RA):c.516C>T (p.His172=) rs2228149 0.05507
NM_000417.3(IL2RA):c.584-109C>T rs2274036 0.02125
NM_000417.3(IL2RA):c.711A>G (p.Thr237=) rs11256354 0.00053
NM_000417.3(IL2RA):c.332G>A (p.Ser111Asn) rs56054476 0.00031
NM_000417.3(IL2RA):c.117G>A (p.Met39Ile) rs146345652 0.00017
NM_000417.3(IL2RA):c.484G>A (p.Gly162Ser) rs146966522 0.00015
NM_000417.3(IL2RA):c.655+4C>T rs373973017 0.00015
NM_000417.3(IL2RA):c.655+19G>A rs370895906 0.00011
NM_000417.3(IL2RA):c.457G>A (p.Val153Ile) rs201188114 0.00009
NM_000417.3(IL2RA):c.297A>T (p.Glu99Asp) rs201105599 0.00007
NM_000417.3(IL2RA):c.417T>G (p.Ile139Met) rs751445826 0.00006
NM_000417.3(IL2RA):c.643G>A (p.Val215Ile) rs145428184 0.00004
NM_000417.3(IL2RA):c.517G>A (p.Gly173Arg) rs752423140 0.00003
NM_000417.3(IL2RA):c.256+5_256+13del rs772838002 0.00002
NM_000417.3(IL2RA):c.788G>A (p.Arg263Gln) rs536344946 0.00002
NM_000417.3(IL2RA):c.554C>T (p.Thr185Ile) rs2132853580 0.00001
NM_000417.3(IL2RA):c.649A>G (p.Thr217Ala) rs757389911 0.00001
NM_000417.3(IL2RA):c.655+3G>A rs200818520 0.00001
NM_000417.3(IL2RA):c.107T>C (p.Phe36Ser) rs1839477553
NM_000417.3(IL2RA):c.193A>G (p.Met65Val) rs372359952
NM_000417.3(IL2RA):c.263G>A (p.Arg88Gln) rs139340259
NM_000417.3(IL2RA):c.263G>C (p.Arg88Pro) rs139340259
NM_000417.3(IL2RA):c.295G>C (p.Glu99Gln)
NM_000417.3(IL2RA):c.299A>G (p.Glu100Gly) rs1839442132
NM_000417.3(IL2RA):c.325A>G (p.Met109Val) rs1839441522
NM_000417.3(IL2RA):c.328C>A (p.Gln110Lys)
NM_000417.3(IL2RA):c.381A>T (p.Glu127Asp)
NM_000417.3(IL2RA):c.410A>G (p.Glu137Gly)
NM_000417.3(IL2RA):c.419A>T (p.Tyr140Phe) rs2132853878
NM_000417.3(IL2RA):c.548T>C (p.Ile183Thr)
NM_000417.3(IL2RA):c.616C>T (p.Arg206Cys) rs1438968487
NM_000417.3(IL2RA):c.701T>C (p.Ile234Thr)
NM_000417.3(IL2RA):c.98A>T (p.His33Leu) rs761518137

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